REVIEW ARTICLE

Genetic polymorphisms and endometriosis: contribution of genes that regulate vascular function and tissue remodeling
Alessandra Bernadete Trov
de

Marqui

PhD Student in Genetics; Associate Professor of Genetics at Universidade Federal do Tringulo Mineiro, Uberaba, MG, Brazil

Summary
Endometriosis is a benign gynecological disease characterized by the presence and growth of endometrial cells outside the uterus. Genetic, endocrine, immunological, and environmental factors have been suggested in its pathogenesis. A great number of studies have related genetic polymorphisms as a factor that contributes to the development of endometriosis. This review presents a detailed description of the contribution of genetic polymorphisms in genes that regulate vascular function and tissue remodeling in endometriosis (alpha 2-HS glycoprotein [AHSG], epidermal growth factor receptor [EGFR], vascular endothelial growth factor [VEGF], endostatin, plasminogen activator inhibitor 1 [PAI-1], angiotensin I-converting enzyme [ACE], and matrix metalloproteinases [MMPs]). Some polymorphisms of the VEGF (-460 C/T, +405 G/C, +936 C/T), PAI, MMP-1, 2, and 3 genes were widely studied, while polymorphisms of the AHSG, EGF, endostatin, and VEGF (-1154 G/A, -2578 A/C) genes were not. In this latter case, additional studies are required to confirm the findings of the few studies that have analyzed these single nucleotide polymorphisms (SNPs). Additionally, studies that found a positive or negative association of SNP with endometriosis emphasize the relevance of studies with a large number of control cases to confirm their findings. The haplotype analysis was performed only for the VEGF (-460, +405, -1154 and -2578), ACE (-240/2350) and MMP-1, 2, 3, and 9 genes, and in most of them, there was no association with endometriosis. Of the eight works that analyzed haplotypes of the VEGF gene, five did not associate them with endometriosis. Haplotypes of ACE and MMP-2 genes were not associated with endometriosis, while those of MMP-1, 3, and 9 genes were related to a high risk for the disease. Keywords: Endometriosis; genetic polymorphisms; vascular endothelial growth factor; matrix metalloproteinases; plasminogen activator inhibitors; peptidyl dipeptidase A.
2012 Elsevier Editora Ltda. All rights reserved. Study conducted at Universidade Federal do Tringulo Mineiro, Uberaba, MG, Brazil

Submitted on: 12/13/2011 Approved on: 05/11/2012

Correspondence to: Alessandra Bernadete Trov de Marqui Instituto de Cincias Biolgicas e Naturais Disciplina de Gentica Campus I Praa Manoel Terra, 330 38015-050 Uberaba MG, Brazil [email protected] Conflict of interest: None.

620

Genetic polymorphisms

and endometriosis: contribution of genes that regulate vascular function and tissue remodeling

Introduction
Endometriosis is a complex gynecological condition characterized by endometrial tissue outside the uterus. Main clinical symptoms include dysmenorrhea, chronic pelvic pain, deep dyspareunia, infertility, and cyclic bowel and urinary symptoms, such as pain or bleeding when defecating/urinating during the menstrual period1,2. A study performed by Bellelis et al.3 showed that the main complaint reported by patients with endometriosis was dysmenorrhea, with a prevalence of 62.2%. Nonetheless, when all symptoms reported were considered, chronic pelvic pain was the most prevalent symptom, followed by deep dyspareunia, reported by 56.8% and 54.7% of the patients, respectively. Infertility was reported by 39.8% of the 892 patients. A study aiming at understanding the Brazilian gynecological practices regarding the diagnosis of endometriosis showed early detection of endometriosis when the patient complained of infertility or chronic pelvic pain4. An interesting finding of this study was that the time elapsed until indication of a diagnostic procedure was lower in case of doctors that had participated in congresses and lectures on gynecological endoscopy and endometriosis, thus evidencing that better-informed gynecologists detect the disease earlier4. Endometriosis is similar to cancer, as the implantation of endometrial cells requires neovascularization in order to establish, grow, and invade tissues. Additionally, theories on the etiopathogenesis of endometriosis involve growth factors and cytokines associated with the regulation of cell multiplication and neoangiogenesis that may act in carcinogenesis. It is estimated that 1% of endometriosis cases are related to cancer and, for some types of endometriosis, its benign nature has been questioned5,6. Although the final diagnosis of endometriosis requires needs a surgical intervention, videolaparoscopy, several findings in the physical, image, and laboratory examinations can already predict, with a high degree of reliability, that the patient has this disease. During this surgical procedure, it is possible to view lesions suggestive of the disease and to obtain a tissue sample for anatomopathological analysis and confirmation of the endometriosis diagnosis7. The classification used for endometriosis is that of the American Society of Reproductive Medicine/ASRM, revised in 1996, which classifies this disease into four stages: minimal (stage I), mild (stage II), moderate (stage III), or severe (stage IV)8. Currently, the most widespread treatments are surgery, ovarian suppression therapy, or the combination of both5,7. The cause of endometriosis remains unknown. Nonetheless, there are evidences of immunological9,10, environmental11, and genetic12-14 factors involved in its pathogenesis.

Regarding the immune response, the role of cytokines in the development of endometriosis15 is emphasized; high levels of many cytokines were found in patients with endometriosis16-18. The same group of researchers, in independent works, assessed the levels of cytokines involved in immune response patterns Th1 [interleukin (IL)-2, tumor necrosis factor (TNF)-alpha, and interferon (IFN)-gamma] and Th2 (IL-4 and IL-10) in patients with endometriosis (n=65) and in those without the disease (n=33)16-18. Podgaec et al. noted an increase in the levels of IFN-gamma and IL-10 in patients with endometriosis, evidencing the co-existence of both responses16. However, when considering the ratio between cytokine levels and these responses, there was a predominance of IL-4 and IL-10, thus reflecting a potential change of the Th2 immune response component. In the subsequent study, cytokine levels were associated with the clinical symptoms of endometriosis18. Patients with endometriosis that presented deep dyspareunia and infertility showed high levels of TNF-alpha and IL-2, respectively. These cytokines are related to the Th1 immune response, and almost 70% of the patients that presented these results had severe endometriosis. The authors concluded that, when specific clinical data are associated with a high production of certain cytokines, there is a Th1 response pattern that may be related to severe endometriosis. The induction of the Th1 immune response was also reported by Fairbanks et al., who demonstrated high levels of IL-12 in patients with severe endometriosis17. The contribution of environmental factors to the development of endometriosis was reviewed by Bellelis et al., who related the influence of these factors, together with the diet, on the genesis of this disease. The authors concluded that the mechanism by which dioxin and dioxin-like compounds (2,3,7,8-tetrachlorodibenzo-p-dioxin[TCDD] and polychlorinated biphenyls [PCBs]) act and change the endometrial physiology is uncertain and speculative. They also affirm that there is insufficient evidence as to the use of specific diets as preventive or even adjuvant factors in the treatment of endometriosis. The genetic and hereditary basis for endometriosis was evidenced in the study by Bellelis et al., in which approximately 5.3% of the patients reported first-degree family history of endometriosis. Familial aggregation, a high concordance rate among monozygotic twins, and a risk of 4% to 7% for first-degree relatives support the contribution of genetic factors to the pathogenesis of this disease14. In this context, the identification of genetic variants or single nucleotide polymorphisms (SNPs) responsible for susceptibility to endometriosis has been researched in recent years19-21. Different classifications have been proposed for the genes responsible for susceptibility to endometriosis (Box 1).
Rev Assoc Med Bras 2012; 58(5):620-632

621

Alessandra Bernadete Trov de Marqui

Box 1 Classification of endometriosis susceptibility genes according to (a) Falconer et al.19 and (b) Tempfer et al.21 a) Group of genes and frequency of positive correlation with endometriosis 1) Cytokines/inflammation, 42.9% 2) Steroid-synthesizing enzymes and detoxification enzymes and receptors, 46.2% 3) Hormone receptors, 60% 4) Estradiol metabolism, *NI 5) Other enzymes and metabolic systems, 42.9% 6) Growth factor systems, 66.7% 7) Adhesion molecules and enzymes from the matrix, 40% 8) Apoptosis, cell-cycle regulation and oncogenes, 22.2% 9) Human leukocyte antigen system and immune components, NI*
*NI, not informed

b) Group of genes 1) Inflammatory mediators 2) Involved in sexual hormone activity 3) Metabolic enzymes 4) Regulators of vascular function and tissue remodeling 5) Other genes linked to endometriosis

