Cargando…

The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression

Basal-like breast cancers (BLBCs) are aggressive breast cancers associated with poor survival. Defining the key drivers of BLBC growth will allow identification of molecules for targeted therapy. In this study, we performed a primary screen integrating multiple assays that compare transcription fact...

Descripción completa

Detalles Bibliográficos
Autores principales: Shepherd, Jonathan H., Uray, Ivan P., Mazumdar, Abhijit, Tsimelzon, Anna, Savage, Michelle, Hilsenbeck, Susan G., Brown, Powel H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914345/
https://www.ncbi.nlm.nih.gov/pubmed/26894864
http://dx.doi.org/10.18632/oncotarget.7437
_version_ 1782438548384776192
author Shepherd, Jonathan H.
Uray, Ivan P.
Mazumdar, Abhijit
Tsimelzon, Anna
Savage, Michelle
Hilsenbeck, Susan G.
Brown, Powel H.
author_facet Shepherd, Jonathan H.
Uray, Ivan P.
Mazumdar, Abhijit
Tsimelzon, Anna
Savage, Michelle
Hilsenbeck, Susan G.
Brown, Powel H.
author_sort Shepherd, Jonathan H.
collection PubMed
description Basal-like breast cancers (BLBCs) are aggressive breast cancers associated with poor survival. Defining the key drivers of BLBC growth will allow identification of molecules for targeted therapy. In this study, we performed a primary screen integrating multiple assays that compare transcription factor expression and activity in BLBC and non-BLBC at the RNA, DNA, and protein levels. This integrated screen identified 33 transcription factors that were elevated in BLBC in multiple assays comparing mRNA expression, DNA cis-element sequences, or protein DNA-binding activity. In a secondary screen to identify transcription factors critical for BLBC cell growth, 8 of the 33 candidate transcription factors (TFs) were found to be necessary for growth in at least two of three BLBC cell lines. Of these 8 transcription factors, SOX11 was the only transcription factor required for BLBC growth, but not for growth of non-BLBC cells. Our studies demonstrate that SOX11 is a critical regulator of multiple BLBC phenotypes, including growth, migration, invasion, and expression of signature BLBC genes. High SOX11 expression was also found to be an independent prognostic indicator of poor survival in women with breast cancer. These results identify SOX11 as a potential target for the treatment of BLBC, the most aggressive form of breast cancer.
format Online
Article
Text
id pubmed-4914345
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-49143452016-07-11 The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression Shepherd, Jonathan H. Uray, Ivan P. Mazumdar, Abhijit Tsimelzon, Anna Savage, Michelle Hilsenbeck, Susan G. Brown, Powel H. Oncotarget Research Paper Basal-like breast cancers (BLBCs) are aggressive breast cancers associated with poor survival. Defining the key drivers of BLBC growth will allow identification of molecules for targeted therapy. In this study, we performed a primary screen integrating multiple assays that compare transcription factor expression and activity in BLBC and non-BLBC at the RNA, DNA, and protein levels. This integrated screen identified 33 transcription factors that were elevated in BLBC in multiple assays comparing mRNA expression, DNA cis-element sequences, or protein DNA-binding activity. In a secondary screen to identify transcription factors critical for BLBC cell growth, 8 of the 33 candidate transcription factors (TFs) were found to be necessary for growth in at least two of three BLBC cell lines. Of these 8 transcription factors, SOX11 was the only transcription factor required for BLBC growth, but not for growth of non-BLBC cells. Our studies demonstrate that SOX11 is a critical regulator of multiple BLBC phenotypes, including growth, migration, invasion, and expression of signature BLBC genes. High SOX11 expression was also found to be an independent prognostic indicator of poor survival in women with breast cancer. These results identify SOX11 as a potential target for the treatment of BLBC, the most aggressive form of breast cancer. Impact Journals LLC 2016-02-17 /pmc/articles/PMC4914345/ /pubmed/26894864 http://dx.doi.org/10.18632/oncotarget.7437 Text en Copyright: © 2016 Shepherd 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 Research Paper
Shepherd, Jonathan H.
Uray, Ivan P.
Mazumdar, Abhijit
Tsimelzon, Anna
Savage, Michelle
Hilsenbeck, Susan G.
Brown, Powel H.
The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression
title The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression
title_full The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression
title_fullStr The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression
title_full_unstemmed The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression
title_short The SOX11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression
title_sort sox11 transcription factor is a critical regulator of basal-like breast cancer growth, invasion, and basal-like gene expression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914345/
https://www.ncbi.nlm.nih.gov/pubmed/26894864
http://dx.doi.org/10.18632/oncotarget.7437
work_keys_str_mv AT shepherdjonathanh thesox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT urayivanp thesox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT mazumdarabhijit thesox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT tsimelzonanna thesox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT savagemichelle thesox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT hilsenbecksusang thesox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT brownpowelh thesox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT shepherdjonathanh sox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT urayivanp sox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT mazumdarabhijit sox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT tsimelzonanna sox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT savagemichelle sox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT hilsenbecksusang sox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression
AT brownpowelh sox11transcriptionfactorisacriticalregulatorofbasallikebreastcancergrowthinvasionandbasallikegeneexpression