| Literature DB >> 32319570 |
Zhou Zhang1, Lixia Zheng1, Yang Yu1, Jinying Wu1, Fan Yang1, Yingxi Xu1, Qiqiang Guo1, Xuan Wu1, Sunrun Cao1, Liu Cao1, Xiaoyu Song1.
Abstract
Sterile alpha motif and histidine/aspartic acid domain‑containing protein 1 (SAMHD1), the only deoxynucleotide triphosphate (dNTP) hydrolase in eukaryotes, plays a crucial role in regulating the dynamic balance and ratio of cellular dNTP pools. Furthermore, SAMHD1 has been reported to be involved in the pathological process of several diseases. Homozygous SAMHD1 mutations have been identified in immune system disorders, such as autoimmune disease Aicardi‑Goutières syndrome (AGS), whose primary pathogenesis is associated with the abnormal accumulation and disproportion of dNTPs. SAMHD1 is also considered to be an intrinsic virus‑restriction factor by suppressing the viral infection process, including reverse transcription, replication, packaging and transmission. In addition, SAMHD1 has been shown to promote genome integrity during homologous recombination following DNA damage, thus being considered a promising candidate for oncotherapy applications. The present review summarizes the molecular mechanisms of SAMHD1 regarding the regulation of dNTP homeostasis and DNA damage response. Additionally, its potential effects on tumorigenesis and oncotherapy are reported.Entities:
Year: 2020 PMID: 32319570 DOI: 10.3892/ijo.2020.4988
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650