| Literature DB >> 26605311 |
Niki Karachaliou1, Sara Pilotto1, Cristina Teixidó1, Santiago Viteri1, María González-Cao1, Aldo Riso1, Daniela Morales-Espinosa1, Miguel Angel Molina1, Imane Chaib1, Mariacarmela Santarpia1, Eduardo Richardet1, Emilio Bria1, Rafael Rosell1.
Abstract
Advances and in-depth understanding of the biology of melanoma over the past 30 years have contributed to a change in the consideration of melanoma as one of the most therapy-resistant malignancies. The finding that oncogenic BRAF mutations drive tumor growth in up to 50% of melanomas led to a molecular therapy revolution for unresectable and metastatic disease. Moving beyond BRAF, inactivation of immune regulatory checkpoints that limit T cell responses to melanoma has provided targets for cancer immunotherapy. In this review, we discuss the molecular biology of melanoma and we focus on the recent advances of molecularly targeted and immunotherapeutic approaches.Entities:
Keywords: BRAF; Melanoma; biology; immune system; resistance; targeted therapies
Year: 2015 PMID: 26605311 PMCID: PMC4630557 DOI: 10.3978/j.issn.2305-5839.2015.08.06
Source DB: PubMed Journal: Ann Transl Med ISSN: 2305-5839