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Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma

机译:抵抗是徒劳的:克服对肺腺癌靶向疗法的抵抗

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摘要

The advent of genomics has led to the identification of specific “driver” mutations in oncogenic kinases, and the development of targeted small molecule inhibitors to block their tumor-driving functions. These specific inhibitors have been a clinical success, and often significantly prolong the lives of individuals with cancer. Inevitably, however, the treated tumors recur as resistance to these targeted therapies develops. Here, we review the major mechanisms by which a cancer cell can evade targeted therapy, focusing on mechanisms of resistance to kinase inhibitors in lung cancer. We discuss the promising concept of rational upfront polytherapy in lung cancer, which involves concurrently targeting multiple proteins in critical signaling pathways in a cancer cell to prevent or delay resistance.
机译:基因组学的出现导致致癌激酶中特定的“驱动”突变的鉴定,以及靶向小分子抑制剂的发展以阻断其肿瘤驱动功能。这些特异性抑制剂已经在临床上取得成功,并且通常显着延长了癌症个体的寿命。然而,不可避免地,随着对这些靶向疗法的耐药性的发展,治疗的肿瘤会复发。在这里,我们回顾了癌细胞可以逃避靶向治疗的主要机制,重点是对肺癌激酶抑制剂的耐药机制。我们讨论了肺癌中合理的前期多联疗法的有希望的概念,它涉及同时靶向癌细胞关键信号通路中的多种蛋白质以预防或延迟耐药性。

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