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癌症中对受体酪氨酸激酶抑制的耐药性:分子机制与治疗策略。

Resistance to receptor tyrosine kinase inhibition in cancer: molecular mechanisms and therapeutic strategies.

作者信息

Alexander Peter B, Wang Xiao-Fan

机构信息

Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, 27710, USA.

出版信息

Front Med. 2015 Jun;9(2):134-8. doi: 10.1007/s11684-015-0396-9. Epub 2015 May 9.

Abstract

Drug resistance is a major factor that limits the efficacy of targeted cancer therapies. In this review, we discuss the main known mechanisms of resistance to receptor tyrosine kinase inhibitors, which are the most prevalent class of targeted therapeutic agent in current clinical use. Here we focus on bypass track resistance, which involves the activation of alternate signaling molecules by tumor cells to bypass inhibition and maintain signaling output, and consider the problems of signaling pathway redundancy and how the activation of different receptor tyrosine kinases translates into intracellular signal transduction in different cancer types. This information is presented in the context of research strategies for the discovery of new targets for pharmacological intervention, with the goal of overcoming resistance in order to improve patient outcomes.

摘要

耐药性是限制癌症靶向治疗疗效的一个主要因素。在本综述中,我们讨论了对受体酪氨酸激酶抑制剂耐药的主要已知机制,这类抑制剂是目前临床使用中最普遍的一类靶向治疗药物。在这里,我们重点关注旁路耐药,即肿瘤细胞激活替代信号分子以绕过抑制并维持信号输出,并探讨信号通路冗余问题以及不同受体酪氨酸激酶的激活如何在不同癌症类型中转化为细胞内信号转导。这些信息是在发现新的药物干预靶点的研究策略背景下呈现的,目的是克服耐药性以改善患者预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffa5/4535791/3bbcb46d16fa/nihms712418f1.jpg

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