1] Mechanisms of Cancer, Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland [2] Oncology, Novartis Institutes for Biomedical Research, Basel, Switzerland.
Mechanisms of Cancer, Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.
Oncogene. 2015 Jul;34(28):3617-26. doi: 10.1038/onc.2014.314. Epub 2014 Sep 29.
The introduction of targeted therapy promised personalized and efficacious cancer treatments. However, although some targeted therapies have undoubtedly improved prognosis and outcome for specific cancer patients, the recurrent problem of therapeutic resistance subdues present revolutionary claims in this field. The plasticity of tumor cells leads to the development of drug resistance by distinct mechanisms: (1) mutations in the target, (2) reactivation of the targeted pathway, (3) hyperactivation of alternative pathways and (4) cross-talk with the microenvironment. Moreover, the intra-tumor heterogeneity of most tumors can also limit therapeutic response. Interestingly, the early identification of some mechanisms of resistance led to the use of alternative agents that improved clinical benefit, demonstrating that an understanding of the molecular mechanisms driving resistance to specific therapies is of paramount importance. Here we review the most generalized mechanisms of resistance to targeted therapies, together with some experimental strategies employed to identify such mechanisms. Therapeutic failure is not an option and we need to understand the dynamics of tumor adaptation in order to adequately adjust therapies; in essence 'to fight fire with fire'.
靶向治疗的引入承诺为癌症患者提供个性化和有效的治疗。然而,尽管一些靶向治疗无疑改善了特定癌症患者的预后和结果,但治疗耐药性的反复出现问题削弱了该领域目前的革命性主张。肿瘤细胞的可塑性通过不同的机制导致药物耐药性的发展:(1)靶标中的突变,(2)靶向途径的重新激活,(3)替代途径的过度激活,以及(4)与微环境的串扰。此外,大多数肿瘤的肿瘤内异质性也可能限制治疗反应。有趣的是,一些耐药机制的早期鉴定导致了使用改善临床获益的替代药物的应用,这表明了解驱动对特定治疗耐药的分子机制至关重要。在这里,我们综述了靶向治疗耐药的最常见机制,以及一些用于鉴定这些机制的实验策略。治疗失败不是一种选择,我们需要了解肿瘤适应的动态,以便适当地调整治疗;本质上是“以毒攻毒”。