ESR1 gene variants affect FSHR-depended risk of fibrocystic mastopathy in infertile women

Kornatska A.G.1, Rossokha Z.I.*2, Fishchuk L.Ye.2, Dubenko O.D.1, Medvedieva N.L.2, Flaksemberg М.А.1, Chubei G.V.1, Popova O.F.2, Gorovenko N.G.3

Summary. Background: The infertile women have an increased risk of developing benign and malignant tumors, in particular, breast cancer. Most studies have examined the role of gene variants in the risk of developing breast cancer, but there is little evidence of genetic risk factors for benign tumors. Aim: To assess the combined genetic risk of developing mastopathy in women with FSHR (rs6165, rs6166) and ESR1 (rs9340799, rs2234693) gene variants. Materials and Methods: The study included 87 infertile women (45 with concomitant fibrocystic mastopathy and 42 without mastopathy). Results: For rs9340799 and rs2234693 variants of the ESR1 gene, we did not find any significant differences in the distribution of genotypes in infertile women with or without mastopathy. In patients with mastopathy, there was a reliable increase in the frequency of 307Ala/Ala and 680Ser/Ser genotypes of FSHR gene (χ2 = 6.39, p = 0.012, OR = 4.49 (1.48–13.65)) as compared to patients without mastopathy. In the presence of 307Thr/Thr and 680Asn/Asn genotypes of the FSHR gene, a 4.88-fold reduction of mastopathy risk (χ2 = 8.06, p = 0.005, OR = 0.21(0.07–0.59)) was observed. The frequency of the FSHR and the ESR1 genotypes combinations — 307Thr/Thr+680Asn/Asn+351AG+397TC was significantly decreased in patients with mastopathy. Conclusions: Our study did not find an association of ESR1 gene variants with the risk of developing of mastopathy in infertile women although heterozygous variants of the ESR1 gene enhanced the “protective” effect of FSHR gene variants and reduced the risk of mastopathy.

DOI: 10.32471/exp-oncology.2312-8852.vol-43-no-3.16468

Submitted: June 05, 2021.
*Correspondence: E-mail: zoiroh071@gmail.com
Abbreviations used: FSH — follicle-stimulating hormone;
OR — odds ratio.

The results of several large-scale retrospective cohort studies have confirmed that infertile women have an increased risk of developing benign and malignant tumors, in particular, of breast localization [1–4]. This is attributed primarily to the hormonal imbalance, in particular, of sex hormones in a woman’s body, and possibly to the effects of infertility treatment. The candidate genes that can directly and indirectly affect the functional state of the breast have been already identified [5–7]. However, most studies have examined the role of gene variants in the risk of developing breast cancer, but there is little evidence of genetic risk factors for benign tumors. One previous study reported that ESR1 gene variants modulated the risk of developing both malignant and benign breast tumors in women, but their association with impaired fertility was not investigated [8]. Moreover, we found the association between FSHR gene variants with a risk of infertility and mastopathy [9]. Given the elucidation of the influence of these genes on reproductive processes [10], including replenishment of the follicular reserve [11], and the ability to select optimal protocols for in vitro fertilization [12], the aim of this study was to assess the combined genetic risk of developing mastopathy in women with the ESR1 (rs9340799, rs2234693) and FSHR (rs6165, rs6166) gene variants.

MATERIALS AND METHODS

The study included 87 women with reproductive disorders (long-term infertility over 7 years and infertility that occurred after early reproductive losses). Of these, 45 (51.7%) were women with concomitant fibrocystic mastopathy (code ICD-10 — N60.1.) — group 1, and 42 (48.3%) were women without mastopathy — group 2. Exclusion criteria were as follows: age over 48 years, chronic inflammatory infectious diseases, uterine abnormalities, and cancer. Informed consent was obtained from each participant included in the study. The study was approved by the Ethics Committee of the State Institution “Institute of Pediatrics, Obstetrics and Gynecology of the NAMS of Ukraine”.

The ESR1 (rs9340799, rs2234693) and FSHR (rs6165, rs6166) gene variants were determined using the molecular genetic methods according to previously published protocols [8–10].

