Publication:
c-KIT signaling as the driving oncogenic event in sub-groups of melanomas

dc.contributor.authorSmalley, Keiran S.M.es
dc.contributor.authorSondak, Vernon K.es
dc.contributor.authorWeber, Jeffrey S.
dc.date.accessioned2013-09-24T11:35:04Z
dc.date.available2013-09-24T11:35:04Z
dc.date.issued2009
dc.description.abstractAs we enter the era of targeted therapy for melanoma, attempts are being made to sub-group tumors on the basis of their driving oncogenic mutations, with the hope of developing truly personalized therapeutic regimens. c-KIT is a receptor tyrosine kinase whose aberrant activation is implicated in the progression of gastrointestinal stromal tumors and some acute myeloid leukemias. The role of c-KIT signaling in melanoma has been controversial; although c-KIT activity is critical to melanocyte development, its expression tends to be lost in most melanomas. Some reports have even shown that the re-expression of c-KIT induces apoptosis in melanoma cell lines. The recent publication of work showing the presence of activating c-KIT mutations in acral and mucosal melanomas, as well as melanomas arising on skin with chronic sun damage, has renewed interest in c-KIT signaling in melanoma. Recent work from our own laboratory has further identified melanomas with constitutive c-KIT signaling activity resulting from c- KIT receptor overexpression. Although the initial clinical trials of the c-KIT inhibitor imatinib mesylate in melanoma were negative, some dramatic responses have been seen in patients with very high c-KIT expression and/or documented activating mutations, fostering the belief that focused studies in patients selected on the basis of c-KIT mutational status will yield more encouraging results. The current review discusses the role of c-KIT signaling in melanoma progression and how this new information can be applied to the targeted therapy of melanoma.es
dc.formatapplication/pdfes
dc.format.extent8es
dc.identifier.issn0213-3911es
dc.identifier.urihttp://hdl.handle.net/10201/36018
dc.languageenges
dc.publisherMurcia : F. Hernándezes
dc.relation.ispartofHistology and histopathologyes
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectInatinibes
dc.subjectOcular melanomaes
dc.subject.other616 - Patología. Medicina clínica. Oncologíaes
dc.titlec-KIT signaling as the driving oncogenic event in sub-groups of melanomases
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
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