Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With Endometriosis

Background: Repair of DNA double strand break (DSB) is an important mechanism for maintaining genetic stability during a DNA damage event. Although, a growing body of recent evidence suggests that DNA DSBs and related repair mechanisms may be important in ovarian aging and in various cancers, there...

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Main Authors: Young Sik Choi, Ji Hyun Park, Jae Hoon Lee, Jeong-Kee Yoon, Bo Hyon Yun, Joo Hyun Park, Seok Kyo Seo, Hak-Joon Sung, Hyun-Soo Kim, SiHyun Cho, Byung Seok Lee
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-12-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fendo.2018.00772/full
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language English
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author Young Sik Choi
Young Sik Choi
Ji Hyun Park
Ji Hyun Park
Jae Hoon Lee
Jae Hoon Lee
Jeong-Kee Yoon
Bo Hyon Yun
Bo Hyon Yun
Joo Hyun Park
Joo Hyun Park
Seok Kyo Seo
Seok Kyo Seo
Hak-Joon Sung
Hyun-Soo Kim
SiHyun Cho
SiHyun Cho
Byung Seok Lee
Byung Seok Lee
spellingShingle Young Sik Choi
Young Sik Choi
Ji Hyun Park
Ji Hyun Park
Jae Hoon Lee
Jae Hoon Lee
Jeong-Kee Yoon
Bo Hyon Yun
Bo Hyon Yun
Joo Hyun Park
Joo Hyun Park
Seok Kyo Seo
Seok Kyo Seo
Hak-Joon Sung
Hyun-Soo Kim
SiHyun Cho
SiHyun Cho
Byung Seok Lee
Byung Seok Lee
Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With Endometriosis
Frontiers in Endocrinology
endometriosis
ovarian reserve
double stranded DNA break
BRCA1 gene
gamma-H2AX
author_facet Young Sik Choi
Young Sik Choi
Ji Hyun Park
Ji Hyun Park
Jae Hoon Lee
Jae Hoon Lee
Jeong-Kee Yoon
Bo Hyon Yun
Bo Hyon Yun
Joo Hyun Park
Joo Hyun Park
Seok Kyo Seo
Seok Kyo Seo
Hak-Joon Sung
Hyun-Soo Kim
SiHyun Cho
SiHyun Cho
Byung Seok Lee
Byung Seok Lee
author_sort Young Sik Choi
title Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With Endometriosis
title_short Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With Endometriosis
title_full Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With Endometriosis
title_fullStr Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With Endometriosis
title_full_unstemmed Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With Endometriosis
title_sort association between impairment of dna double strand break repair and decreased ovarian reserve in patients with endometriosis
publisher Frontiers Media S.A.
series Frontiers in Endocrinology
issn 1664-2392
publishDate 2018-12-01
description Background: Repair of DNA double strand break (DSB) is an important mechanism for maintaining genetic stability during a DNA damage event. Although, a growing body of recent evidence suggests that DNA DSBs and related repair mechanisms may be important in ovarian aging and in various cancers, there are few reports in endometriosis. We, therefore, examined expression levels of genes pertaining to DNA DSB repair in patients with endometriosis to assess the potential effects on ovarian reserves.Materials and methods: A total of 69 women undergoing laparoscopic surgery for endometriosis and other benign conditions was included; endometriosis group (n = 38) vs. controls (n = 31). DNA DSBs in endometrial and ovarian tissues of both groups were compared via immunohistochemistry, aimed at γ-H2AX expression. To gauge genotoxin-induced DNA DSBs in endometrial stromal cells, γ-H2AX expression was determined by western blot after H2O2 treatment of cultured endometrial stromal cells (endometriosis group and controls) and Ishikawa cell-line cultures. Endometrial and ovarian tissue levels of BRCA1, BRCA2, Rad51, and ATM (ataxia-telangiectasia mutated) mRNA expression were also compared. Correlations between expression levels of genes of interest and serum anti-müllerian hormone (AMH) levels were assessed as well.Results: Expression of γ-H2AX in immunostained endometrial and ovarian tissue preparations was greater in the endometriosis group, compared with controls. After H2O2 treatment, γ-H2AX expression levels were also significantly greater in cultured stromal cells of the endometriosis group and in the Ishikawa cell line than in controls. Endometrial expression of BRCA1 and Rad51 mRNA proved significantly lower in the endometriosis group (vs. controls), as did ovarian expression of BRCA1 and BRCA2 mRNA. Serum AMH concentration showed a significant correlation with ovarian BRCA1 mRNA expression in women with endometriosis (p = 0.03).Conclusions: In women with endometriosis, expression levels of various genes implicated in DSB repair are decreased and ovarian BRCA1 expression correlates with
topic endometriosis
ovarian reserve
double stranded DNA break
BRCA1 gene
gamma-H2AX
url https://www.frontiersin.org/article/10.3389/fendo.2018.00772/full
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spelling doaj-02436531421d4bc0845a9742a57bcc1f2020-11-24T21:15:37ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922018-12-01910.3389/fendo.2018.00772433443Association Between Impairment of DNA Double Strand Break Repair and Decreased Ovarian Reserve in Patients With EndometriosisYoung Sik Choi0Young Sik Choi1Ji Hyun Park2Ji Hyun Park3Jae Hoon Lee4Jae Hoon Lee5Jeong-Kee Yoon6Bo Hyon Yun7Bo Hyon Yun8Joo Hyun Park9Joo Hyun Park10Seok Kyo Seo11Seok Kyo Seo12Hak-Joon Sung13Hyun-Soo Kim14SiHyun Cho15SiHyun Cho16Byung Seok Lee17Byung Seok Lee18Department of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Medical Engineering, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Medical Engineering, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, South KoreaInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, South KoreaBackground: Repair of DNA double strand break (DSB) is an important mechanism for maintaining genetic stability during a DNA damage event. Although, a growing body of recent evidence suggests that DNA DSBs and related repair mechanisms may be important in ovarian aging and in various cancers, there are few reports in endometriosis. We, therefore, examined expression levels of genes pertaining to DNA DSB repair in patients with endometriosis to assess the potential effects on ovarian reserves.Materials and methods: A total of 69 women undergoing laparoscopic surgery for endometriosis and other benign conditions was included; endometriosis group (n = 38) vs. controls (n = 31). DNA DSBs in endometrial and ovarian tissues of both groups were compared via immunohistochemistry, aimed at γ-H2AX expression. To gauge genotoxin-induced DNA DSBs in endometrial stromal cells, γ-H2AX expression was determined by western blot after H2O2 treatment of cultured endometrial stromal cells (endometriosis group and controls) and Ishikawa cell-line cultures. Endometrial and ovarian tissue levels of BRCA1, BRCA2, Rad51, and ATM (ataxia-telangiectasia mutated) mRNA expression were also compared. Correlations between expression levels of genes of interest and serum anti-müllerian hormone (AMH) levels were assessed as well.Results: Expression of γ-H2AX in immunostained endometrial and ovarian tissue preparations was greater in the endometriosis group, compared with controls. After H2O2 treatment, γ-H2AX expression levels were also significantly greater in cultured stromal cells of the endometriosis group and in the Ishikawa cell line than in controls. Endometrial expression of BRCA1 and Rad51 mRNA proved significantly lower in the endometriosis group (vs. controls), as did ovarian expression of BRCA1 and BRCA2 mRNA. Serum AMH concentration showed a significant correlation with ovarian BRCA1 mRNA expression in women with endometriosis (p = 0.03).Conclusions: In women with endometriosis, expression levels of various genes implicated in DSB repair are decreased and ovarian BRCA1 expression correlates withhttps://www.frontiersin.org/article/10.3389/fendo.2018.00772/fullendometriosisovarian reservedouble stranded DNA breakBRCA1 genegamma-H2AX