Format

Send to

Choose Destination
Nat Med. 2013 Nov;19(11):1401-9. doi: 10.1038/nm.3392.

Tumor adaptation and resistance to RAF inhibitors.

Author information

1
1] Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA. [2] Program in Molecular Pharmacology, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.

Abstract

RAF kinase inhibitors have substantial therapeutic effects in patients with BRAF-mutant melanoma. However, only rarely do tumors regress completely, and the therapeutic effects are often temporary. Several mechanisms of resistance to RAF inhibitors have been proposed. The majority of these cause ERK signaling to become insensitive to treatment with RAF inhibitors by increasing the amount of RAF dimers in cells, whereas others bypass the dependence of the tumor on mutant RAF. One motivation for studying mechanisms of drug resistance is that such efforts may suggest new therapeutic targets or rational combination strategies that delay or prevent the emergence of drug-resistant clones. Here, we review the current model of RAF inhibitor resistance with a focus on the implications of this model on ongoing laboratory and clinical efforts to develop more effective therapeutic strategies for patients with BRAF-mutant tumors.

PMID:
24202393
DOI:
10.1038/nm.3392
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Nature Publishing Group
Loading ...
Support Center