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Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways
Ovarian cancer is the most lethal gynecologic malignancy. Despite advances in chemotherapy, the five-year survival rate of advanced ovarian cancer patients with peritoneal metastasis remains around 30%. The most significant prognostic factor is stage, and most patients present at an advanced stage w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472771/ https://www.ncbi.nlm.nih.gov/pubmed/23109879 http://dx.doi.org/10.3390/ijms130911705 |
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author | Nakayama, Kentaro Nakayama, Naomi Katagiri, Hiroshi Miyazaki, Kohji |
author_facet | Nakayama, Kentaro Nakayama, Naomi Katagiri, Hiroshi Miyazaki, Kohji |
author_sort | Nakayama, Kentaro |
collection | PubMed |
description | Ovarian cancer is the most lethal gynecologic malignancy. Despite advances in chemotherapy, the five-year survival rate of advanced ovarian cancer patients with peritoneal metastasis remains around 30%. The most significant prognostic factor is stage, and most patients present at an advanced stage with peritoneal dissemination. There is often no clearly identifiable precursor lesion; therefore, the events leading to metastatic disease are poorly understood. This article reviews metastatic suppressor genes, the epithelial-mesenchymal transition (EMT), and the tumor microenvironment as they relate to ovarian cancer metastasis. Additionally, novel chemotherapeutic agents targeting the metastasis-related biochemical pathways are discussed. |
format | Online Article Text |
id | pubmed-3472771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-34727712012-10-29 Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways Nakayama, Kentaro Nakayama, Naomi Katagiri, Hiroshi Miyazaki, Kohji Int J Mol Sci Review Ovarian cancer is the most lethal gynecologic malignancy. Despite advances in chemotherapy, the five-year survival rate of advanced ovarian cancer patients with peritoneal metastasis remains around 30%. The most significant prognostic factor is stage, and most patients present at an advanced stage with peritoneal dissemination. There is often no clearly identifiable precursor lesion; therefore, the events leading to metastatic disease are poorly understood. This article reviews metastatic suppressor genes, the epithelial-mesenchymal transition (EMT), and the tumor microenvironment as they relate to ovarian cancer metastasis. Additionally, novel chemotherapeutic agents targeting the metastasis-related biochemical pathways are discussed. Molecular Diversity Preservation International (MDPI) 2012-09-18 /pmc/articles/PMC3472771/ /pubmed/23109879 http://dx.doi.org/10.3390/ijms130911705 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. 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 | Review Nakayama, Kentaro Nakayama, Naomi Katagiri, Hiroshi Miyazaki, Kohji Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways |
title | Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways |
title_full | Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways |
title_fullStr | Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways |
title_full_unstemmed | Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways |
title_short | Mechanisms of Ovarian Cancer Metastasis: Biochemical Pathways |
title_sort | mechanisms of ovarian cancer metastasis: biochemical pathways |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472771/ https://www.ncbi.nlm.nih.gov/pubmed/23109879 http://dx.doi.org/10.3390/ijms130911705 |
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