黑色素瘤
抗性(生态学)
后天抵抗
癌症研究
免疫疗法
抗药性
转移性黑色素瘤
MEK抑制剂
MAPK/ERK通路
突变
医学
生物
癌症
激酶
内科学
遗传学
基因
生态学
作者
Qing-Shan Li,Bang-Nian Shen,Hua‐Jian Xu,Ban‐Feng Ruan
出处
期刊:Anti-cancer Agents in Medicinal Chemistry
[Bentham Science]
日期:2020-04-23
卷期号:20 (12): 1415-1430
被引量:4
标识
DOI:10.2174/1871520620666200422073622
摘要
Almost 50% of metastatic melanomas harbor BRAF mutations. Since 2011, BRAF inhibitors have exhibited striking clinical benefits in BRAF-mutant melanoma patients. Unfortunately, their therapeutic effects are often temporary. The resistance mechanisms vary and can be broadly classified as MAPK reactivation-dependent and -independent. Elucidation of these resistance mechanisms provides new insights into strategies for overcoming resistance. Indeed, several alternative treatment strategies, including changes in the mode of administration, combinations of BRAF and MEK inhibitors, and immunotherapy have been verified as beneficial to BRAF inhibitor-resistant melanoma patients.In this review, we discuss promising strategies for overcoming drug resistance and highlighting the prospects for discovering strategies to counteract BRAF inhibitor resistance.
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