Potential Therapeutic Strategies to Overcome Acquired Resistance to BRAF or MEK Inhibitors in BRAF Mutant Cancers
Year: 2011
Type: article
Abstract: Ryan B. Corcoran 1,2 , Jeffrey Settleman 3 , Jeffrey A. Engelman 1,2 1 Massachusetts General Hospital Cancer Center, Boston, MA 02129, USA 2 Department of Medicine, Harvard Medical School, Boston, MA 02115, USA 3 Genentech, South San Francisco, CA 94080, USA Keywords: BRAF, MEK; acquired resistance, melanoma, colorectal cancer, NRAS, IGF1R, PDGFR Received: April 15, 2011; Accepted: April 18, 2011; Published: April 19, 2011; Correspondence: Jeffrey A. Engelman, e-mail: // // Abstract Recent clinical trials with selective inhibitors of the BRAF and MEK kinases have shown promising results in patients with tumors harboring BRAF V600 mutations. However, as has been observed previously with similarly successful targeted therapies, acquired resistance to these agents is an emerging problem that limits their clinical benefit. Several recent studies from our laboratory and others have investigated the causes of acquired resistance to BRAF and MEK inhibitors, and multiple resistance mechanisms have been identified. Here, we review these mechanisms and suggest that they can be broadly grouped into two main classes: ERK-dependent and ERK-independent. We also propose distinct therapeutic strategies that might be employed to overcome each class of acquired resistance.
Source: Oncotarget
Institutions: Harvard University, Massachusetts General Hospital, Genentech
Language: English
Topic: Melanoma and MAPK Pathways
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
OpenAlex ID: W1864827749