Statistical data processing was conducted using Microsoft Excel Pro Plus 2016 and SPSS v.27. Genotype and allele frequencies in the study and comparison groups were compared using the χ2 test. The association of variants of the studied genes with the risk of mastopathy was examined by calculating the odds ratio (OR) within 95% of the confidence interval (CI). Differences were considered reliable for all types of analysis at a significance level (p) less than 0.05.

RESULTS AND DISCUSSION

Previously we have analyzed the influence of FSHR gene variants on the risk of mastopathy and demonstrated that the patients of group 1 had significantly increased frequency of 307Ala/Ala and 680Ser/Ser genotypes in the FSHR gene (χ2 = 6.39, p = 0.012, OR = 4.49 (1.48–13.65)) as compared to patients of group 2. The risk of mastopathy in infertile women with this genotype increased almost by 4.5 times [9]. In the presence of 307Thr/Thr and 680Asn/Asn genotypes of the FSHR gene, a reduced risk of mastopathy 4.88 times was observed (χ2 = 8.06, p = 0.005, OR = 0.21 (0.07–0.59)). It should be noted that the significantly influential variants of the FSHR gene, which we have identified, are characterized by the linked nature of inheritance.

The molecular genetic analysis in the same study groups revealed no differences in the distribution of genotype frequencies for rs9340799 and rs2234693 variants of the ESR1 gene in the groups of women with reproductive disorders with or without mastopathy (Figure). Therefore, ESR1 gene variants does not seem to affect the risk of developing of mastopathy in the studied group of infertile women.

 <i>ESR1</i> gene variants affect <i>FSHR</i> depended risk of fibrocystic mastopathy in infertile women
Figure. The frequencies of genotypes of the ESR1 gene in the comparison groups

To elucidate the possible interaction between ESR1 and FSHR genotypes and the possible modifying effect of the ESR1 gene on the FSHR-depended risk of mastopathy, we investigated the effect of their combinations in infertile women on the risk of developing mastopathy. The data are summarized in the Table.

Table. The frequencies of identified combinations of ESR1 and FSHR genotypes in the comparison groups

FSHR gene variants ESR1 gene variants Group 1 (n = 45) Group 2 (n = 42)
rs6165 rs2234693 rs9340799
307Ala/Ala 397TT 351AA 5 (11.1%) 4 (9.5%)
397TC 351AA 2 (4.4%) 1 (2.4%)
351AG 5 (11.1%) 0 (0.0%)
351GG 1 (2.2%) 0 (0.0%)
397CC 351AG 2 (4.4%) 0 (0.0%)
351GG 2 (4.4%) 0 (0.0%)
307Ala/Thr 397TT 351AA 4 (8.9%) 4 (9.5%)
397TC 351AA 2 (4.4%) 1 (2.4%)
351AG 9 (20.0%) 9 (21.4%)
351GG 0 (0.0%) 1 (2.4%)
397CC 351AA 1 (2.2%) 0 (0.0%)
351AG 3 (6.7%) 0 (0.0%)
351GG 3 (6.7%) 4 (9.5%)
307Thr/Thr 397TT 351AA 1 (2.2%) 2 (4.8%)
397TC 351AA 3 (6.7%) 3 (7.1%)
351AG 2 (4.4%) 9 (21.4%)
397CC 351AA 0 (0.0%) 1 (2.4%)
351AG 0 (0.0%) 3 (7.1%)

Note: Only in combination given in bold, the difference between two groups was significant (p < 0.05).

We found a significant decrease in the frequency of combination of genotypes 307Thr/Thr+680Asn/Asn+351AG+397TC in terms of the FSHR and ESR1 genes in the group of women with reproductive disorders with mastopathy as compared to those without mastopathy (4.4% vs 21.4%, χ2 = 4.43, p = 0.036, OR = 0.17 (0.03–0.84)). Accordingly, in patients of group 1 as compared to group 2, we observed an increased frequency of detection of the combination of genotypes 307Ala/Ala+680Ser/Ser+351AG+397TC in terms of the FSHR and ESR1 (11.1% vs 0.0%, χ2 = 3.11, p = 0.078) due to the linked nature of inheritance, but the differences were not significant. Thus, heterozygous variants of the ESR1 gene enhance the “protective” effect 307Thr/Thr+680Asn/Asn variants of FSHR gene to the development of mastopathy in infertile women (5.86-fold risk reduction).

