Friedman Ran
Department of Chemistry and Biomedical Sciences, Linnæus University, Kalmar, Sweden.
Oncotarget. 2016 Mar 15;7(11):11746-55. doi: 10.18632/oncotarget.7459.
Targeted therapies have revolutionized cancer treatment. Unfortunately, their success is limited due to the development of drug resistance within the tumor, which is an evolutionary process. Understanding how drug resistance evolves is a prerequisite to a better success of targeted therapies. Resistance is usually explained as a response to evolutionary pressure imposed by treatment. Thus, evolutionary understanding can and should be used in the design and treatment of cancer. In this article, drug-resistance to targeted therapies is reviewed from an evolutionary standpoint. The concept of apoptosis-induced compensatory proliferation (AICP) is developed. It is shown that AICP helps to explain some of the phenomena that are observed experimentally in cancers. Finally, potential drug targets are suggested in light of AICP.
靶向治疗彻底改变了癌症治疗方式。不幸的是,由于肿瘤内耐药性的产生,其疗效受到限制,而这是一个进化过程。了解耐药性如何演变是靶向治疗取得更好疗效的先决条件。耐药性通常被解释为对治疗施加的进化压力的一种反应。因此,进化方面的认识能够且应该用于癌症的设计和治疗。在本文中,我们从进化的角度对靶向治疗的耐药性进行了综述。提出了凋亡诱导补偿性增殖(AICP)的概念。结果表明,AICP有助于解释在癌症实验中观察到的一些现象。最后,根据AICP提出了潜在的药物靶点。