Cargando…

Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer

Cell plasticity regulated by the balance between the mesenchymal to epithelial transition (MET) and the opposite program, EMT, is critical in the metastatic cascade. Several transcription factors (TFs) are known to regulate EMT, though the mechanisms of MET remain unclear. We demonstrate a novel fun...

Descripción completa

Detalles Bibliográficos
Autores principales: Roca, Hernan, Hernandez, James, Weidner, Savannah, McEachin, Richard C., Fuller, David, Sud, Sudha, Schumann, Taibriana, Wilkinson, John E., Zaslavsky, Alexander, Li, Hangwen, Maher, Christopher A., Daignault-Newton, Stephanie, Healy, Patrick N., Pienta, Kenneth J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790720/
https://www.ncbi.nlm.nih.gov/pubmed/24124593
http://dx.doi.org/10.1371/journal.pone.0076773
_version_ 1782286632628518912
author Roca, Hernan
Hernandez, James
Weidner, Savannah
McEachin, Richard C.
Fuller, David
Sud, Sudha
Schumann, Taibriana
Wilkinson, John E.
Zaslavsky, Alexander
Li, Hangwen
Maher, Christopher A.
Daignault-Newton, Stephanie
Healy, Patrick N.
Pienta, Kenneth J.
author_facet Roca, Hernan
Hernandez, James
Weidner, Savannah
McEachin, Richard C.
Fuller, David
Sud, Sudha
Schumann, Taibriana
Wilkinson, John E.
Zaslavsky, Alexander
Li, Hangwen
Maher, Christopher A.
Daignault-Newton, Stephanie
Healy, Patrick N.
Pienta, Kenneth J.
author_sort Roca, Hernan
collection PubMed
description Cell plasticity regulated by the balance between the mesenchymal to epithelial transition (MET) and the opposite program, EMT, is critical in the metastatic cascade. Several transcription factors (TFs) are known to regulate EMT, though the mechanisms of MET remain unclear. We demonstrate a novel function of two TFs, OVOL1 and OVOL2, as critical inducers of MET in human cancers. Our findings indicate that the OVOL-TFs control MET through a regulatory feedback loop with EMT-inducing TF ZEB1, and the regulation of mRNA splicing by inducing Epithelial Splicing Regulatory Protein 1 (ESRP1). Using mouse prostate tumor models we show that expression of OVOL-TFs in mesenchymal prostate cancer cells attenuates their metastatic potential. The role of OVOL-TFs as inducers of MET is further supported by expression analyses in 917 cancer cell lines, suggesting their role as crucial regulators of epithelial-mesenchymal cell plasticity in cancer.
format Online
Article
Text
id pubmed-3790720
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37907202013-10-11 Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer Roca, Hernan Hernandez, James Weidner, Savannah McEachin, Richard C. Fuller, David Sud, Sudha Schumann, Taibriana Wilkinson, John E. Zaslavsky, Alexander Li, Hangwen Maher, Christopher A. Daignault-Newton, Stephanie Healy, Patrick N. Pienta, Kenneth J. PLoS One Research Article Cell plasticity regulated by the balance between the mesenchymal to epithelial transition (MET) and the opposite program, EMT, is critical in the metastatic cascade. Several transcription factors (TFs) are known to regulate EMT, though the mechanisms of MET remain unclear. We demonstrate a novel function of two TFs, OVOL1 and OVOL2, as critical inducers of MET in human cancers. Our findings indicate that the OVOL-TFs control MET through a regulatory feedback loop with EMT-inducing TF ZEB1, and the regulation of mRNA splicing by inducing Epithelial Splicing Regulatory Protein 1 (ESRP1). Using mouse prostate tumor models we show that expression of OVOL-TFs in mesenchymal prostate cancer cells attenuates their metastatic potential. The role of OVOL-TFs as inducers of MET is further supported by expression analyses in 917 cancer cell lines, suggesting their role as crucial regulators of epithelial-mesenchymal cell plasticity in cancer. Public Library of Science 2013-10-04 /pmc/articles/PMC3790720/ /pubmed/24124593 http://dx.doi.org/10.1371/journal.pone.0076773 Text en © 2013 Roca et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Roca, Hernan
Hernandez, James
Weidner, Savannah
McEachin, Richard C.
Fuller, David
Sud, Sudha
Schumann, Taibriana
Wilkinson, John E.
Zaslavsky, Alexander
Li, Hangwen
Maher, Christopher A.
Daignault-Newton, Stephanie
Healy, Patrick N.
Pienta, Kenneth J.
Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer
title Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer
title_full Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer
title_fullStr Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer
title_full_unstemmed Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer
title_short Transcription Factors OVOL1 and OVOL2 Induce the Mesenchymal to Epithelial Transition in Human Cancer
title_sort transcription factors ovol1 and ovol2 induce the mesenchymal to epithelial transition in human cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790720/
https://www.ncbi.nlm.nih.gov/pubmed/24124593
http://dx.doi.org/10.1371/journal.pone.0076773
work_keys_str_mv AT rocahernan transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT hernandezjames transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT weidnersavannah transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT mceachinrichardc transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT fullerdavid transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT sudsudha transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT schumanntaibriana transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT wilkinsonjohne transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT zaslavskyalexander transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT lihangwen transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT maherchristophera transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT daignaultnewtonstephanie transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT healypatrickn transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer
AT pientakennethj transcriptionfactorsovol1andovol2inducethemesenchymaltoepithelialtransitioninhumancancer