Department of Oncology Biomarker Development, Genentech, Inc., South San Francisco, CA, USA.
Future Oncol. 2012 Aug;8(8):999-1014. doi: 10.2217/fon.12.86.
Drugs that target genomically defined vulnerabilities in human tumors have now been clinically validated as effective cancer therapies. However, the relatively rapid acquisition of resistance to such treatments that is observed in virtually all cases significantly limits their utility and remains a substantial challenge to the clinical management of advanced cancers. As molecular mechanisms of resistance have begun to be elucidated, new strategies to overcome or prevent the development of resistance have begun to emerge. In some cases, specific mutational mechanisms contribute directly to acquired drug resistance, and in other cases it appears that nonmutational and possibly epigenetic mechanisms play a significant role. This article discusses the various genetic and nongenetic mechanisms of acquired drug resistance that have been reported in the context of 'rationally targeted' drug therapies.
目前,针对人类肿瘤中基因组定义的弱点的药物已被临床验证为有效的癌症疗法。然而,几乎所有情况下都观察到对这些治疗的相对快速获得性耐药,这大大限制了它们的效用,并仍然是对晚期癌症的临床管理的重大挑战。随着耐药性的分子机制开始被阐明,克服或预防耐药性发展的新策略开始出现。在某些情况下,特定的突变机制直接导致获得性药物耐药性,而在其他情况下,非突变和可能的表观遗传机制似乎起着重要作用。本文讨论了在“合理靶向”药物治疗背景下报道的获得性药物耐药性的各种遗传和非遗传机制。