Hallmarks of Anaplastic Lymphoma Kinase Inhibitors with Its Quick Emergence of Drug Resistance

Yong-Fu Qiu, L. Song, Gang-Long Jiang, Zhen Zhang, Xu-Yan Liu, Guan Wang
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Abstract

Anaplastic lymphoma kinase (ALK) is one of the most popular targets for anticancer therapies. In the past decade, the use of anaplastic lymphoma tyrosine kinase inhibitors (ALK-TKIs), including crizotinib and ceritinib, has been a reliable and standard options for patients with lung cancer, particularly for patients with nonsmall cell lung carcinoma. ALK-targeted therapies initially benefit the patients, yet, resistance eventually occurs. Therefore, resistance mechanisms of ALK-TKIs and the solutions have become a formidable challenge in the development of ALK inhibitors. In this review, based on the knowledge of reported ALK inhibitors, we illustrated the crystal structures of ALK, summarized the resistance mechanisms of ALK-targeted drugs, and proposed potential therapeutic strategies to prevent or overcome the resistance.
间变性淋巴瘤激酶抑制剂快速出现耐药性的特点
间变性淋巴瘤激酶(ALK)是抗癌治疗中最受欢迎的靶点之一。在过去的十年中,间变性淋巴瘤酪氨酸激酶抑制剂(ALK-TKIs)的使用,包括克里唑替尼和塞瑞替尼,已经成为肺癌患者,特别是非小细胞肺癌患者的可靠和标准选择。alk靶向治疗最初对患者有益,但最终会出现耐药性。因此,ALK- tkis的耐药机制及其解决方案已成为ALK抑制剂开发中的一个巨大挑战。本文基于对ALK抑制剂的了解,阐述了ALK的晶体结构,总结了ALK靶向药物的耐药机制,并提出了预防或克服ALK耐药的潜在治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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