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Survivin: A molecular biomarker in cancer

Survivin, a member of the inhibitor of apoptosis (IAP) protein family that inhibits caspases and blocks cell death, is highly expressed in most cancers and is associated with a poor clinical outcome. Survivin has consistently been identified by molecular profiling analysis to be associated with high...

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Detalles Bibliográficos
Autores principales: Jaiswal, Praveen Kumar, Goel, Apul, Mittal, R.D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510718/
https://www.ncbi.nlm.nih.gov/pubmed/26112839
http://dx.doi.org/10.4103/0971-5916.159250
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author Jaiswal, Praveen Kumar
Goel, Apul
Mittal, R.D.
author_facet Jaiswal, Praveen Kumar
Goel, Apul
Mittal, R.D.
author_sort Jaiswal, Praveen Kumar
collection PubMed
description Survivin, a member of the inhibitor of apoptosis (IAP) protein family that inhibits caspases and blocks cell death, is highly expressed in most cancers and is associated with a poor clinical outcome. Survivin has consistently been identified by molecular profiling analysis to be associated with high tumour grade cancers, different disease survival and recurrence. Polymorphisms in the survivin gene are emerging as powerful tools to study the biology of the disease and have the potential to be used in disease prognosis and diagnosis. The survivin gene polymorphisms have also been reported to influence tumour aggressiveness as well as survival of cancer patients. The differential expression of survivin in cancer cells compared to normal tissues and its role as a nodal protein in a number of cellular pathways make it a high target for different therapeutics. This review discusses the complex circuitry of survivin in human cancers and gene variants of survivin, and highlights novel therapy that targets this important protein.
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spelling pubmed-45107182015-07-30 Survivin: A molecular biomarker in cancer Jaiswal, Praveen Kumar Goel, Apul Mittal, R.D. Indian J Med Res Review Article Survivin, a member of the inhibitor of apoptosis (IAP) protein family that inhibits caspases and blocks cell death, is highly expressed in most cancers and is associated with a poor clinical outcome. Survivin has consistently been identified by molecular profiling analysis to be associated with high tumour grade cancers, different disease survival and recurrence. Polymorphisms in the survivin gene are emerging as powerful tools to study the biology of the disease and have the potential to be used in disease prognosis and diagnosis. The survivin gene polymorphisms have also been reported to influence tumour aggressiveness as well as survival of cancer patients. The differential expression of survivin in cancer cells compared to normal tissues and its role as a nodal protein in a number of cellular pathways make it a high target for different therapeutics. This review discusses the complex circuitry of survivin in human cancers and gene variants of survivin, and highlights novel therapy that targets this important protein. Medknow Publications & Media Pvt Ltd 2015-04 /pmc/articles/PMC4510718/ /pubmed/26112839 http://dx.doi.org/10.4103/0971-5916.159250 Text en Copyright: © Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Jaiswal, Praveen Kumar
Goel, Apul
Mittal, R.D.
Survivin: A molecular biomarker in cancer
title Survivin: A molecular biomarker in cancer
title_full Survivin: A molecular biomarker in cancer
title_fullStr Survivin: A molecular biomarker in cancer
title_full_unstemmed Survivin: A molecular biomarker in cancer
title_short Survivin: A molecular biomarker in cancer
title_sort survivin: a molecular biomarker in cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510718/
https://www.ncbi.nlm.nih.gov/pubmed/26112839
http://dx.doi.org/10.4103/0971-5916.159250
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