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肽激素对 DNA 损伤反应的调节。

Peptide Hormone Regulation of DNA Damage Responses.

机构信息

Pituitary Center, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.

出版信息

Endocr Rev. 2020 Jul 1;41(4). doi: 10.1210/endrev/bnaa009.

Abstract

DNA damage response (DDR) and DNA repair pathways determine neoplastic cell transformation and therapeutic responses, as well as the aging process. Altered DDR functioning results in accumulation of unrepaired DNA damage, increased frequency of tumorigenic mutations, and premature aging. Recent evidence suggests that polypeptide hormones play a role in modulating DDR and DNA damage repair, while DNA damage accumulation may also affect hormonal status. We review the available reports elucidating involvement of insulin-like growth factor 1 (IGF1), growth hormone (GH), α-melanocyte stimulating hormone (αMSH), and gonadotropin-releasing hormone (GnRH)/gonadotropins in DDR and DNA repair as well as the current understanding of pathways enabling these actions. We discuss effects of DNA damage pathway mutations, including Fanconi anemia, on endocrine function and consider mechanisms underlying these phenotypes. (Endocrine Reviews 41: 1 - 19, 2020).

摘要

DNA 损伤反应 (DDR) 和 DNA 修复途径决定了肿瘤细胞的转化和治疗反应,以及衰老过程。DDR 功能的改变会导致未修复的 DNA 损伤积累、致癌突变的频率增加和过早衰老。最近的证据表明,多肽激素在调节 DDR 和 DNA 损伤修复中发挥作用,而 DNA 损伤的积累也可能影响激素状态。我们回顾了现有的报告,这些报告阐明了胰岛素样生长因子 1 (IGF1)、生长激素 (GH)、α-黑色素细胞刺激素 (αMSH)和促性腺激素释放激素 (GnRH)/促性腺激素在 DDR 和 DNA 修复中的作用,以及使这些作用成为可能的途径的当前理解。我们讨论了 DNA 损伤途径突变,包括范可尼贫血,对内分泌功能的影响,并考虑了这些表型的潜在机制。(内分泌评论 41: 1-19, 2020)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6df4/7279704/938942e82d1b/edrv_41_4_bnaa009_f5.jpg

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