| Literature DB >> 32270196 |
Vera Chesnokova1, Shlomo Melmed1.
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). © Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: DNA damage response; DNA repair; IGF1; gonadotropins; growth hormone; αMSH
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Year: 2020 PMID: 32270196 PMCID: PMC7279704 DOI: 10.1210/endrev/bnaa009
Source DB: PubMed Journal: Endocr Rev ISSN: 0163-769X Impact factor: 19.871