| Literature DB >> 36190612 |
Ning Bao1, Jiguang Han2,3, Huimin Zhou1.
Abstract
Damage-specific DNA-binding protein 2 (DDB2) was initially identified as a component of the damage-specific DNA-binding heterodimeric complex, which cooperates with other proteins to repair UV-induced DNA damage. DDB2 is involved in the occurrence and development of cancer by affecting nucleotide excision repair (NER), cell apoptosis, and premature senescence. DDB2 also affects the sensitivity of cancer cells to radiotherapy and chemotherapy. In addition, a recent study found that DDB2 is a pathogenic gene for hepatitis and encephalitis. In recent years, there have been few relevant literature reports on DDB2, so there is still room for further research about it. In this paper, the molecular mechanisms of different biological processes involving DDB2 are reviewed in detail to provide theoretical support for research on drugs that can target DDB2.Entities:
Keywords: Apoptosis; Cancer; Chemoradiotherapy; Damage-specific DNA-binding protein 2 (DDB2); Nucleotide excision repair (NER); Premature senescence
Year: 2022 PMID: 36190612 DOI: 10.1007/s11033-022-07963-4
Source DB: PubMed Journal: Mol Biol Rep ISSN: 0301-4851 Impact factor: 2.742