Therapeutic Inhibitors against Mutated BRAF and MEK for the Treatment of Metastatic Melanoma

Melanoma is one of the most aggressive cancers in the world and is responsible for the majority of skin cancer deaths. Recent advances in the field of immunotherapy using active, adoptive, and antigen-specific therapeutic approaches, have generated the expectation that these technologies have the po...

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Bibliographic Details
Published in:Chonnam medical journal Vol. 53; no. 3; pp. 173 - 177
Main Authors: Ryu, Sunhyo, Youn, Chakyung, Moon, Ae Ran, Howland, Amanda, Armstrong, Cheryl A, Song, Peter I
Format: Journal Article
Language:English
Published: Korea (South) Chonnam National University Medical School 01-09-2017
의과학연구소
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Summary:Melanoma is one of the most aggressive cancers in the world and is responsible for the majority of skin cancer deaths. Recent advances in the field of immunotherapy using active, adoptive, and antigen-specific therapeutic approaches, have generated the expectation that these technologies have the potential to improve the treatment of advanced malignancies, including melanoma. Treatment options for metastatic melanoma patients have been dramatically improved by the FDA approval of new therapeutic agents including vemurafenib, dabrafenib, and sorafenib. These kinase inhibitors have the potential to work in tandem with MEK, PI3K/AKT, and mTOR to inhibit the activity of melanoma inducing BRAF mutations. This review summarizes the effects of the new therapeutic agents against melanoma and the underlying biology of these BRAF inhibitors.
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ISSN:2233-7385
2233-7393
DOI:10.4068/cmj.2017.53.3.173