Recently, there has been an increased interest in determining the factors that lead to the development of benign breast tumors and their role in increasing the risk of breast cancer [13, 14]. A special place in these studies belongs to women with reproductive disorders, in particular, infertility, because hormonal imbalance and hormone therapy used in the treatment of these diseases are predictors of breast cancer. The results of a cross-sectional study conducted by Lundberg et al. [15] showed that women with a history of infertility have increased mammographic density.

In our previous study, we found that the presence of homozygous 307Ala/Ala and 680Ser/Ser genotypes of FSHR gene was associated with the development of mastopathy in infertile women (they were found in almost 40% of infertile patients) as in their presence the risk of mastopathy increased by 4.5 times [9]. However, these variants of the FSHR gene, in particular the presence of the 680Ser allele, are known to be associated with a decreased sensitivity to follicle-stimulating hormone (FSH) and are due to higher levels of serum FSH [11, 16]. On the other hand, the results of studies indicate the role of FSH in the development and progression of benign and malignant neoplasms of the breast [17, 18]. Meanwhile, our results confirm the findings of the above studies.

Our study of these variants of the FSHR gene indicates the possibility of developing pharmacogenetic tests that will be used in the treatment of infertile women. This is clearly confirmed by the existing data that patients with homozygous 680Ser/Ser genotype have a 2-fold increase in the risk of resistance to clomiphene citrate [19], which, on the one hand, is effective in the treatment of some forms of infertility, and on the other hand, may increase the risk of breast cancer [20]. Therefore, the use of this pharmacogenetic test will allow us to develop protocols for personalized prevention and treatment, as well as to optimize the purpose of clomiphene citrate, taking into account genetic characteristics.

We did not find significant differences for the studied variants of ESR1 gene in infertile women. However, our previous studies have shown an association between these variants of ESR1 gene with infertility in Ukrainian married couples. This discrepancy can be explained by different study designs, including the fact that currently, the study group included only infertile women who have frequencies of genotypes for variants in terms of ESR1 gene that differ from the population ones [10].

For infertile women, in whom the markers of genetic risk have been identified, active prophylactic measures may be recommended to reduce the risk of developing benign and malignant breast tumors. In particular, the use of herbal preparations and vitamins that can help normalize hormonal balance is feasible [21–22].

Our study did not find an association of ESR1 gene variants with the risk of developing of mastopathy in infertile women. But heterozygous variants of the ESR1 gene enhanced the protective effect of FSHR gene variants and reduced the risk of mastopathy.

