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Expression of Cancer-Associated Molecules in Malignant Mesothelioma

Malignant mesothelioma (MM) is a malignant tumor derived from mesothelial cells, native cells of the body cavities. Exposure to asbestos is the most strongly established etiologic factor, predominantly for the most common disease form, pleural mesothelioma. The pathogenesis of MM involves the accumu...

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Detalles Bibliográficos
Autor principal: Davidson, Ben
Formato: Texto
Lenguaje:English
Publicado: Libertas Academica 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717840/
https://www.ncbi.nlm.nih.gov/pubmed/19662202
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author Davidson, Ben
author_facet Davidson, Ben
author_sort Davidson, Ben
collection PubMed
description Malignant mesothelioma (MM) is a malignant tumor derived from mesothelial cells, native cells of the body cavities. Exposure to asbestos is the most strongly established etiologic factor, predominantly for the most common disease form, pleural mesothelioma. The pathogenesis of MM involves the accumulation of extensive cytogenetic changes, as well as cancer-related phenotypic alterations that facilitate tumor cell survival, invasion and metastasis. This review presents current knowledge regarding the biological characteristics of this disease that are linked to the so-called hallmarks of cancer. In addition, data suggesting that the anatomic site (solid tumor vs. effusion) affects the expression of metastasis-associated and regulatory molecules in MM are presented. Finally, recent work in which high-throughput methodology has been applied to MM research is reviewed. The data obtained in the reviewed research may aid in defining new prognostic markers and therapeutic targets for this aggressive disease in the future.
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spelling pubmed-27178402009-08-06 Expression of Cancer-Associated Molecules in Malignant Mesothelioma Davidson, Ben Biomark Insights Original Research Malignant mesothelioma (MM) is a malignant tumor derived from mesothelial cells, native cells of the body cavities. Exposure to asbestos is the most strongly established etiologic factor, predominantly for the most common disease form, pleural mesothelioma. The pathogenesis of MM involves the accumulation of extensive cytogenetic changes, as well as cancer-related phenotypic alterations that facilitate tumor cell survival, invasion and metastasis. This review presents current knowledge regarding the biological characteristics of this disease that are linked to the so-called hallmarks of cancer. In addition, data suggesting that the anatomic site (solid tumor vs. effusion) affects the expression of metastasis-associated and regulatory molecules in MM are presented. Finally, recent work in which high-throughput methodology has been applied to MM research is reviewed. The data obtained in the reviewed research may aid in defining new prognostic markers and therapeutic targets for this aggressive disease in the future. Libertas Academica 2007-05-30 /pmc/articles/PMC2717840/ /pubmed/19662202 Text en © 2007 by the authors http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Original Research
Davidson, Ben
Expression of Cancer-Associated Molecules in Malignant Mesothelioma
title Expression of Cancer-Associated Molecules in Malignant Mesothelioma
title_full Expression of Cancer-Associated Molecules in Malignant Mesothelioma
title_fullStr Expression of Cancer-Associated Molecules in Malignant Mesothelioma
title_full_unstemmed Expression of Cancer-Associated Molecules in Malignant Mesothelioma
title_short Expression of Cancer-Associated Molecules in Malignant Mesothelioma
title_sort expression of cancer-associated molecules in malignant mesothelioma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2717840/
https://www.ncbi.nlm.nih.gov/pubmed/19662202
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