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Emerging targeted therapies for melanoma treatment (Review)

dc.contributor.authorRusso, Angela
dc.contributor.authorFicili, Bartolomea
dc.contributor.authorCandido, Saverio
dc.contributor.authorPezzino, Franca Maria
dc.contributor.authorGuarneri, Claudio
dc.contributor.authorBiondi, Antonio
dc.contributor.authorTravali, Salvatore
dc.contributor.authorMcCubrey, James A.
dc.contributor.authorSpandidos Demetrios A.
dc.contributor.authorLibra, Massimo
dc.date.accessioned2016-06-16T19:40:40Z
dc.date.available2016-06-16T19:40:40Z
dc.date.issued2014-08
dc.description.abstractCutaneous melanoma is an aggressive cancer with a poor prognosis for patients with advanced disease. The identification of several key molecular pathways implicated in the pathogenesis of melanoma has led to the development of novel therapies for this devastating disease. In melanoma, both the Ras/Raf/MEK/ERK (MAPK) and the PI3K/AKT (AKT) signalling pathways are constitutively activated through multiple mechanisms. Targeting various effectors of these pathways with pharmacologic inhibitors may inhibit melanoma cell growth and angiogenesis. Ongoing clinical trials provide hope to improve progression-free survival of patients with advanced melanoma. This review summarizes the most relevant studies focused on the specific action of these new molecular targeted agents. Mechanisms of resistance to therapy are also discussed.en_US
dc.identifier.citationInternational Journal of Oncology; 45:2 p. 516-524en_US
dc.identifier.doi10.3892/ijo.2014.2481
dc.identifier.issn1019-6439
dc.identifier.pmidpmc4091965en_US
dc.identifier.urihttp://hdl.handle.net/10342/5673
dc.relation.urihttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091965/en_US
dc.subjectmelanomaen_US
dc.subjectMAPK/AKT pathwayen_US
dc.subjecttargeted therapiesen_US
dc.titleEmerging targeted therapies for melanoma treatment (Review)en_US
dc.typeArticleen_US
ecu.journal.issue2en_US
ecu.journal.nameInternational Journal of Oncologyen_US
ecu.journal.pages516-524en_US
ecu.journal.volume45en_US

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