Mechanisms of Resistance to RAF Inhibitors in Melanoma

被引:66
作者
Aplin, Andrew E. [1 ,2 ]
Kaplan, Fred M.
Shao, Yongping
机构
[1] Thomas Jefferson Univ, Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Dermatol & Cutaneous Surg, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
ACQUIRED-RESISTANCE; BRAF INHIBITION; ERK ACTIVITY; CYCLIN D1; CANCER; CELLS; MUTATIONS; MEK; THERAPY; PATHWAY;
D O I
10.1038/jid.2011.147
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The recent RAF inhibitor trial with PLX4032/RG7204 in late-stage mutant B-RAF melanoma patients has been lauded as a success story for personalized cancer therapy since short-term clinical responses were observed in the majority of patients. However, initial responses were followed by subsequent tumor re-growth, and a subset of patients showed intrinsic resistance. Bi-directional translational efforts are now essential to determine the mechanisms underlying acquired/secondary and intrinsic resistance to RAF inhibitors.
引用
收藏
页码:1817 / 1820
页数:4
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