REFERENCES

1. Feng J, Wang J, Zhang Y, et al. The efficacy of complementary and alternative medicine in the treatment of female infertility. Evid Based Complement Alternat Med 2021; 2021: 6634309. doi: 10.1155/2021/6634309.
2. Murugappan G, Li S, Lathi RB, et al. Risk of cancer in infertile women: analysis of US claims data. Hum Reprod 2019; 34: 894–902. doi: 10.1093/humrep/dez018.
3. Williams CL, Jones ME, Swerdlow AJ, et al. Risks of ovarian, breast, and corpus uteri cancer in women treated with assisted reproductive technology in Great Britain, 1991–2010: data linkage study including 2.2 million person years of observation. BMJ 2018; 362: k2644. doi: 10.1136/bmj.k2644.
4. Jensen A, Sharif H, Olsen JH, et al. Risk of breast cancer and gynecologic cancers in a large population of nearly 50,000 infertile Danish women. Am J Epidemiol 2008; 168: 49–57. doi: 10.1093/aje/kwn094.
5. Al-Eitan LN, Rababa’h DM, Alghamdi MA, et al. Association between ESR1, ESR2, HER2, UGT1A4, and UGT2B7 polymorphisms and breast cancer in Jordan: a case-control study. BMC Cancer 2019; 19: 1257. doi: 10.1186/s12885-019-6490-7.
6. Hu X, Jiang L, Tang C, et al. Association of three single nucleotide polymorphisms of ESR1with breast cancer susceptibility: a meta-analysis. J Biomed Res 2017; 31: 213–25. doi: 10.7555/JBR.31.20160087.
7. Henriksen LS, Hagen CP, Assens M, et al. Genetic variations in FSH action affect sex hormone levels and breast tissue size in infant girls: a pilot study. J Clin Endocrinol Metab 2016; 101: 3191-8. doi: 10.1210/jc.2016-1672.
8. Paliychuk OV, Polishchuk LZ, Rossokha ZI, et al. Molecular-genetic models for prognosis of development of tumors of reproductive system in women with family history of cancer. Exp Oncol 2018; 40: 59–67.
9. Kornatskа AG, Gorovenko NG, Dubenko OD, et al. [Genetic risk factor for fibrocystic breast disease in women with infertility]. Health of Woman 2016; 1: 187–91 (in Ukrainian). doi: 10.15574/HW.2016.107.187.
10. Fishchuk L, Rossokha Z, Sheyko L, et al. ESR1 gene related risk in the development of idiopathic infertility and early pregnancy loss in married couples. Georgian Med News 2020; 6: 48–54.
11. Sambor IY, Rossokha ZI, Medvedieva NM, et al. [Genetics aspects of premature ovarian failure development (literature review)]. Obstetrics. Gynecology. Genetics 2018; 4: 52–59 (in Ukrainian).
12. Tatarchuk TF, Hiulmamedova ID, Rossokha ZI, et al. [Pregnancy and childbirth after a cycle of assisted reproductive technologies in patient with a mutation of FSH receptor gene, secondary amenorrhea, uterine hypoplasia and endometrial receptivity disorders (clinical case)]. Reprod Endocrinol 2015; 6: 72–5 (in Russian).
13. Alexa O, Stolnicu S, Horváth E, et al. [The relationship between benign breast proliferation (fibrocystic mastopathy) and the appearance of breast carcinoma]. Rev Med Chir Soc Med Nat Iasi 2000; 104: 101–9 (in Romanian).
14. Schauer K. [Fibrocystic mastopathy as a cancer risk]. Zentralbl Chir 1989; 114: 11–7; discussion 18–9 (in German).
15. Lundberg FE, Johansson AL, Rodriguez-Wallberg K, et al. Association of infertility and fertility treatment with mammographic density in a large screening-based cohort of women: a cross-sectional study. Breast Cancer Res 2016; 18: 36. doi: 10.1186/s13058-016-0693-5.
16. Zalewski G, Wołczyński S, Chyczewski L. Association of rs6166 polymorphism with FSH receptor transcript variants and steroid production in human granulosa cell cultures. Syst Biol Reprod Med 2013; 59: 191–8. doi: 10.3109/19396368.2012.745035.
17. Garde SV, Sheth AR, Joseph R, et al. Occurrence and de novo biosynthesis of follicle stimulating hormone (FSH) in benign and malignant conditions of human breast. Cancer Lett 1993; 75: 1–9. doi: 10.1016/0304-3835(93)90200-s.
18. Zhou J, Chen Y, Huang Y, et al. Serum follicle-stimulating hormone level is associated with human epidermal growth factor receptor type 2 and Ki67 expression in post-menopausal females with breast cancer. Oncol Lett 2013; 6: 1128–32. doi: 10.3892/ol.2013.1516.
19. Valkenburg O, van Santbrink EJ, König TE, et al. Follicle-stimulating hormone receptor polymorphism affects the outcome of ovulation induction in normogonadotropic (World Health Organization class 2) anovulatory subfertility. Fertil Steril 2015; 103: 1081-8.e3. doi: 10.1016/j.fertnstert.2015.01.002.
20. Lerner-Geva L, Keinan-Boker L, Blumstein T, et al. Infertility, ovulation induction treatments and the incidence of breast cancer-a historical prospective cohort of Israeli women. Breast Cancer Res Treat 2006; 100: 201–12. doi: 10.1007/s10549-006-9238-4.
21. Kwon CY, Cho IH, Park KS. Therapeutic effects and mechanisms of herbal medicines for treating polycystic ovary syndrome: a review. Front Pharmacol 2020; 11: 1192. doi: 10.3389/fphar.2020.01192.
22. Jin J, Hu QY, Xu WW, et al. Tanshinone IIA attenuates estradiol-induced polycystic ovarian syndrome in mice by ameliorating FSHR expression in the ovary. Exp Ther Med 2019; 17: 3501–8. doi: 10.3892/etm.2019.7352.

ВАРІАНТИ ГЕНА ESR1 ВПЛИВАЮТЬ НА FSHR-ЗАЛЕЖНИЙ РИЗИК РОЗВИТКУ МАСТОПАТІЇ У БЕЗПЛІДНИХ ЖІНОК

А.Г. Корнацька1, З.І. Россоха2, *, Л.Є. Фіщук2, О.Д. Дубенко1, Н.Л.Медведєва2, М.А. Флаксемберг1, Г.В. Чубей1, О.Ф. Попова2, Н.Г. Горовенко3

1Державна установа “Інститут педіатрії, акушерства і гінекології імені академіка О.М. Лук’янової НАМН України”, м. Київ, 04050, Україна
2Державний заклад “Референс-центр з молекулярної діагностики Міністерства охорони здоров’я України”, м. Київ, 04112, Україна
3Національний університет охорони здоров’я України імені П.Л. Шупика, м. Київ, 04112, Україна

Резюме. Стан питання: У жінок з безпліддям відмічають підвищений ризик розвитку доброякісних та злоякісних новоутворень, зокрема, локалізованих у молочній залозі. Більшість досліджень присвячені вивченню ролі варіантів генів в ризику розвитку раку молочної залози, але практично відсутні дані про генетичні чинники ризику виникнення доброякісних новоутворень. Мета: Оцінка комбінованого генетичного ризику розвитку мастопатії у жінок з варіантами генів ESR1 (rs9340799, rs2234693) та FSHR (rs6165, rs6166) для формування стратегії персоналізованих клінічних рішень при лікуванні безпліддя. Матеріали та методи: До дослідження було залучено 87 жінок із безпліддям. Із них — 45 (51.7%) жінок із супутньою фіброзно-кістозною мастопатією та 42 (48.3%) жінки без мастопатії. Результати: Для варіантів rs9340799 та rs2234693 гена ESR1 нами не було виявлено жодних вірогідних відмінностей у розподілі генотипів у безплідних жінок двох груп порівняння. У пацієнток з мастопатією було відмічено вірогідне підвищення частоти генотипів 307Ala/Ala та 680Ser/Ser гена FSHR (χ2 = 6,39, р = 0,012, OR = 4,49 (1,48–13,65)) порівняно з особами без мастопатії. А за наявності генотипів 307Thr/Thr та 680Asn/Asn гена FSHR було виявлено зниження ризику розвитку­ мастопатії у 4,88 раза (χ2 = 8,06, р = 0,005, OR = 0,21 (0,07–0,59)). Частота поєднання генотипів за генами FSHR та ESR1 -307Thr/Thr+680Asn/Asn+351AG+397TC була значущо знижена у пацієнтів з мастопатією порівняно з пацієнтами без мастопатії (4,4% проти 21,4%, χ2 = 4,43, p = 0,036, OR = 0,17 (0,03–0,84)). Висновки: У нашому дослідженні не було виявлено асоціацій варіантів гена ESR1 з ризиком розвитку мастопатії у жінок з безпліддям. Але гетерозиготні варіанти гена ESR1 посилювали “протективний” ефект варіантів гена FSHR і знижували ризик розвитку мастопатії.

Ключові слова: мастопатія, безпліддя, FSHR, ESR1.

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