机制(生物学)
染色体不稳定性
药品
非整倍体
基因组不稳定性
生物
癌症研究
癌症
染色体
点突变
基因
突变
抗药性
遗传学
生物信息学
药理学
DNA
DNA损伤
哲学
认识论
作者
Devon A. Lukow,Jason M. Sheltzer
标识
DOI:10.1016/j.trecan.2021.09.002
摘要
High levels of aneuploidy and chromosomal instability (CIN) are correlated with poor patient outcomes, though the mechanism(s) underlying this relationship have not been established. Recent evidence has demonstrated that chromosome copy number changes can function as point mutation-independent sources of drug resistance in cancer, which may partially explain this clinical association. CIN generates intratumoral heterogeneity in the form of gene dosage alterations, upon which the selective pressures induced by drug treatments can act. Thus, although CIN and aneuploidy impair cell fitness under most conditions, CIN can augment cellular adaptability, establishing CIN as a bet-hedging mechanism in tumor evolution. CIN may also endow cancers with unique vulnerabilities, which could be exploited therapeutically to achieve better patient outcomes.
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