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Narrowing the knowledge gaps for melanoma

Cutaneous melanoma originates from pigment producing melanocytes or their precursors and is considered the deadliest form of skin cancer. For the last 40 years, few treatment options were available for patients with late-stage melanoma. However, remarkable advances in the therapy field were made rec...

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Detalles Bibliográficos
Autores principales: Slipicevic, Ana, Herlyn, Meenhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339555/
https://www.ncbi.nlm.nih.gov/pubmed/22339359
http://dx.doi.org/10.3109/03009734.2012.658977
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author Slipicevic, Ana
Herlyn, Meenhard
author_facet Slipicevic, Ana
Herlyn, Meenhard
author_sort Slipicevic, Ana
collection PubMed
description Cutaneous melanoma originates from pigment producing melanocytes or their precursors and is considered the deadliest form of skin cancer. For the last 40 years, few treatment options were available for patients with late-stage melanoma. However, remarkable advances in the therapy field were made recently, leading to the approval of two new drugs, the mutant BRAF inhibitor vemurafenib and the immunostimulant ipilimumab. Although these drugs prolong patients' lives, neither drug cures the disease completely, emphasizing the need for improvements of current therapies. Our knowledge about the complex genetic and biological mechanisms leading to melanoma development has increased, but there are still gaps in our understanding of the early events of melanocyte transformation and disease progression. In this review, we present a summary of the main contributing factors leading to melanocyte transformation and discuss recent novel findings and technologies that will help answer some of the key biological melanoma questions and lay the groundwork for novel therapies.
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spelling pubmed-33395552012-05-24 Narrowing the knowledge gaps for melanoma Slipicevic, Ana Herlyn, Meenhard Ups J Med Sci Review Article Cutaneous melanoma originates from pigment producing melanocytes or their precursors and is considered the deadliest form of skin cancer. For the last 40 years, few treatment options were available for patients with late-stage melanoma. However, remarkable advances in the therapy field were made recently, leading to the approval of two new drugs, the mutant BRAF inhibitor vemurafenib and the immunostimulant ipilimumab. Although these drugs prolong patients' lives, neither drug cures the disease completely, emphasizing the need for improvements of current therapies. Our knowledge about the complex genetic and biological mechanisms leading to melanoma development has increased, but there are still gaps in our understanding of the early events of melanocyte transformation and disease progression. In this review, we present a summary of the main contributing factors leading to melanocyte transformation and discuss recent novel findings and technologies that will help answer some of the key biological melanoma questions and lay the groundwork for novel therapies. Informa Healthcare 2012-05 2012-04-19 /pmc/articles/PMC3339555/ /pubmed/22339359 http://dx.doi.org/10.3109/03009734.2012.658977 Text en © Informa Healthcare http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.
spellingShingle Review Article
Slipicevic, Ana
Herlyn, Meenhard
Narrowing the knowledge gaps for melanoma
title Narrowing the knowledge gaps for melanoma
title_full Narrowing the knowledge gaps for melanoma
title_fullStr Narrowing the knowledge gaps for melanoma
title_full_unstemmed Narrowing the knowledge gaps for melanoma
title_short Narrowing the knowledge gaps for melanoma
title_sort narrowing the knowledge gaps for melanoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339555/
https://www.ncbi.nlm.nih.gov/pubmed/22339359
http://dx.doi.org/10.3109/03009734.2012.658977
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