Matching wits with melanoma brain metastases: from biology to therapeutics.
Identifieur interne : 002256 ( Main/Exploration ); précédent : 002255; suivant : 002257Matching wits with melanoma brain metastases: from biology to therapeutics.
Auteurs : Hussein Tawbi [États-Unis]Source :
- Clinical cancer research : an official journal of the American Association for Cancer Research [ 1078-0432 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Mélanome, Tumeurs du cerveau.
- génétique : Mélanome, Métastase tumorale, Phosphatidylinositol 3-kinases, Tumeurs du cerveau.
- Humains.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Phosphatidylinositol 3-Kinases.
- genetics : Brain Neoplasms, Melanoma, Neoplasm Metastasis.
- pathology : Brain Neoplasms, Melanoma.
- Humans.
Abstract
Melanoma brain metastases (MBM) present a significant clinical challenge. Molecular profiling of MBM is useful to identify molecular pathways, such as the PI3K pathway, that are specifically and differentially altered in MBM. Therapeutic studies should recruit patients with MBM and prospective tissue collection will lay the foundation for further advances.
DOI: 10.1158/1078-0432.CCR-14-1121
PubMed: 25135484
Affiliations:
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Le document en format XML
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<term>Tumeurs du cerveau</term>
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<term>Métastase tumorale</term>
<term>Phosphatidylinositol 3-kinases</term>
<term>Tumeurs du cerveau</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Brain Neoplasms</term>
<term>Melanoma</term>
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<front><div type="abstract" xml:lang="en">Melanoma brain metastases (MBM) present a significant clinical challenge. Molecular profiling of MBM is useful to identify molecular pathways, such as the PI3K pathway, that are specifically and differentially altered in MBM. Therapeutic studies should recruit patients with MBM and prospective tissue collection will lay the foundation for further advances.</div>
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