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Biomarkers in melanoma
Biomarkers are tumour- or host-related factors that correlate with tumour biological behaviour and patient prognosis. High-throughput analytical techniques—DNA and RNA microarrays—have identified numerous possible biomarkers, but their relevance to melanoma progression, clinical outcome and the sele...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2712589/ https://www.ncbi.nlm.nih.gov/pubmed/19617299 http://dx.doi.org/10.1093/annonc/mdp251 |
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author | Gogas, H. Eggermont, A. M. M. Hauschild, A. Hersey, P. Mohr, P. Schadendorf, D. Spatz, A. Dummer, R. |
author_facet | Gogas, H. Eggermont, A. M. M. Hauschild, A. Hersey, P. Mohr, P. Schadendorf, D. Spatz, A. Dummer, R. |
author_sort | Gogas, H. |
collection | PubMed |
description | Biomarkers are tumour- or host-related factors that correlate with tumour biological behaviour and patient prognosis. High-throughput analytical techniques—DNA and RNA microarrays—have identified numerous possible biomarkers, but their relevance to melanoma progression, clinical outcome and the selection of optimal treatment strategies still needs to be established. The review discusses a possible molecular basis for predictive tissue biomarkers such as melanoma thickness, ulceration and mitotic activity, and provides a list of promising new biomarkers identified from tissue microarrays that needs confirmation by independent, prospectively collected clinical data sets. In addition, common predictive serum biomarkers—lactate dehydrogenase, S100B and melanoma-inhibiting activity—as well as selected investigational serum biomarkers such as TA90IC and YKL-40 are also reviewed. A more accurate, therapeutically predictive classification of human melanomas and selection of patient populations that would profit from therapeutic interventions are among the major challenges expected to be addressed in the future. |
format | Text |
id | pubmed-2712589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27125892009-08-01 Biomarkers in melanoma Gogas, H. Eggermont, A. M. M. Hauschild, A. Hersey, P. Mohr, P. Schadendorf, D. Spatz, A. Dummer, R. Ann Oncol Articles Biomarkers are tumour- or host-related factors that correlate with tumour biological behaviour and patient prognosis. High-throughput analytical techniques—DNA and RNA microarrays—have identified numerous possible biomarkers, but their relevance to melanoma progression, clinical outcome and the selection of optimal treatment strategies still needs to be established. The review discusses a possible molecular basis for predictive tissue biomarkers such as melanoma thickness, ulceration and mitotic activity, and provides a list of promising new biomarkers identified from tissue microarrays that needs confirmation by independent, prospectively collected clinical data sets. In addition, common predictive serum biomarkers—lactate dehydrogenase, S100B and melanoma-inhibiting activity—as well as selected investigational serum biomarkers such as TA90IC and YKL-40 are also reviewed. A more accurate, therapeutically predictive classification of human melanomas and selection of patient populations that would profit from therapeutic interventions are among the major challenges expected to be addressed in the future. Oxford University Press 2009-08 /pmc/articles/PMC2712589/ /pubmed/19617299 http://dx.doi.org/10.1093/annonc/mdp251 Text en © The Author 2009. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. The online version of this article has been published under an open access model. users are entitle to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and the European Society for Medical Oncology are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org |
spellingShingle | Articles Gogas, H. Eggermont, A. M. M. Hauschild, A. Hersey, P. Mohr, P. Schadendorf, D. Spatz, A. Dummer, R. Biomarkers in melanoma |
title | Biomarkers in melanoma |
title_full | Biomarkers in melanoma |
title_fullStr | Biomarkers in melanoma |
title_full_unstemmed | Biomarkers in melanoma |
title_short | Biomarkers in melanoma |
title_sort | biomarkers in melanoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2712589/ https://www.ncbi.nlm.nih.gov/pubmed/19617299 http://dx.doi.org/10.1093/annonc/mdp251 |
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