[对BRAF抑制剂的耐药性:来自临床观察的教训]。

Medecine sciences : M/S Pub Date : 2022-06-01 Epub Date: 2022-06-29 DOI:10.1051/medsci/2022083
Cylia Dahmani, Eulalie Corre, Sarah Dandou, Alain Mangé, Ovidiu Radulescu, Peter J Coopman, Pierre Cuq, Romain M Larive
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引用次数: 0

摘要

MAPK/ERK通路是细胞内重要的信号通路。它的解除与肿瘤的转化和发展有关。在各种癌症中发现BRAF的激活突变,为BRAF蛋白激酶抑制剂的治疗开辟了新的途径。根据癌症的类型,这些抑制剂要么由于肿瘤细胞的原发性耐药而显示出不足的疗效,要么由于获得性耐药的发展而显示出短暂的疗效。在这篇综述中,我们回顾了导致BRAF抑制剂发展的发现,并详细介绍了这些抑制剂治疗癌症的分子和细胞耐药机制。了解这些机制对于制定更有效的治疗策略至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Resistance to BRAF inhibitors: A lesson from clinical observations].

The MAPK/ERK pathway is an essential intracellular signaling pathway. Its deregulation is involved in tumor transformation and progression. The discovery of activating mutations of BRAF in various cancers has opened new therapeutic avenues with BRAF protein kinase inhibitors. Depending on the type of cancers, these inhibitors have shown either insufficient efficacy due to primary resistance of tumor cells or transient efficacy due to the development of acquired resistance. In this review, we revisit the discoveries that led to the development of BRAF inhibitors and detail the molecular and cellular mechanisms of resistance in cancers treated with these inhibitors. Understanding these mechanisms is crucial for developing more efficient therapeutic strategies.

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