G-quadruplex-mediated genomic instability drives SNVs in cancer

被引:2
|
作者
Richl, Tilmann [1 ]
Kuper, Jochen [1 ]
Kisker, Caroline [1 ]
机构
[1] Univ Wurzburg, Rudolf Virchow Ctr Integrat & Translat Bioimaging, D-97080 Wurzburg, Germany
关键词
DNA-DAMAGE; SMALL-MOLECULE; MOTIFS; REPLICATION; DEFICIENT; HELICASES; SEQUENCE; TARGETS; MYC; MAP;
D O I
10.1093/nar/gkae098
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G-quadruplex (G4s) DNA structures have been implicated in inducing genomic instability and contributing to cancer development. However, the relationship between G4s and cancer-related single nucleotide variants (cSNVs) in clinical settings remains unclear. In this large-scale study, we integrated experimentally validated G4s with genomic cSNVs from 13480 cancer patients to investigate the spatial association of G4s with the cellular cSNV landscape. Our findings demonstrate an increase in local genomic instability with increasing local G4 content in cancer patients, suggesting a potential role for G4s in driving cSNVs. Notably, we observed distinct spatial patterns of cSNVs and common single nucleotide variants (dbSNVs) in relation to G4s, implying different mechanisms for their generation and accumulation. We further demonstrate large, cancer-specific differences in the relationship of G4s and cSNVs, which could have important implications for a new class of G4-stabilizing cancer therapeutics. Moreover, we show that high G4-content can serve as a prognostic marker for local cSNV density and patient survival rates. Our findings underscore the importance of considering G4s in cancer research and highlight the need for further investigation into the underlying molecular mechanisms of G4-mediated genomic instability, especially in the context of cancer. Graphical Abstract
引用
收藏
页码:2198 / 2211
页数:14
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