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卵母细胞和胚胎中的DNA修复与对精子DNA损伤的反应以及辅助生殖技术中的潜在后果:一项系统综述

DNA repair and response to sperm DNA damage in oocytes and embryos, and the potential consequences in ART: a systematic review.

作者信息

Newman H, Catt S, Vining B, Vollenhoven B, Horta F

机构信息

Education Program in Reproduction and Development, Department of Obstetrics and Gynecology, Monash University, Melbourne, VIC, Australia.

Centre for Endocrinology and Metabolism, Hudson Institute of Medical Research, Melbourne, VIC, Australia.

出版信息

Mol Hum Reprod. 2022 Jan 4;28(1). doi: 10.1093/molehr/gaab071.

Abstract

Sperm DNA damage is considered a predictive factor for the clinical outcomes of patients undergoing ART. Laboratory evidence suggests that zygotes and developing embryos have adopted specific response and repair mechanisms to repair DNA damage of paternal origin. We have conducted a systematic review in accordance with guidelines from Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) to identify and review the maternal mechanisms used to respond and repair sperm DNA damage during early embryonic development, how these mechanisms operate and their potential clinical implications. The literature search was conducted in Ovid MEDLINE and Embase databases until May 2021. Out of 6297 articles initially identified, 36 studies were found to be relevant through cross referencing and were fully extracted. The collective evidence in human and animal models indicate that the early embryo has the capacity to repair DNA damage within sperm by activating maternally driven mechanisms throughout embryonic development. However, this capacity is limited and likely declines with age. The link between age and decreased DNA repair capacity could explain decreased oocyte quality in older women, poor reproductive outcomes in idiopathic cases and patients who present high sperm DNA damage. Ultimately, further understanding mechanisms underlying the maternal repair of sperm DNA damage could lead to the development of targeted therapies to decrease sperm DNA damage, improved oocyte quality to combat incoming DNA insults or lead to development of methodologies to identify individual spermatozoa without DNA damage.

摘要

精子DNA损伤被认为是接受辅助生殖技术(ART)患者临床结局的一个预测因素。实验室证据表明,受精卵和发育中的胚胎已采用特定的反应和修复机制来修复父源DNA损伤。我们按照系统评价和Meta分析的首选报告项目(PRISMA)指南进行了一项系统评价,以识别和综述早期胚胎发育过程中母体用于应对和修复精子DNA损伤的机制、这些机制如何运作及其潜在的临床意义。文献检索在Ovid MEDLINE和Embase数据库中进行,直至2021年5月。在最初识别的6297篇文章中,通过交叉引用发现36项研究相关并进行了完整提取。人和动物模型的综合证据表明,早期胚胎有能力在整个胚胎发育过程中通过激活母体驱动的机制来修复精子内的DNA损伤。然而,这种能力是有限的,并且可能会随着年龄的增长而下降。年龄与DNA修复能力下降之间的联系可以解释老年女性卵母细胞质量下降、特发性病例以及精子DNA损伤高的患者生殖结局不良的原因。最终,进一步了解母体修复精子DNA损伤的潜在机制可能会促成靶向治疗的发展,以减少精子DNA损伤、改善卵母细胞质量以抵抗传入的DNA损伤,或促成识别无DNA损伤个体精子的方法的开发。

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