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Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma

Ovarian cancer is the fifth leading cause of cancer death in women in North America, and approximately two-thirds of cases of ovarian cancer are of high-grade serous type. The remaining cases are comprised of a mix of different tumor types (e.g., endometrioid, clear cell, mucinous, etc.), with no si...

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Detalles Bibliográficos
Autor principal: Gilks, C. Blake
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804051/
https://www.ncbi.nlm.nih.gov/pubmed/20069115
http://dx.doi.org/10.1155/2010/740968
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author Gilks, C. Blake
author_facet Gilks, C. Blake
author_sort Gilks, C. Blake
collection PubMed
description Ovarian cancer is the fifth leading cause of cancer death in women in North America, and approximately two-thirds of cases of ovarian cancer are of high-grade serous type. The remaining cases are comprised of a mix of different tumor types (e.g., endometrioid, clear cell, mucinous, etc.), with no single tumor type accounting for more than 10% of ovarian cancer cases. These tumor types can be reproducibly diagnosed, and each features distinct underlying molecular events during oncogenesis, with a characteristic natural history and response rate to conventional cytotoxic chemotherapy. In this review the molecular abnormalities present in the more common non-high-grade serous subtypes of ovarian cancer will be presented. Development of targeted therapies for these tumor types will require understanding of the genetic basis of each tumor type, and may lead to subtype-specific therapy.
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spelling pubmed-28040512010-01-12 Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma Gilks, C. Blake J Oncol Review Article Ovarian cancer is the fifth leading cause of cancer death in women in North America, and approximately two-thirds of cases of ovarian cancer are of high-grade serous type. The remaining cases are comprised of a mix of different tumor types (e.g., endometrioid, clear cell, mucinous, etc.), with no single tumor type accounting for more than 10% of ovarian cancer cases. These tumor types can be reproducibly diagnosed, and each features distinct underlying molecular events during oncogenesis, with a characteristic natural history and response rate to conventional cytotoxic chemotherapy. In this review the molecular abnormalities present in the more common non-high-grade serous subtypes of ovarian cancer will be presented. Development of targeted therapies for these tumor types will require understanding of the genetic basis of each tumor type, and may lead to subtype-specific therapy. Hindawi Publishing Corporation 2010 2009-12-30 /pmc/articles/PMC2804051/ /pubmed/20069115 http://dx.doi.org/10.1155/2010/740968 Text en Copyright © 2010 C. Blake Gilks. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gilks, C. Blake
Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma
title Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma
title_full Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma
title_fullStr Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma
title_full_unstemmed Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma
title_short Molecular Abnormalities in Ovarian Cancer Subtypes Other than High-Grade Serous Carcinoma
title_sort molecular abnormalities in ovarian cancer subtypes other than high-grade serous carcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804051/
https://www.ncbi.nlm.nih.gov/pubmed/20069115
http://dx.doi.org/10.1155/2010/740968
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