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The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value

The recently described oncogene ZNF217 belongs to a chromosomal region that is frequently amplified in human cancers. Recent findings have revealed that alternative mechanisms such as epigenetic regulation also govern the expression of the encoded ZNF217 protein. Newly discovered molecular functions...

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Autores principales: Cohen, Pascale A., Donini, Caterina F., Nguyen, Nhan T., Lincet, Hubert, Vendrell, Julie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747174/
https://www.ncbi.nlm.nih.gov/pubmed/26431164
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author Cohen, Pascale A.
Donini, Caterina F.
Nguyen, Nhan T.
Lincet, Hubert
Vendrell, Julie A.
author_facet Cohen, Pascale A.
Donini, Caterina F.
Nguyen, Nhan T.
Lincet, Hubert
Vendrell, Julie A.
author_sort Cohen, Pascale A.
collection PubMed
description The recently described oncogene ZNF217 belongs to a chromosomal region that is frequently amplified in human cancers. Recent findings have revealed that alternative mechanisms such as epigenetic regulation also govern the expression of the encoded ZNF217 protein. Newly discovered molecular functions of ZNF217 indicate that it orchestrates complex intracellular circuits as a new key regulator of tumorigenesis. In this review, we focus on recent research on ZNF217-driven molecular functions in human cancers, revisiting major hallmarks of cancer and highlighting the downstream molecular targets and signaling pathways of ZNF217. We also discuss the exciting translational medicine investigating ZNF217 expression levels as a new powerful biomarker, and ZNF217 as a candidate target for future anti-cancer therapies.
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spelling pubmed-47471742016-03-25 The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value Cohen, Pascale A. Donini, Caterina F. Nguyen, Nhan T. Lincet, Hubert Vendrell, Julie A. Oncotarget Review The recently described oncogene ZNF217 belongs to a chromosomal region that is frequently amplified in human cancers. Recent findings have revealed that alternative mechanisms such as epigenetic regulation also govern the expression of the encoded ZNF217 protein. Newly discovered molecular functions of ZNF217 indicate that it orchestrates complex intracellular circuits as a new key regulator of tumorigenesis. In this review, we focus on recent research on ZNF217-driven molecular functions in human cancers, revisiting major hallmarks of cancer and highlighting the downstream molecular targets and signaling pathways of ZNF217. We also discuss the exciting translational medicine investigating ZNF217 expression levels as a new powerful biomarker, and ZNF217 as a candidate target for future anti-cancer therapies. Impact Journals LLC 2015-09-29 /pmc/articles/PMC4747174/ /pubmed/26431164 Text en Copyright: © 2015 Cohen et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Cohen, Pascale A.
Donini, Caterina F.
Nguyen, Nhan T.
Lincet, Hubert
Vendrell, Julie A.
The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value
title The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value
title_full The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value
title_fullStr The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value
title_full_unstemmed The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value
title_short The dark side of ZNF217, a key regulator of tumorigenesis with powerful biomarker value
title_sort dark side of znf217, a key regulator of tumorigenesis with powerful biomarker value
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747174/
https://www.ncbi.nlm.nih.gov/pubmed/26431164
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