Cargando…
Targeted therapies in melanoma: Translational research at its finest
The therapeutic landscape for advanced melanoma has expanded in recent years. This expansion has largely been driven by investigational work in melanoma tumor biology and immunology that has been successfully translated to the clinical setting. Molecular evidence generated through benchside experime...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505740/ https://www.ncbi.nlm.nih.gov/pubmed/26174532 http://dx.doi.org/10.1038/jid.2015.14 |
_version_ | 1782381586950389760 |
---|---|
author | Ho, Allen W. Tsao, Hensin |
author_facet | Ho, Allen W. Tsao, Hensin |
author_sort | Ho, Allen W. |
collection | PubMed |
description | The therapeutic landscape for advanced melanoma has expanded in recent years. This expansion has largely been driven by investigational work in melanoma tumor biology and immunology that has been successfully translated to the clinical setting. Molecular evidence generated through benchside experimentation identified BRAF and MEK as key molecular targets in melanoma. This commentary will highlight this work and provide a rationale for the continued importance of translational work in the field of targeted melanoma therapies. |
format | Online Article Text |
id | pubmed-4505740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
record_format | MEDLINE/PubMed |
spelling | pubmed-45057402016-01-31 Targeted therapies in melanoma: Translational research at its finest Ho, Allen W. Tsao, Hensin J Invest Dermatol Article The therapeutic landscape for advanced melanoma has expanded in recent years. This expansion has largely been driven by investigational work in melanoma tumor biology and immunology that has been successfully translated to the clinical setting. Molecular evidence generated through benchside experimentation identified BRAF and MEK as key molecular targets in melanoma. This commentary will highlight this work and provide a rationale for the continued importance of translational work in the field of targeted melanoma therapies. 2015-08 /pmc/articles/PMC4505740/ /pubmed/26174532 http://dx.doi.org/10.1038/jid.2015.14 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Ho, Allen W. Tsao, Hensin Targeted therapies in melanoma: Translational research at its finest |
title | Targeted therapies in melanoma: Translational research at its finest |
title_full | Targeted therapies in melanoma: Translational research at its finest |
title_fullStr | Targeted therapies in melanoma: Translational research at its finest |
title_full_unstemmed | Targeted therapies in melanoma: Translational research at its finest |
title_short | Targeted therapies in melanoma: Translational research at its finest |
title_sort | targeted therapies in melanoma: translational research at its finest |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505740/ https://www.ncbi.nlm.nih.gov/pubmed/26174532 http://dx.doi.org/10.1038/jid.2015.14 |
work_keys_str_mv | AT hoallenw targetedtherapiesinmelanomatranslationalresearchatitsfinest AT tsaohensin targetedtherapiesinmelanomatranslationalresearchatitsfinest |