The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.

Women with advanced maternal age exhibit low anti-Müllerian hormone (AMH) levels and an altered follicular environment, which is associated with poor oocyte quality and embryonic developmental potential. However, the underlying mechanism is poorly understood. The present study aimed to assesswhether...

Full description

Bibliographic Details
Main Authors: Xu-Lei Sun, Hao Jiang, Dong-Xu Han, Yao Fu, Jian-Bo Liu, Yan Gao, Shu-Min Hu, Bao Yuan, Jia-Bao Zhang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6147527?pdf=render
id doaj-e6bb8c546d0e4ac8adea46209a6b3b80
record_format Article
spelling doaj-e6bb8c546d0e4ac8adea46209a6b3b802020-11-25T01:00:12ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01139e020452410.1371/journal.pone.0204524The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.Xu-Lei SunHao JiangDong-Xu HanYao FuJian-Bo LiuYan GaoShu-Min HuBao YuanJia-Bao ZhangWomen with advanced maternal age exhibit low anti-Müllerian hormone (AMH) levels and an altered follicular environment, which is associated with poor oocyte quality and embryonic developmental potential. However, the underlying mechanism is poorly understood. The present study aimed to assesswhether aging patients exhibit an activated DNA double-strandbreak (DSB) repair pathway in cumulus cells and thus, an association with poor outcomes after in vitro fertilization-embryo transfer (IVF-ET) treatment. Cumulus cells from young (≤29 y) and aging (≥37 y) human female patients were collected after oocyte retrieval. Our results indicated that aging patients showed a higher rate of γ-H2AX-positive cells than in young patients (24.33±4.55 vs.12.40±2.31, P<0.05). We also found that the mRNA expression levels of BRCA1, ATM, MRE11 and RAD51 were significantly elevated in aging cumulus cells. Accordingly, significantly increased protein levels of phospho-H2AX, BRCA1, ATM, MRE11 and RAD51 could be observed in aging cumulus cells. Moreover, aging cumulus cells showed a more frequent occurrence of early apoptosis than young cumulus cells. This study found that increases in DSBs and the activation of the repair pathway are potential indicators that may be used to predictoutcomes after IVF-ET treatment.http://europepmc.org/articles/PMC6147527?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Xu-Lei Sun
Hao Jiang
Dong-Xu Han
Yao Fu
Jian-Bo Liu
Yan Gao
Shu-Min Hu
Bao Yuan
Jia-Bao Zhang
spellingShingle Xu-Lei Sun
Hao Jiang
Dong-Xu Han
Yao Fu
Jian-Bo Liu
Yan Gao
Shu-Min Hu
Bao Yuan
Jia-Bao Zhang
The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.
PLoS ONE
author_facet Xu-Lei Sun
Hao Jiang
Dong-Xu Han
Yao Fu
Jian-Bo Liu
Yan Gao
Shu-Min Hu
Bao Yuan
Jia-Bao Zhang
author_sort Xu-Lei Sun
title The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.
title_short The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.
title_full The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.
title_fullStr The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.
title_full_unstemmed The activated DNA double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.
title_sort activated dna double-strand break repair pathway in cumulus cells from aging patients may be used as a convincing predictor of poor outcomes after in vitro fertilization-embryo transfer treatment.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Women with advanced maternal age exhibit low anti-Müllerian hormone (AMH) levels and an altered follicular environment, which is associated with poor oocyte quality and embryonic developmental potential. However, the underlying mechanism is poorly understood. The present study aimed to assesswhether aging patients exhibit an activated DNA double-strandbreak (DSB) repair pathway in cumulus cells and thus, an association with poor outcomes after in vitro fertilization-embryo transfer (IVF-ET) treatment. Cumulus cells from young (≤29 y) and aging (≥37 y) human female patients were collected after oocyte retrieval. Our results indicated that aging patients showed a higher rate of γ-H2AX-positive cells than in young patients (24.33±4.55 vs.12.40±2.31, P<0.05). We also found that the mRNA expression levels of BRCA1, ATM, MRE11 and RAD51 were significantly elevated in aging cumulus cells. Accordingly, significantly increased protein levels of phospho-H2AX, BRCA1, ATM, MRE11 and RAD51 could be observed in aging cumulus cells. Moreover, aging cumulus cells showed a more frequent occurrence of early apoptosis than young cumulus cells. This study found that increases in DSBs and the activation of the repair pathway are potential indicators that may be used to predictoutcomes after IVF-ET treatment.
url http://europepmc.org/articles/PMC6147527?pdf=render
work_keys_str_mv AT xuleisun theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT haojiang theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT dongxuhan theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT yaofu theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT jianboliu theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT yangao theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT shuminhu theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT baoyuan theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT jiabaozhang theactivateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT xuleisun activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT haojiang activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT dongxuhan activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT yaofu activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT jianboliu activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT yangao activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT shuminhu activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT baoyuan activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
AT jiabaozhang activateddnadoublestrandbreakrepairpathwayincumuluscellsfromagingpatientsmaybeusedasaconvincingpredictorofpooroutcomesafterinvitrofertilizationembryotransfertreatment
_version_ 1725214537843474432