Please use this identifier to cite or link to this item: https://doi.org/10.18632/oncotarget.7333
Title: MRTF/SRF dependent transcriptional regulation of TAZ in breast cancer cells
Authors: Liu, C.-Y
Chan, S.W
Guo, F 
Toloczko, A
Cui, L
Hong, W 
Keywords: messenger RNA
myocardin related transcription factor
neu differentiation factor
serum response factor
transcription factor
transcription factor TAZ
unclassified drug
hemoprotein
HRG-1 protein, human
MKL1 protein, human
serum response factor
SRF protein, human
TAZ protein, human
transactivator protein
transcription factor
tumor marker
Article
breast cancer
cancer cell
cell migration
cell nucleus
controlled study
correlation analysis
human
human cell
protein expression
protein localization
protein targeting
transcription regulation
upregulation
breast tumor
cell motion
cell proliferation
female
gene expression regulation
genetics
metabolism
pathology
signal transduction
transcription initiation
tumor cell culture
Biomarkers, Tumor
Breast Neoplasms
Cell Movement
Cell Proliferation
Female
Gene Expression Regulation, Neoplastic
Hemeproteins
Humans
Serum Response Factor
Signal Transduction
Trans-Activators
Transcription Factors
Transcriptional Activation
Tumor Cells, Cultured
Issue Date: 2016
Publisher: Impact Journals LLC
Citation: Liu, C.-Y, Chan, S.W, Guo, F, Toloczko, A, Cui, L, Hong, W (2016). MRTF/SRF dependent transcriptional regulation of TAZ in breast cancer cells. Oncotarget 7 (12) : 13706-13716. ScholarBank@NUS Repository. https://doi.org/10.18632/oncotarget.7333
Rights: Attribution 4.0 International
Abstract: Dysregulation of Hippo pathway results in activation of transcriptional co-activators YAP/TAZ in breast cancer. Previously, we showed that overexpression of TAZ in breast cancer promotes cell migration, invasion and tumorigenesis. Here, we show that upregulation of TAZ in breast cancers could also be due to dysregulation of TAZ transcription. Heregulin ?1 (HRG1) increases TAZ mRNA level in breast cancer cells. TAZ is a direct target of MRTF/SRF transcriptional factors which are activated by HRG1. Both MRTF/SRF and TAZ are the important downstream effectors enhancing cell migration induced by HRG1. TAZ mRNA level is correlated with nuclear localization of MRTF in breast cancer cells and the mRNA level of MRTF/SRF direct target genes in breast cancers, indicating the correlation between MRTF/SRF activity and TAZ expression. Our results provide new insights into the transcriptional regulation of TAZ and dysregulation mechanism of TAZ in breast cancer, which could be a new therapeutic strategy for breast cancer.
Source Title: Oncotarget
URI: https://scholarbank.nus.edu.sg/handle/10635/182490
ISSN: 1949-2553
DOI: 10.18632/oncotarget.7333
Rights: Attribution 4.0 International
Appears in Collections:Elements
Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_18632_oncotarget_7333.pdf8.44 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons