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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Language: | English |
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Frontiers Media S.A.
2018-12-01
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Series: | Frontiers in Endocrinology |
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Online Access: | https://www.frontiersin.org/article/10.3389/fendo.2018.00772/full |
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Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
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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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 |