This bibliographic review presents a detailed description of the contribution of genetic polymorphisms in genes regulating vascular function and tissue remodeling into the pathogenesis of endometriosis. Genes belonging to this category include: alpha 2-HS glycoprotein (AHSG), epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF), endostatin, plasminogen activator inhibitor 1 (PAI-1), angiotensin I-converting enzyme (ACE), and matrix metalloproteinases (MMPs). For this purpose, a bibliographic research was performed in PubMed, with no time limitation, using the following terms (n = number of articles retrieved): 1 endometriosis and AHSG polymorphisms (n = 1); 2 endometriosis and EGFR polymorphisms (n = 2); 3 endometriosis and VEGF polymorphisms (n = 19, 14 articles were selected for reading); 4 endometriosis and endostatin polymorphisms (n = 1); 5 endometriosis and PAI-1 polymorphisms (n = 6, 4 articles were selected for reading); 6 endometriosis and ACE polymorphisms (n=4); 7 endometriosis and MMPs polymorphisms (n = 11, 9 articles were selected for reading). Articles were selected based on titles and summaries, and the full texts or summaries of those related to the topic were analyzed. An aggregate of 35 publications on polymorphisms in these genes were included in this review. Table 1 summarizes the main results of these studies. Excluded articles associated polymorphisms in these genes to other types of disease/sample (adenomyosis, pterygium, and placenta, n = 4), or endometriosis to polymorphism in another gene (IL-10, n=1), or were included in the review category (n=3), or were published in Chinese and the abstract was not available (n=1).
622
Rev Assoc Med Bras 2012; 58(5):620-632

Articles addressing general information on endometriosis or mentioned in the references of the studies retrieved from PubMed were also researched due to their relevance to this review.

AHSG

and endometriosis

The alpha-2 Heremans Schmid glycoprotein (AHSG) is a protein present in human plasma secreted by the liver. The AHSG gene appears in the endometrium of women with endometriosis, and these women showed high levels of AHSG in serum and peritoneal fluid, in addition to anti-AHSG antibodies22-24. The AHSG gene is located at 3q27-2925 and consists of seven exons and six introns26. Two polymorphisms, termed AHSG1 and AHSG2, have been described and occur in exons 6 and 7, respectively. Allele 1 is characterized by a replacement of cytokine for thymine, i.e., the triplet ACG (threonine) at position 230 was modified to ATG (methionine), resulting in the missense mutation p.T230M (rs4917). Allele 2 corresponds to a change from cytokine to guanine, with the respective missense mutation at position 238 of the protein, from threonine (ACC) to serine (AGC), i.e., p.T238S (rs4918)27. Considering the possibility of associating these SNPs to endometriosis, Kim et al.28 investigated these polymorphisms in 79 Korean women with endometriosis and 105 women without the disease. They observed that those not carrying the AHSG2 allele had twice the risk of developing endometriosis than those with at least one copy of this allele, thus evidencing a positive association between endometriosis and polymorphisms in the AHSG gene in this population.

Genetic polymorphisms

and endometriosis: contribution of genes that regulate vascular function and tissue remodeling

Table 1 Summary of the articles that assessed polymorphisms in genes that regulate vascular function and tissue remodeling in endometriosis. In the sample size, women with endometriosis belonging to the study group followed the stage classification of the American Society for Reproductive Medicine ASRM, 19968
Gene AHSG Exchange of nucleotide/ haplotypes p.T230M (allele 1) p.T238S (allele 2) Sample size 79 women with endometriosis (I=14, II=32, III=8, IV=25) 105 women without endometriosis 122 women with endometriosis 159 women with leiomyoma 139 control women 146 women with endometriosis 181 controls Origin Korea Main findings Reference

Women who did not carry the AHSG2 allele had Kim et al. 200428 twice the risk for endometriosis than those carrying at least one copy of this allele.

EGFR

+ 2073 A/T

Taiwan/China

Association with increased risk for endometriosis and leiomyoma: genotypes and alleles related to EGFR + 2073T These SNPs were not associated with endometriosis

Hsieh et al. 200534

EGFR EGF

+ 2073 A/T + 61 G/A

Japan

Inagaki et al. 200735

VEGF

- 460 C>T

122 women with endometriosis Taiwan/ China 131 women without the disease

Association with increased risk for endometriosis: VEGF -460TT genotype and VEGF -460T allele

Hsieh et al. 200445

VEGF

- 460 C>T + 936 C>T - 2578 A>C - 1154 G>A -460T/-1154G/-2578C -460C/-1154A/-2578A -460C/-1154A/-2578C -460C/-1154G/-2578A -460C/-1154G/-2578C -460T/-1154A/-2578A -460T/-1154A/-2578C -460T/-1154G/-2578A

344 women with endometriosis Northern China No association with endometriosis: VEGF -460 Liu et al. 200946 (III/IV) C>T and VEGF + 936 C>T SNPs 360 women without the disease Association with reduced risk for endometriosis: VEGF -2578AA and VEGF -1154AA genotypes (VEGF -1154A and -2578A alleles protective against the development of endometriosis) Haplotypes that reduced the risk for endometriosis: -460C/-1154A/-2578A -460T/-1154A/-2578A -460T/-1154A/-2578C Haplotypes that increased the risk for endometriosis: -460C/-1154A/-2578C

VEGF

- 460 C>T - 1154 G>A

344 women with endometriosis Northern China (III/IV) 360 controls with endometriosis 174 women with adenomyosis 199 controls with adenomyosis

No association with endometriosis and adenomyosis: VEGF -460 C>T SNP Association with increased risk for endometriosis and adenomyosis: VEGF -1154GG genotype

Liu et al. 200947

VEGF

- 460 C>T + 405 G>C -460C/+405G -460C/+405C -460T/+405G -460T/+405C

215 women with advanced stage endometriosis (III=65 and IV=150) 219 control women 70 fertile women

Korea

No association with endometriosis: VEGF -460C>T SNP and -460/+405 haplotypes Association with increased risk for endometriosis: VEGF + 405CC genotype

Kim et al. 200548

VEGF endostatin

+ 936 C>T 4349 G>A

105 women with endometriosis (I=20, II=41, III=11, IV=33) 101 control women

Korea

Tested polymorphisms were not associated with endometriosis

Kim et al. 200849

(cont.) 623

Rev Assoc Med Bras 2012; 58(5):620-632

Alessandra Bernadete Trov de Marqui

Table 1 Summary of the articles that assessed polymorphisms in genes that regulate vascular function and tissue remodeling in endometriosis. In the sample size, women with endometriosis belonging to the study group followed the stage classification of the American Society for Reproductive Medicine ASRM, 19968 (cont.)
Gene VEGF Exchange of nucleotide/ haplotypes - 460 C>T + 405 G>C -460C/+405G -460C/+405C -460T/+405G -460T/+405C Sample size Origin Main findings Reference Bhanoori et al. 200550

215 women with endometriosis Southern India No association with endometriosis: VEGF and (III=80 and IV=135) -460C>T SNP 210 women without the disease VEGF +405GG genotype was more frequent in patients with endometrioma >3 cm, compared to controls. The frequency of -460T/+405C haplotype was significantly lower in women with endometriosis, compared to controls. 147 cases of endometriosis (I=9, II=15, III=27, and IV=96) 181 controls Japan

VEGF

- 460 C>T + 405 G>C + 936 C>T -460C/+405G -460C/+405C -460T/+405G -460T/+405C

No association with endometriosis: VEGF Ikuhashi et al. 200751 -460C>T SNP, VEGF + 405G>C SNP and -460/+405 haplotypes Association with increased risk for stage III-IV endometriosis: VEGF +936T allele

VEGF

+ 405 G>C

203 women with endometriosis Italy (I/II=78, III/IV=125) 140 women without the disease 186 women with endometriosis (I/II=19, III/IV=167) 180 controls Spain

Association with increased risk for endometriosis: VEGF + 405C allele

Gentilini et al. 200852

VEGF

- 460 C>T + 405 G>C + 936 C>T -460C/+405G -460C/+405C -460T/+405G -460T/+405C

No association with endometriosis: VEGF -460C>T SNP, VEGF + 405G>C SNP and -460/+405 haplotypes Association with increased risk for endometriosis: VEGF + 936T allele

Cosin et al. 200953

VEGF

- 460 C>T + 405 G>C

98 women with endometriosis (I=4, II=18, III=41, IV=35) 94 women without the disease

Turkey

No association with endometriosis: VEGF 460 C>T SNP Association with increased risk for endometriosis: VEGF + 405GC genotype and VEGF +405G allele

Altinkaya et al. 200954

VEGF

- 460 C>T + 405 G>C -460C/+405G -460C/+405C -460T/+405G -460T/+405C

52 women with endometriosis (I/II=11 and III/IV=41) 60 women without endometriosis

Turkey

No association with endometriosis: VEGF -460 Attar et al. 201055 C>T SNPs Association with increased risk for endometriosis: VEGF + 405CC genotype (2.3 times higher risk for the development of endometriosis) and -460T/+405C haplotype Protective factor against endometriosis: VEGF +405G allele (higher frequency in the control group) The analysis by individual SNP or haplotype demonstrated no association with endometriosis Zhao et al. 200856

VEGF

- 460 C>T + 405 G>C + 936 C>T - 2578 A>C -2578A/-460C/+405G -2578C/-460T/+405C -2578C/-460T/+405G

958 family cases of endometriosis (I/II=559, III/ IV=394) 959 controls

Australia

(cont.) 624

Rev Assoc Med Bras 2012; 58(5):620-632

Genetic polymorphisms

and endometriosis: contribution of genes that regulate vascular function and tissue remodeling

Table 1 Summary of the articles that assessed polymorphisms in genes that regulate vascular function and tissue remodeling in endometriosis. In the sample size, women with endometriosis belonging to the study group followed the stage classification of the American Society for Reproductive Medicine ASRM, 19968 (cont.)
Gene VEGF Exchange of nucleotide/ haplotypes + 405 G>C + 936 C>T - 2578 A>C - 1154 G>A -2578A/-1154G/+405G -2578A/-1154A/+405C -2578C/-1154G/+405G -2578C/-1154A/+405C ACE -240 A>T 2350 A>G -240A/2350A -240A/2350G -240T/2350A -240T/2350G VEGF - 460 C>T + 405 G>C 480 women with endometriosis 600 controls Northern Iran Association with increased risk for endometriosis: VEGF + 405CC genotype and VEGF +405C allele. VEGF -460C/T SNP was not associated with the disease. 4G/4G genotype was observed in 52 (69%) of the 75 women with endometriosis and in only five (12%) of the 43 women without the disease. Thus, the 4G allele was associated with endometriosis. 5G/5G genotype was found in two (3%) of the 75 women with endometriosis, compared to 24 (56%) of the 43 controls. Association with endometriosis: PAI-1 4G/4G, 4G/5G genotype and PAI-1 4G allele This polymorphism was not associated with endometriosis Emamifar et al. 201158 Sample size 150 women with endometriosis (I=53, II=39, III=36, IV=22) 199 control women Origin Estonia Main findings Association with reduced risk for endometriosis: VEGF -2578CC genotype. Other SNPs and haplotypes of the VEGF and ACE genes were not associated with the disease. Reference Lamp et al. 201057

PAI-1

4G/5G

75 women with endometriosis 43 control women

Canada

Bedaiwy et al. 200667

PAI-1

4G/5G

170 women with endometriosis (I/II=17, III/IV=153) 219 control women

Spain

Ramon et al. 200868

PAI-1

4G/5G

204 women with endometriosis Italy (I=34, II=25, III=66, IV=79) 164 gynecological control group 329 general population control group 140 women with endometriosis (I/II=79, III/IV=61) 148 controls 150 women with endometriosis (III/IV) 159 women without endometriosis Brazil

This polymorphism was not associated with endometriosis

Gentilini et al. 200969

PAI-1

4G/5G

This SNP was associated with increased risk for endometriosis related to infertility

Gonalves-Filho et al. 201170

ACE

2350 A>G -240 A>T

Taiwan/China

Association with increased risk for endometriosis: genotypes and alleles related to ACE 2350G and ACE -240T

Hsieh et al. 200573

(cont.) 625

Rev Assoc Med Bras 2012; 58(5):620-632

Alessandra Bernadete Trov de Marqui

Table 1 Summary of the articles that assessed polymorphisms in genes that regulate vascular function and tissue remodeling in endometriosis. In the sample size, women with endometriosis belonging to the study group followed the stage classification of the American Society for Reproductive Medicine ASRM, 19968 (cont.)
Gene ACE Exchange of nucleotide/ haplotypes I/D Sample size 125 women with endometriosis (III/IV) 120 women with leiomyoma 128 women without both pathologies Origin Taiwan/ China Main findings Reference

Association with increased risk for Hsieh et al. 200774 endometriosis: genotypes and alleles related to ACE I Association with moderate risk for leiomyoma: genotypes and alleles related to ACE I

ACE

I/D

121 women with endometriosis 122 women without endometriosis 100 women with endometriosis 150 control women 80 patients with adenomyosis

Poland

This polymorphism was not associated with endometriosis

Kowalczynska et al. 201175

MMP-1 MMP-3

1G/2G 5A/6A 1G/5A 1G/6A 2G/5A 2G/6A

China

Association with increased risk for endometriosis: MMP-1 2G/2G and 1G/2G genotype MMP-1 2G allele and 2G/6A haplotype Association with increased risk for adenomyosis: MMP-1 2G/2G genotype and MMP-1 2G allele No association with endometriosis and adenomyosis: MMP-3 5A/6A SNP

Kang et al. 200588

MMP-1 MMP-3

1G/2G 5A/6A 1G/6A 1G/5A 2G/6A 2G/5A

100 women with endometriosis (III/IV) 150 control women

Northern China Association with increased risk for endometriosis: MMP1 2G/2G, 1G/2G genotype, MMP1 2G allele and 2G/6A haplotype No association with endometriosis: MMP3 5A/6A SNP

Shan et al. 200589

MMP-1 MMP-3

1G/2G 5A/6A

56 women with endometriosis 71 control group

Italy

Polymorphisms in this gene were not associated with endometriosis.

Ferrari et al. 200690

MMP-1 MMP-2 MMP-3 MMP-7 MMP-12 MMP-13 MMP-2

1G/2G -1575 G>A (MMP2.1) -1306 C>T (MMP2.2) 5A/6A -153C/T (MMP 7.1) -181 A/G (MMP 7.2) -82 A/G -77 A/G -1306 C>T -735 C>T -1306C/-735C -1306C/-735T -1306T/-735C -1306T/-735T

227 women with endometriosis Paris/France (ovarian endometriosis or endometrioma=64, superficial endometriosis=24 and deep endometriosis=139) 241 controls

The MMP12-MMP13 A/G-A/A combined genotype was associated with superficial endometriosis

Bhorghese et al. 200891

298 women with endometriosis China 324 controls 180 patients with adenomyosis

TIMP-2

-418 G>C

Association with increased risk for adenomyosis: MMP-2 -1306CC genotype Association with reduced risk for endometriosis: TIMP-2 -418CC genotype (frequency of this genotype was lower in patients with endometriosis than in control women) No association with endometriosis: MMP-2 -1306 C>T SNP No association with endometriosis: TIMP-2 -418G>C SNP No association with endometriosis: and adenomyosis: MMP-2 -1306/-735 haplotypes and MMP-2 -735 C>T SNP

Zhao et al. 200892

(cont.) 626
Rev Assoc Med Bras 2012; 58(5):620-632

Genetic polymorphisms

and endometriosis: contribution of genes that regulate vascular function and tissue remodeling

Table 1 Summary of the articles that assessed polymorphisms in genes that regulate vascular function and tissue remodeling in endometriosis. In the sample size, women with endometriosis belonging to the study group followed the stage classification of the American Society for Reproductive Medicine ASRM, 19968 (cont.)
Gene MMP-2 Exchange of nucleotide/ haplotypes -1306 C/T -735 C/T -1306C/-735C -1306C/-735T -1306T/-735C -1306T/-735T TIMP-2 MMP-2 -418 G/C -735 C/T -790T/G -1575 G/A -735C/-790T/-1575G -735C/-790G/-1575A -735T/-790T/-1575G -735T/-790G/-1575A -735C/-790T/-1575A -735C/-790G/-1575G -735T/-790T/-1575A -735T/-790G/-1575G MMP-9 MMP-7 MMP-9 -1562 C/T -181 A/G -1562 C/T 143 women with endometriosis (III/IV) 160 control women 76 women with adenomyosis Northern China Association with endometriosis and adenomyosis: MMP-7 -181G allele SNP of the MMP-9 gene was not associated with the occurrence of endometriosis and adenomyosis. Korea The risk of developing endometriosis was not associated with the individually studied SNP. The haplotype analysis showed significant association with the disease. Association with endometriosis of AC (279Q/P574), GG (R279/ 574R) and CA (-1562C/668Q) haplotypes Shan et al. 200695 150 women with endometriosis (I/II=92, III/IV=58) 199 healthy women Estonia Association with increased risk for endometriosis: MMP-2 -735CC genotype (stage I/II endometriosis) MMP-9 -1562 TT or TC genotype (stage III/IV endometriosis). The eight tested haplotypes were not associated with endometriosis. MMP-2 -790T/G and -1575G/A SNPs were not associated with the disease. Saare et al. 201094 Sample size 298 women with endometriosis (III/IV) 324 controls Origin North China Main findings Association with reduced risk for endometriosis: TIMP-2 -418CC genotype No association with endometriosis: -1306C/T, -735C/T SNPs and -1306/-735 haplotypes Reference Kang et al. 200893

MMP-9

-1562 C>T R279Q (2678G>A) P574R (4859C>G) R668Q (5546G>A) 2678G/4859C 2678A/4859G 2678G/4859G 2678A/4859C -1562C/5546G -1562C/5546A -1562T/5546G -1562T/5546A

225 women with endometriosis (III/IV) 198 control women

Han et al. 200996

EGFR, VEGF,

endostatin and endometriosis

Endometriosis shows characteristics similar to neoplasias, such as invasiveness and neovascularization, the latter considered an important phenomenon for the implantation of endometrial cells in ectopic sites. Thus, growth and other angiogenic factors, such as the VEGF and EGFR, could be related to the development of endometriosis29-32. EGFR is a transmembrane glycoprotein that plays important roles in controlling cell growth, differentiation,

and motility. The EGFR gene is located at 7p12 and a polymorphism characterized by exchange of base A for T at position 2073 of exon 21 has been observed33. This modification changes the stop codon (TGA) by synthesis of the amino acid cysteine (TGT). Aiming at assessing whether the EGFR +2073A/T SNP could be used as a susceptibility flag for endometriosis, Hsieh et al. assessed 122 Taiwanese women with this pathology and 139 controls, and associated the TT and AT genotypes and the T allele to high risk
Rev Assoc Med Bras 2012; 58(5):620-632

627

Alessandra Bernadete Trov de Marqui

for the disease34. However, subsequent studies did not associate this SNP to endometriosis in Japanese people35. VEGF induces endothelial cell proliferation, migration, differentiation, and formation of capillaries, which contribute to the pathogenesis and progression of endometriosis. Additionally, studies have shown high levels of VEGF in the peritoneal fluid, serum, mRNA expression, and proteins of patients with endometriosis36-42. These data reinforce the role of VEGF in the pathogenesis of endometriosis. The VEGF gene is located at 6p21.343, consists of eight exons, and shows alternative splicing, which is responsible for forming several proteins. At least 30 SNPs were described in this gene44. In order to determine a genetic predisposition to endometriosis, some studies were developed to investigate polymorphisms of the VEGF gene in women with endometriosis. These studies were conducted in China45-47, Korea48,49, India50, Japan51, Italy52, Spain53, Turkey54,55, Australia56, Estonia57, and Iran58. Assessed SNPs were 460 C/T (rs833061), +405 G/C (also known as -634 G/C, rs2010963), +936 C/T (rs3025039), -1154 G/A (rs1570360), and -2578 A/C (rs699947). 460 C/T polymorphism was researched in several studies45-48,50,51,53-56,58. Only the study of Hsieh et al.45 associated the TT genotype and T allele to high risk for endometriosis. With respect to +405 G/C polymorphism, no association between this SNP and endometriosis was reported by Ikuhashi et al.51, Zhao et al.56, Cosin et al.53, and Lamp et al.57, but a significant association was reported in six other studies48,50,52,54,55,58. However, these studies showed conflicting results regarding the relation between genotypes and alleles and endometriosis. Considering genotype and allele, Kim et al.48, Gentilini et al.52, Attar et al.55, and Emamifar et al.58 associated +405 CC and therefore the C allele, to endometriosis; Bhanoori et al.50 and Altinkaya et al.54 related the +405 GG and +405 GC genotypes to the disease, respectively. Thus, some works associated the C allele with endometriosis48,52,55,58, while other works associated the G allele50,54 with the disease. A positive association between endometriosis and SNP at position 405 became evident, suggesting an effective contribution of such polymorphism to the pathogenesis of endometriosis. The discrepancy regarding the results of analysis of +405 G/C VEGF SNP among the published works could be explained by the different populations studied, whose ethnic differences would explain the causes of these conflicting findings. The studies by Ikushashi et al.51 and Cosin et al.53 investigated the same polymorphisms (-460 C/T, +405 G/C and +936 C/T) in populations with different ethnic origins. Both reported a positive association with respect to VEGF 936 T allele in women with endometriosis, while other authors46,49,56,57 did not confirm this association.
628
Rev Assoc Med Bras 2012; 58(5):620-632

-1154 G/A polymorphism was assessed by Liu et al.46,47 and by Lamp et al.57. Studies by the same group of researchers46,47 showed different results, as the AA genotype was associated with reduced risk for endometriosis46, and the GG genotype was associated with high risk for the disease47. Different alleles of the -2578 C/A SNP were associated with reduced risk for endometriosis. The A allele of this polymorphism was reported to be protective in relation to the development of endometriosis46; Lamp et al.57 associated this protection with the C allele. This polymorphism was not associated with endometriosis in a study by Zhao et al.56. The study by Zhao et al.56 that assessed VEGF -460 C/T, +405 G/C, -2578 A/C, and +936 C/T SNPs (the latter also investigated by Kim et al.49), was the only study that did not associate these SNPs with endometriosis. Despite the conflicting results regarding some SNPs, at least one polymorphism was associated with endometriosis in the abovementioned works. The 4349 G/A polymorphism of the endostatin gene was assessed by Kim et al.49. Endostatin is a specific endogenous anti-angiogenic factor derived from the proteolysis of type XVIII collagen, and it induces inhibition of endothelial cell proliferation, migration, and apoptosis. Studies have demonstrated the role of endostatin in endometriotic lesions in animal models59,60. This SNP was not related to endometriosis, but the endostatin level in serum was negatively correlated with the development of this disease49. In addition to the individual analysis of the VEGF gene per SNP, some studies carried out the research per haplotypes. The -460/+405 haplotype was not associated with endometriosis in the studies by Kim et al.48, Ikushashi et al.51, and Cosin et al.53. The -460T/+405C haplotype showed lower frequency in women with endometriosis50; in another study, it was associated with high risk for this disease55. Other haplotypes not related to endometriosis were -2578/-460/+40556 and -2578/-1154/+40557. -460C/1154A/-2578A, -460T/-1154A/-2578A, and -460T/1154A/-2578C haplotypes were associated with reduced risk for endometriosis, while -460C/-1154A/-2578C was associated with high risk for the disease46. Therefore, only eight out of 14 studies that assessed the VEGF gene performed analyses per haplotype, with result of positive association with endometriosis in only three studies.

PAI-1

and endometriosis

The plasminogen activation system includes plasminogen activators and their inhibitors, which are involved in tissue degradation and remodeling under normal and pathological conditions. Two plasminogen activator inhibitors (PAIs), termed PAI-1 and PAI-2, regulate the plasminogen activation system61,62. The main PAI is PAI-1, also known as endothelial cell PAI, which also plays an important role in signal transduction, cell adherence, and cell migration63.

Genetic polymorphisms

and endometriosis: contribution of genes that regulate vascular function and tissue remodeling

The PAI-1 gene, whose official symbol is SERPINE1, is located at 7q21.3-q22 and contains 9 exons. A guanine (G) insertion/deletion polymorphism in the promoter region of the PAI-1 gene at position -675, termed 4G/5G, has been described and is involved in regulating the synthesis of this inhibitor. In vitro studies have showed that the 4G allele is associated with increased gene expression from its binding to an activator protein, while the 5G allele contains an additional binding site for the DNA-binding protein acting as a transcriptional repressor64-66. Four studies were performed in women with endometriosis from Canada67, Spain68, Italy69, and Brazil70. A positive association for PAI-1 4G/5G SNP was reported by Bedaiwy et al.67 and Gonalves-Filho et al.70. According to Bedaiwy et al., patients with 4G/5G and 4G/4G genotypes are 38 and 441 times more likely to have endometriosis than those with a 5G/5G genotype, respectively67. In this study, 118 women were assessed (75 with endometriosis and 43 controls) and the 4G allele frequency was significantly higher in those with endometriosis. Nonetheless, these findings were not replicated in two studies involving a large number of patients and controls, one with 389 women (170 with endometriosis and 219 controls)68, and the other with 204 women with endometriosis and 164 controls69. Therefore, according to studies of Ramon et al.68 and Gentilini et al.69, the predisposition to endometriosis did not involve the 4G/5G PAI-1 polymorphism.

T allele) were associated with high susceptibility to endometriosis in this population. However, in 2010, Lamp et al. did not identify an association between these two SNPs and endometriosis in 150 women with endometriosis and 199 controls from Estonia57. These same researchers investigated -240/2350 haplotypes and did not associate them with endometriosis. Regarding polymorphism in the ACE I/D gene, the genotypes and alleles related to the ACE I were strongly associated with endometriosis in 125 patients with endometriosis and 128 controls74. However, Kowalczynska et al.75 investigated this same SNP in 121 women with endometriosis and 122 without endometriosis, and did not associate it to the disease. Therefore, only studies in Taiwanese/Chinese subjects73,74 have demonstrated positive associations of the ACE polymorphism at position 2350, 240, and ACE I/D with endometriosis. When such polymorphisms are assessed in people of other ethnic origins, the results of positive association were not confirmed57,75.

MMPs

and endometriosis

ACE

and endometriosis

The ACE catalyzes the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor. Thus, ACE activity is associated with angiogenesis, which plays a key role in the pathogenesis of endometriosis. The presence of angiotensin receptors in the endometrial tissue has been demonstrated. Angiotensin II in endometrial stromal cells was mediated via angiotensin I receptors71, and could increase the intracellular calcium concentration by interaction with the angiotensin receptor in endometrial stromal cells72. These findings suggest a contribution of ACE to the development of endometriosis and the endometrium. The ACE gene is located at 17q23.3 and three SNPs were assessed to verify association with endometriosis: -240 A/T (promoter region rs4291), 2350 A/G (alteration in exon 17, Thr776Thr rs4343), and one insertion/ deletion (I/D) of one Alu sequence (287 pb) in intron 16. Hsieh et al.73 and Lamp et al.57 investigated polymorphisms at position 240 and 2350 and found conflicting results. In 2005, Hsieh et al. assessed 150 women with endometriosis and 159 controls from Taiwan/China73. They observed that genotypes and alleles related to ACE 2350G (heterozygous AG, homozygous GG, and G allele) and ACE-240T (heterozygous AT, homozygous TT, and

MMPs belong to a large group of 23 proteases that regulate tissue remodeling by degrading the structural components of the extracellular matrix (ECM). MMPs also control basic cellular functions (proliferation, differentiation, motility, apoptosis), as they regulate the ECM proteins that interact with cells76. High levels of MMPs were found in ectopic endometrium when compared to eutopic endometrium in women with endometriosis. Therefore, the overexpression of MMPs may contribute to the development of endometriosis77-84. Genetic polymorphisms located in the promoter region of the MMPs genes could increase the levels of gene expression, and may be associated with genetic predisposition to various diseases85-87. Thus, polymorphisms in the MMP-188-91, MMP91-94 2 , MMP-388-91, MMP-791,95, MMP-994-96, MMP-1291, MMP-1391, and TIMP-292,93 genes were investigated to verify whether they contribute to the development of endometriosis. An I/D of guanine in the promoter region of the MMP1 (-1607 1G/2G) (rs112925) gene was associated with increased risk for endometriosis in Chinese women according to Kang et al.88 and Shan et al.89. Both studies showed a role of the 2G allele in the pathogenesis of endometriosis in 100 women with endometriosis and 150 controls. Polymorphisms in this gene were not associated with endometriosis in Italian90 and French91 women. Four SNPs in the promoter of the MMP-2 gene have been described: -735 C/T (rs2285053), -790 T/G (rs243864), -1306 C/T (rs243865), and -1575 G/A
Rev Assoc Med Bras 2012; 58(5):620-632

629

Alessandra Bernadete Trov de Marqui

(rs243866). -735 C/T polymorphism was investigated by Zhao et al.92, Kang et al.93, and Saare et al.94. Only in the study of Saare et al. was the -735CC genotype associated with increased risk for stage I-II endometriosis94. The -790 T/G SNP investigated by Saare et al.94; the -1306 C/T investigated by Zhao et al.92, Kang et al.93, and Bhorghese et al.91; and the -1575 G/A analyzed by Bhorghese et al.91 and Saare et al.94 showed no significant association with endometriosis. No association with endometriosis was reported for the -1612 5A/6A and -1171 5A/6A SNPs of the MMP-3 gene88-91. 1G/6A, 1G/5A, 2G/6A, and 2G/5A haplotypes related to the MMP-1 and MMP-3 genes were investigated by Kang et al.88 and Shan et al.89. In both studies, the 2G/6A haplotype was associated with increased risk for endometriosis. For the -1306/-735 and -735/-790/-1575 haplotypes of the MMP-2 gene, no association with endometriosis was reported by Zhao et al92, Kang et al.93, and Saare et al.94. Two polymorphisms in the promoter region of the MMP-7 gene (-153 C/T and -181 A/G) were investigated for association with endometriosis91,95. Only the G allele of -the 181 A/G (rs1799750) SNP was associated with increased risk for endometriosis and adenomyosis in Chinese women95. R279Q (2678G>A), P574R (4859C>G), R668Q (5546G>A), and -1562 C>T (rs3918242) polymorphisms of the MMP-9 gene were investigated by Han et al.96 and, in the analysis of individual SNP, showed no association with endometriosis. However, the AC (279Q/P574), GG (R279/574R) and CA (-1562C/668Q) haplotypes were significantly associated with endometriosis. In his research, Han et al.96 concluded that haplotype analysis of the MMP9 gene was more informative than individual polymorphism analysis. Regarding the -1562 C> T SNP that had been previously investigated by Shan et al.95, the result was consistent with the study of Han et al.82. However, a study by Saare et al.94 showed that the -1562 TT and TC genotypes of the MMP-9 gene were associated with advanced stage endometriosis (III-IV). The MMP-12 MMP-13 A/GA/A combined genotype of MMP-12 and MMP-13 genes contributed to the development of superficial endometriosis in French women91. Regarding the -418 G/C SNP of the TIMP-2 gene, the -418CC genotype was associated with reduced risk for endometriosis in the two studies92,93, and the C allele was a protective factor against the development of endometriosis in Chinese women. Regarding haplotype analysis, of nine studies on MMP genes, six assessed haplotypes, and a positive association between endometriosis and the haplotypes of MMP-1, 3, and 988,89,96 genes was reported, as well as a negative association for haplotypes of the MMP-292-94 gene.
630
Rev Assoc Med Bras 2012; 58(5):620-632

Final

considerations

In this review, a detailed description of the contribution of genetic polymorphisms in genes that regulate vascular function and tissue remodeling into the pathogenesis of endometriosis has been presented. Some polymorphisms of the VEGF (-460 C/T, +405 G/C, +936 C/T), PAI, MMP1, 2, and 3 genes have been widely studied, while others of the AHSG, EGF, endostatin, and VEGF (-1154 G/A, -2578 A/C) genes were not. In the latter case, additional studies are required to confirm the findings by the few studies that have analyzed these SNPs. Additionally, studies that found a positive or negative association of SNP with endometriosis emphasize the relevance of studies with a large number of control cases to confirm their findings. Haplotype analysis was carried out only for the VEGF (-460, +405, -1154 and -2578), ACE (-240/2350) and MMP-1, 2, 3 and 9 genes, and in most studies, there was no association with endometriosis. Of the eight studies that analyzed haplotypes of the VEGF gene, five did not associate them with endometriosis. Haplotypes of ACE and MMP-2 genes were not associated with endometriosis, while those of MMP-1, 3, and 9 genes were related to a high risk for the disease. It is worth highlighting that studies involving polymorphisms are complex, since a genetic association, although valid for a specific ethnic population, may not be relevant to individuals of another ethnicity.

References
1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. Giudice LC, Kao LC. Endometriosis. Lancet. 2004;364(9447):1789-99. Bulun SE. Endometriosis. N Engl J Med. 2009;360(3):268-79. Bellelis P, Dias JA Jr, Podgaec S, Gonzales M, Baracat EC, Abro MS. Epidemiological and clinical aspects of pelvic endometriosisa case series. Rev Assoc Med Bras. 2010;56(4):467-71. Petta CA, Matos AM, Bahamondes L, Fandes D. Current practice in the management of symptoms of endometriosis: a survey of Brazilian gynecologists. Rev Assoc Med Bras. 2007;53(6):525-9. Baldi A, Campioni M, Signorile PG. Endometriosis: pathogenesis, diagnosis, therapy and association with cancer (review). Oncol Rep. 2008;19(4):843-6. Bassi MA, Podgaec S, Dias Jnior JA, Sobrado CW, D Amico Filho N, Abro MS. Bowel endometriosis: a benign disease?. Rev Assoc Med Bras. 2009;55(5):611-6. Ncul AP, Spritzer PM. Current aspects on diagnosis and treatment of endometriosis. Rev Bras Ginecol Obstet. 2010;32(6):298-307. Revised American Society for Reproductive Medicine classification of endometriosis: 1996. Fertil Steril. 1997;67(5):817-21. Mathur SP. Autoimmunity in endometriosis: relevance to infertility. Am J Reprod Immunol. 2000;44(2):89-95. Berkkanoglu M, Arici A. Immunology and endometriosis. Am J Reprod Immunol. 2003;50(1):48-59. Bellelis P, Podgaec S, Abro MS. Environmental factors and endometriosis. Rev Assoc Med Bras. 2011;57(4):448-52. Zondervan KT, Cardon LR, Kennedy SH. The genetic basis of endometriosis. Curr Opin Obstet Gynecol. 2001;13(3):309-14. Bischoff F, Simpson JL. Genetic basis of endometriosis. Ann N Y Acad Sci. 2004;1034:284-99. Simpson JL, Bischoff FZ, Kamat A, Buster JE, Carson SA. Genetics of endometriosis. Obstet Gynecol Clin North Am. 2003;30(1):21-40. Harada T, Iwabe T, Terakawa N. Role of cytokines in endometriosis. Fertil Steril. 2001;76(1):1-10. Podgaec S, Abrao MS, Dias Jr JA, Rizzo LV, Oliveira RM, Baracat EC. Endometriosis: an inflammatory disease with a Th2 immune response component. Hum Reprod. 2007;22(5):1373-9. Fairbanks F, Abro MS, Podgaec S, Dias Jr JA, de Oliveira RM, Rizzo LV. Interleukin-12 but not interleukin-18 is associated with severe endometriosis. Fertil Steril. 2009;91(2):320-4.

Genetic polymorphisms

and endometriosis: contribution of genes that regulate vascular function and tissue remodeling

18. Podgaec S, Dias Junior JA, Chapron C, Oliveira RM, Baracat EC, Abro MS. Th1 and Th2 immune responses related to pelvic endometriosis. Rev Assoc Med Bras. 2010;56(1):92-8. 19. Falconer H, DHooghe T, Fried G. Endometriosis and genetic polymorphisms. Obstet Gynecol Surv. 2007;62(9):616-28. 20. Montgomery GW, Nyholt DR, Zhao ZZ, Treloar SA, Painter JN, Missmer SA, et al. The search for genes contributing to endometriosis risk. Hum Reprod Update. 2008;14(5):447-57. 21. Tempfer CB, Simoni M, Destenaves B, Fauser BC. Functional genetic polymorphisms and female reproductive disorders: part II - endometriosis. Hum Reprod Update. 2009;15(1):97-118. 22. Pillai S, Zhou GX, Arnaud P, Jiang H, Butler WJ, Zhang H. Antibodies to endometrial transferrin and alpha 2-Heremans Schmidt (HS) glycoprotein in patients with endometriosis. Am J Reprod Immunol. 1996;35(5):483-94. 23. Mathur SP, Holt VL, Lee JH, Jiang H, Rust PF. Levels of antibodies to transferrin and alpha 2-HS glycoprotein in women with and without endometriosis. Am J Reprod Immunol. 1998;40(2):69-73. 24. Mathur SP, Lee JH, Jiang H, Arnaud P, Rust PF. Levels of transferring and alpha2-HS glycoprotein in women with and without endometriosis. Autoimmunity. 1999;29(2):121-7. 25. Magnuson VL, McCombs JL, Lee CC, Yang F, Bowman BH, McGill JR. Human alpha 2-HS-glycoprotein localized to 3q27q29 by in situ hybridization. Cytogenet Cell Genet.1988;47(1-2):72-4. 26. Osawa M, Umetsu K, Sato M, Ohki T, Yukawa N, Suzuki T et al. Structure of the gene encoding human alpha 2-HS glycoprotein (AHSG). Gene. 1997;196(1-2):121-5. 27. Osawa M, Umetsu K, Ohki T, Nagasawa T, Suzuki T, Takeichi S. Molecular evidence for human alpha 2-HS glycoprotein (AHSG) polymorphism. Hum Genet. 1997;99(1):18-21. 28. Kim JG, Kim H, Ku SY, Kim SH, Choi YM, Moon SY. Association between human alpha 2-Heremans Schmidt glycoprotein (AHSG) polymorphism and endometriosis in Korean women. Fertil Steril. 2004;82(6):1497-500. 29. Deguchi M, Ishiko O, Sumi T, Yoshida H, Yamamoto K, Ogita S. Expression of angiogenic factors in extrapelvic endometriosis. Oncol Rep. 2001;8(6):13179. 30. Taylor RN, Lebovic DI, Mueller MD. Angiogenic factors in endometriosis. Ann NY Acad Sci. 2002;955:89-100; discussion 118, 396-406. 31. May K, Becker CM. Endometriosis and angiogenesis. Minerva Ginecol. 2008;60(3):245-54. 32. Garca Manero M, Olartecoechea B, Aub M, Alczar JL, Lpez G. Angiogenesis and endometriosis. Rev Med Univ Navarra. 2009;53(2):8-13. 33. Shintani S, Matsuo K, Crohin CC, McBride J, Tsuji T, Donoff RB, et al. Intragenic mutation analysis of the human epidermal growth factor receptor (EGFR) gene in malignant human oral keratinocytes. Cancer Res 1999;59(16):4142-7. 34. Hsieh YY, Chang CC, Tsai FJ, Lin CC, Tsai CH. T homozygote and allele of epidermal growth factor receptor 2073 gene polymorphism are associated with higher susceptibility to endometriosis and leiomyomas. Fertil Steril. 2005;83(3):796-9. 35. Inagaki M, Yoshida S, Kennedy S, Takemura N, Deguchi M, Ohara N, et al. Association study between epidermal growth factor receptor and epidermal growth factor polymorphisms and endometriosis in a Japanese population. Gynecol Endocrinol. 2007;23(8):474-8. 36. McLaren J, Prentice A, Charnock-Jones DS, Smith SK. Vascular endothelial growth factor (VEGF) concentrations are elevated in peritoneal fluid of women with endometriosis. Hum Reprod. 1996;11(1):220-3. 37. Donnez J, Smoes P, Gillerot S, Casanas-Roux F, Nisolle M. Vascular endothelial growth factor (VEGF) in endometriosis. Hum Reprod. 1998;13(6):1686-90. 38. Mahnke JL, Dawood MY, Huang JC. Vascular endothelial growth factor and interleukin-6 in peritoneal fluid of women with endometriosis. Fertil Steril. 2000;73(1):166-70. 39. Tan XJ, Lang JH, Liu DY, Shen K, Leng JH, Zhu L. Expression of vascular endothelial growth factor and thrombospondin-1 mRNA in patients with endometriosis. Fertil Steril. 2002;78(1):148-53. 40. Matalliotakis IM, Goumenou AG, Koumantakis GE, Neonaki MA, Koumantakis EE, Dionyssopoulou E, et al. Serum concentrations of growth factors in women with and without endometriosis: the action of anti-endometriosis medicines. Int Immunopharmacol. 2003;3(1):81-9. 41. Gilabert-Estells J, Ramn LA, Espaa F, Gilabert J, Vila V, Rganon E, et al. Expression of angiogenic factors in endometriosis: relationship to fibrinolytic and metalloproteinase systems. Hum Reprod. 2007;22(8):2120-7. 42. Pupo-Nogueira A, de Oliveira RM, Petta CA, Podgaec S, Dias JA Jr, Abrao MS. Vascular endothelial growth factor concentrations in the serum and peritoneal fluid of women with endometriosis. Int J Gynaecol Obstet. 2007;99(1):33-7. 43. Vincenti V, Cassano C, Rocchi M, Persico G. Assignment of the vascular endothelial growth factor gene to human chromosome 6p21.3. Circulation. 1996;93(8):1493-5. 44. Watson CJ, Webb NJ, Bottomley MJ, Brenchley PE. Identification of polymorphisms within the vascular endothelial growth factor (VEGF) gene: correlation with variation in VEGF protein production. Cytokine. 2000;12(8):1232-5. 45. Hsieh YY, Chang CC, Tsai FJ, Yeh LS, Lin CC, Peng CT. T allele for VEGF gene-460 polymorphism at the 5-untranslated region: association with a higher susceptibility to endometriosis. J Reprod Med. 2004;49(6):468-72.

46. Liu Q, Li Y, Zhao J, Sun DL, Duan YN, Wang N, et al. Association of polymorphisms -1154G/A and -2578C/A in the vascular endothelial growth factor gene with decreased risk of endometriosis in Chinese women. Hum Reprod. 2009;24(10):2660-6. 47. Liu Q, Li Y, Zhao J, Zhou RM, Wang N, Sun DL, et al. Association of single nucleotide polymorphisms in VEGF gene with the risk of endometriosis and adenomyosis. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009;26(2):165-9. 48. Kim SH, Choi YM, Choung SH, Jun JK, Kim JG, Moon SY. Vascular endothelial growth factor gene +405 C/G polymorphism is associated with susceptibility to advanced stage endometriosis. Hum Reprod. 2005;20(10):2904-8. 49. Kim JG, Kim JY, Jee BC, Suh CS, Kim SH, Choi YM. Association between endometriosis and polymorphisms in endostatin and vascular endothelial growth factor and their serum levels in Korean women. Fertil Steril. 2008;89(1):243-5. 50. Bhanoori M, Arvind Babu K, Pavankumar Reddy NG, Lakshmi Rao K, Zondervan K, Deenadayal M, et al. The vascular endothelial growth factor (VEGF) +405G>C 5-untranslated region polymorphism and increased risk of endometriosis in South Indian women: a case control study. Hum Reprod. 2005;20(7):1844-9. 51. Ikuhashi Y, Yoshida S, Kennedy S, Zondervan K, Takemura N, Deguchi M, et al. Vascular endothelial growth factor +936 C/T polymorphism is associated with an increased risk of endometriosis in a Japanese population. Acta Obstet Gynecol Scand. 2007;86(11):1352-8. 52. Gentilini D, Somigliana E, Vigano P, Vignali M, Busacca M, Di Blasio AM. The vascular endothelial growth factor +405G>C polymorphism in endometriosis. Hum Reprod. 2008;23(1):211-5. 53. Cosn R, Gilabert-Estells J, Ramn LA, Espaa F, Gilabert J, Romeu A, et al. Vascular endothelial growth factor polymorphisms (-460C/T, +405G/C, and 936C/T) and endometriosis: their influence on vascular endothelial growth factor expression. Fertil Steril. 2009;92(4):1214-20. 54. Altinkaya SO, Ugur M, Ceylaner G, Ozat M, Gungor T, Ceylaner S. Vascular endothelial growth factor +405 C/G polymorphism is highly associated with an increased risk of endometriosis in Turkish women. Arch Gynecol Obstet. 2011 Feb;283(2):267-72. 55. Attar R, Agachan B, Kuran SB, Toptas B, Eraltan IY, Attar E, et al. Genetic variants of vascular endothelial growth factor and risk for the development of endometriosis. In Vivo. 2010;24(3):297-301. 56. Zhao ZZ, Nyholt DR, Thomas S, Treloar SA, Montgomery GW. Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis. Mol Hum Reprod. 2008;14(9):531-8. 57. Lamp M, Saare M, Laisk T, Karro H, Kadastik U, Metspalu A, et al. Genetic variations in vascular endothelial growth factor but not in angiotensin I-converting enzyme genes are associated with endometriosis in Estonian women. Eur J Obstet Gynecol Reprod Biol. 2010;153(1):85-9. 58. Emamifar B, Salehi Z, Mehrafza M, Mashayekhi F. The vascular endothelial growth factor (VEGF) polymorphisms and the risk of endometriosis in northern Iran. Gynecol Endocrinol. 2012;28(6):447-60. 59. Becker CM, Sampson DA, Rupnick MA, Rohan RM, Efstathiou JA, Short SM, et al. Endostatin inhibits the growth of endometriotic lesions but does not affect fertility. Fertil Steril. 2005;84(Suppl 2):1144-55. 60. Becker CM, Sampson DA, Short SM, Javaherian K, Folkman J, DAmato RJ. Short synthetic endostatin peptides inhibit endothelial migration in vitro and endometriosis in a mouse model. Fertil Steril. 2006;85(1):71-7. 61. Lijnen HR. Pathophysiology of the plasminogen/plasmin system. Int J Clin Lab Res 1996;26(1):1-6. 62. Gilabert-Estelles J, Castello R, Gilabert J, Ramon LA, Espana F, Romeu A, et al. Plasminogen activators and plasminogen activator inhibitors in endometriosis. Front Biosci. 2005;10:1162-76. 63. Harbeck N, Krger A, Sinz S, Kates RE, Thomssen C, Schmitt M, et al. Clinical relevance of the plasminogen activator inhibitor type 1--a multifaceted proteolytic factor. Onkologie. 2001;24(3):238-44. 64. Dawson SJ, Wiman B, Hamsten A, Green F, Humphries S, Henney AM. The two allele sequences of a common polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene respond differently to interleukin-1 in HepG2 cells. J Biol Chem. 1993;268(15):10739-45. 65. Eriksson P, Kallin B, Vant Hooft FM, Bavenholm P, Hamsten A. Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA. 1995;92(6):1851-5. 66. Grancha S, Estells A, Tormo G, Falco C, Gilabert J, Espaa F, et al. Plasminogen activator inhibitor-1 (PAI-1) promoter 4G/5G genotype and increased PAI-1 circulating levels in postmenopausal women with coronary artery disease. Thromb Haemost. 1999;81(4):516-21. 67. Bedaiwy MA, Falcone T, Mascha EJ, Casper RF. Genetic polymorphism in the fibrinolytic system and endometriosis. Obstet Gynecol. 2006;108(1):162-8. 68. Ramn LA, Gilabert-Estells J, Cosn R, Gilabert J, Espaa F, Castell R, et al. Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism and endometriosis. Influence of PAI-1 polymorphism on PAI-1 antigen and mRNA expression. Thromb Res. 2008;122(6):854-60. 69. Gentilini D, Vigano P, Castaldi D, Mari D, Busacca M, Vercellini P, et al. Plasminogen activator inhibitor-1 4G/5G polymorphism and susceptibility to endometriosis in the Italian population. Eur J Obstet Gynecol Reprod Biol. 2009;146(2):219-21.

Rev Assoc Med Bras 2012; 58(5):620-632

631

Alessandra Bernadete Trov de Marqui

70. Gonalves-Filho RP, Brandes A, Christofolini DM, Lerner TG, Bianco B, Barbosa CP. Plasminogen activator inhibitor-1 4G/5G polymorphism in infertile women with and without endometriosis. Acta Obstet Gynecol Scand. 2011;90(5):473-7. 71. Braileanu GT, Simasko SM, Speth RC, Daubert D, Hu J, Mirando MA. Angiotensin II increases intracellular calcium concentration in pig endometrial stromal cells through type 1 angiotensin receptors, but does not stimulate phospholipase C activity or prostaglandin F2alpha secretion. Reprod Fertil Dev. 2002;14(3-4):199-205. 72. Braileanu GT, Simasko SM, Hu J, Assiri A, Mirando MA. Effects of arginineand lysine-vasopressin on phospholipase C activity, intracellular calcium concentration and prostaglandin F2alpha secretion in pig endometrial cells. Reproduction. 2001;121(4):605-12. 73. Hsieh YY, Chang CC, Tsai FJ, Hsu CM, Lin CC, Tsai CH. Angiotensin I-converting enzyme ACE 2350*G and ACE-240*T-related genotypes and alleles are associated with higher susceptibility to endometriosis. Mol Hum Reprod. 2005;11(1):11-4. 74. Hsieh YY, Lee CC, Chang CC, Wang YK, Yeh LS, Lin CS. Angiotensin I-converting enzyme insertion-related genotypes and allele are associated with higher susceptibility of endometriosis and leiomyoma. Mol Reprod Dev. 2007;74(7):808-14. 75. Kowalczyska LJ, Tomasz F, Wojciechowski M, Mordalska A, Pogoda K, Malinowski A. ACE I/D polymorphism in Polish patients with endometriosis. Ginekol Pol. 2011;82(2):102-7. 76. Page-McCaw A, Ewald AJ, Werb Z. Matrix metalloproteinases and the regulation of tissue remodelling. Nat Rev Mol Cell Biol. 2007;8(3): 22133. Review. 77. Kokorine I, Nisolle M, Donnez J, Eeckhout Y, Courtoy PJ, Marbaix E. Expression of interstitial collagenase (matrix metalloproteinase-1) is related to the activity of human endometriotic lesions. Fertil Steril. 1997;68(2):246-51. 78. Cox KE, Piva M, Sharpe-Timms KL. Differential regulation of matrix metalloproteinase-3 gene expression in endometriotic lesions compared with endometrium. Biol Reprod. 2001;65(4):1297-303. 79. Chung HW, Lee JY, Moon HS, Hur SE, Park MH, Wen Y, Polan ML. Matrix metalloproteinase-2, membranous type 1 matrix metalloproteinase, and tissue inhibitor of metalloproteinase-2 expression in ectopic and eutopic endometrium. Fertil Steril. 2002;78(4):787-95. 80. Szamatowicz J, Laudaski P, Tomaszewska I. Matrix metalloproteinase-9 and tissue inhibitor of matrix metalloproteinase-1: a possible role in the pathogenesis of endometriosis. Hum Reprod. 2002 Feb;17(2):284-8. 81. Gilabert-Estells J, Estells A, Gilabert J, Castell R, Espaa F, Falc C, et al. Expression of several components of the plasminogen activator and matrix metalloproteinase systems in endometriosis. Hum Reprod. 2003;18(7):1516-22. 82. Osteen KG, Yeaman GR, Bruner-Tran KL. Matrix metalloproteinases and endometriosis. Semin Reprod Med. 2003;21(2):15564. 83. Shaco-Levy R, Sharabi S, Benharroch D, Piura B, Sion-Vardy N. Matrix metalloproteinases 2 and 9, E-cadherin, and beta-catenin expression in endometriosis, low-grade endometrial carcinoma and non-neoplastic eutopic endometrium. Eur J Obst Gynecol Reprod Biol. 2008;139(2):226-32. 84. Di Carlo C, Bonifacio M, Tommaselli GA, Bifulco G, Guerra G, Nappi C. Metalloproteinases, vascular endothelial growth factor, and angiopoietin 1 and 2 in eutopic and ectopic endometrium. Fertil Steril. 2009;91(6):2315-23. 85. Ye S. Polymorphism in matrix metalloproteinase gene promoters: implication in regulation of gene expression and susceptibility of various diseases. Matrix Biol. 2000;19(7):623-9. 86. Vairaktaris E, Yapijakis C, Yiannopoulos A, Vassiliou S, Serefoglou Z, Vylliotis A, et al. Strong association of the tissue inhibitor of metalloproteinase- 2 polymorphism with an increased risk of oral squamous cell carcinoma in Europeans. Oncol Rep. 2007;17(4):9638. 87. Decock J, Paridaens R, Ye S. Genetic polymorphisms of matrix metalloproteinases in lung, breast and colorectal cancer. Clin Genet. 2008;73(3):197-211. 88. Kang S, Wang Y, Zhang JH, Jin X, Fang SM, Li Y. Single nucleotide polymorphism in the matrix metalloproteinases promoter is associated with susceptibility to endometriosis and adenomyosis. Zhonghua Fu Chan Ke Za Zhi. 2005;40(9):601-4. 89. Shan K, Ying W, Jian-Hui Z, Wei G, Na W, Yan L. The function of the SNP in the MMP1 and MMP3 promoter in susceptibility to endometriosis in China. Mol Hum Reprod. 2005;11(6):423-7. 90. Ferrari MM, Biondi ML, Rossi G, Grijuela B, Gaita S, Perugino G, et al. Analysis of two polymorphisms in the promoter region of matrix metalloproteinase 1 and 3 genes in women with endometriosis. Acta Obstet Gynecol Scand. 2006;85(2):212-7. 91. Borghese B, Chiche JD, Vernerey D, Chenot C, Mir O, Bijaoui G, et al. Genetic polymorphisms of matrix metalloproteinase 12 and 13 genes are implicated in endometriosis progression. Hum Reprod. 2008;23(5):1207-13. 92. Zhao XW, Li Y, Wang N, Zhao J, Li XL, Liu Q, et al. Study on the association of SNPs of MMP-2 and TIMP-2 genes with the risk of endometriosis and adenomyosis. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008;25(3):280-3. 93. Kang S, Zhao XW, Wang N, Chen SC, Zhou RM, Li Y. Association of polymorphisms of the MMP-2 and TIMP-2 genes with the risk of endometriosis in North Chinese women. Fertil Steril. 2008;90(5):2023-9. 94. Saare M, Lamp M, Kaart T, Karro H, Kadastik U, Metspalu A, et al. Polymorphisms in MMP-2 and MMP-9 promoter regions are associated with endometriosis. Fertil Steril. 2010;94(4):1560-3. 95. Shan K, Lian-Fu Z, Hui D, Wei G, Na W, Xia J, et al. Polymorphisms in the promoter regions of the matrix metalloproteinases-7, -9 and the risk of endometriosis and adenomyosis in China. Mol Hum Reprod. 2006;12(1):35-9. 96. Han YJ, Kim HN, Yoon JK, Yi SY, Moon HS, Ahn JJ, et al. Haplotype analysis of the matrix metalloproteinase-9 gene associated with advanced-stage endometriosis. Fertil Steril. 2009;91(6):2324-30.

632

Rev Assoc Med Bras 2012; 58(5):620-632