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精子表观基因组能否成为评估男性不育的诊断工具?

Could the sperm epigenome become a diagnostic tool for evaluation of the infertile man?

机构信息

Asl Bari, Andrology Outpatients Clinic, Bari, Italy.

Center for Reproductive Biology, School of Biological Sciences, Washington State University, Pullman, WA, USA.

出版信息

Hum Reprod. 2024 Mar 1;39(3):478-485. doi: 10.1093/humrep/dead266.

Abstract

Although male infertility is currently diagnosed when abnormal sperm parameters are found, the poor predictive ability of sperm parameters on natural fecundity and medically assisted reproduction outcome poses the need for improved diagnostic techniques for male infertility. The accumulating evidence about the role played by the sperm epigenome in modulation of the early phases of embryonic development has led researchers to focus on the epigenetic mechanisms within the sperm epigenome to find new molecular markers of male infertility. Indeed, sperm epigenome abnormalities could explain some cases of unexplained male infertility in men showing normal sperm parameters and were found to be associated with poor embryo development in IVF cycles. The present mini-review summarizes the current knowledge about this interesting topic, starting from a description of the epigenetic mechanisms of gene expression regulation (i.e. DNA methylation, histone modifications, and non-coding RNAs' activity). We also discuss possible mechanisms by which environmental factors might cause epigenetic changes in the human germline and affect embryonic development, as well as subsequent generations' phenotypes. Studies demonstrating sperm epigenome abnormalities in men with male infertility are reviewed, with particular emphasis on those with the more severe form of spermatogenic dysfunction. Observations demonstrate that the diagnostic and prognostic efficacy of sperm epigenome evaluation will help facilitate the management of men with male factor infertility.

摘要

尽管目前男性不育症是通过发现异常的精子参数来诊断的,但精子参数对自然生育力和医学辅助生殖结果的预测能力较差,这就需要改进男性不育症的诊断技术。越来越多的证据表明,精子表观基因组在调节胚胎早期发育中起着重要作用,这促使研究人员关注精子表观基因组中的表观遗传机制,以寻找男性不育症的新分子标志物。事实上,精子表观基因组异常可以解释一些精子参数正常的男性不明原因不育症病例,并且与 IVF 周期中胚胎发育不良有关。本综述文章从描述基因表达调控的表观遗传机制(即 DNA 甲基化、组蛋白修饰和非编码 RNA 的活性)开始,总结了这一有趣主题的最新知识。我们还讨论了环境因素可能通过哪些机制引起人类生殖系的表观遗传变化,并影响胚胎发育以及后代的表型。本文综述了男性不育症患者精子表观基因组异常的研究,特别强调了那些更严重的生精功能障碍患者。研究结果表明,精子表观基因组评估的诊断和预后效能将有助于男性因素不育症患者的管理。

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