RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells

10.18632/oncotarget.4654

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Main Authors:	Brusgard, J.L, Choe, M, Chumsri, S, Renoud, K, MacKerell, A.D, Sudol, M, Passaniti, A
Other Authors:	PHYSIOLOGY
Format:	Article
Published:	2020
Subjects:	epidermal growth factor receptor 2 lapatinib neutralizing antibody transcription factor transcription factor RUNX2 transcription factor TAZ trastuzumab unclassified drug uvomorulin cadherin doxycycline protein binding signal peptide WWTR1 protein, human Article breast cancer breast cancer cell line cancer growth carcinogenicity cell nucleus cellular distribution controlled study drug targeting gene silencing human human cell overall survival protein domain protein expression protein function protein localization protein protein interaction signal transduction 3T3 cell line animal breast tumor drug effects gene expression regulation genetics MCF-7 cell line metabolism mouse multicellular spheroid pathology reverse transcription polymerase chain reaction RNA interference solubility Western blotting Animals Blotting, Western Breast Neoplasms Cadherins Core Binding Factor Alpha 1 Subunit Doxycycline Gene Expression Regulation, Neoplastic Humans Intracellular Signaling Peptides and Proteins MCF-7 Cells Mice NIH 3T3 Cells Protein Binding Receptor, ErbB-2 Reverse Transcriptase Polymerase Chain Reaction RNA Interference Signal Transduction Solubility Spheroids, Cellular Transcription Factors
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/174137
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1741372024-04-04T01:11:44Z RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells Brusgard, J.L Choe, M Chumsri, S Renoud, K MacKerell, A.D Sudol, M Passaniti, A PHYSIOLOGY epidermal growth factor receptor 2 lapatinib neutralizing antibody transcription factor transcription factor RUNX2 transcription factor TAZ trastuzumab unclassified drug uvomorulin cadherin doxycycline epidermal growth factor receptor 2 protein binding signal peptide transcription factor transcription factor RUNX2 WWTR1 protein, human Article breast cancer breast cancer cell line cancer growth carcinogenicity cell nucleus cellular distribution controlled study drug targeting gene silencing human human cell overall survival protein domain protein expression protein function protein localization protein protein interaction signal transduction 3T3 cell line animal breast tumor drug effects gene expression regulation genetics MCF-7 cell line metabolism mouse multicellular spheroid pathology reverse transcription polymerase chain reaction RNA interference solubility Western blotting Animals Blotting, Western Breast Neoplasms Cadherins Core Binding Factor Alpha 1 Subunit Doxycycline Gene Expression Regulation, Neoplastic Humans Intracellular Signaling Peptides and Proteins MCF-7 Cells Mice NIH 3T3 Cells Protein Binding Receptor, ErbB-2 Reverse Transcriptase Polymerase Chain Reaction RNA Interference Signal Transduction Solubility Spheroids, Cellular Transcription Factors 10.18632/oncotarget.4654 Oncotarget 6 29 28132-28150 2020-09-03T10:36:45Z 2020-09-03T10:36:45Z 2015 Article Brusgard, J.L, Choe, M, Chumsri, S, Renoud, K, MacKerell, A.D, Sudol, M, Passaniti, A (2015). RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells. Oncotarget 6 (29) : 28132-28150. ScholarBank@NUS Repository. https://doi.org/10.18632/oncotarget.4654 19492553 https://scholarbank.nus.edu.sg/handle/10635/174137 Unpaywall 20200831
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	epidermal growth factor receptor 2 lapatinib neutralizing antibody transcription factor transcription factor RUNX2 transcription factor TAZ trastuzumab unclassified drug uvomorulin cadherin doxycycline epidermal growth factor receptor 2 protein binding signal peptide transcription factor transcription factor RUNX2 WWTR1 protein, human Article breast cancer breast cancer cell line cancer growth carcinogenicity cell nucleus cellular distribution controlled study drug targeting gene silencing human human cell overall survival protein domain protein expression protein function protein localization protein protein interaction signal transduction 3T3 cell line animal breast tumor drug effects gene expression regulation genetics MCF-7 cell line metabolism mouse multicellular spheroid pathology reverse transcription polymerase chain reaction RNA interference solubility Western blotting Animals Blotting, Western Breast Neoplasms Cadherins Core Binding Factor Alpha 1 Subunit Doxycycline Gene Expression Regulation, Neoplastic Humans Intracellular Signaling Peptides and Proteins MCF-7 Cells Mice NIH 3T3 Cells Protein Binding Receptor, ErbB-2 Reverse Transcriptase Polymerase Chain Reaction RNA Interference Signal Transduction Solubility Spheroids, Cellular Transcription Factors
spellingShingle	epidermal growth factor receptor 2 lapatinib neutralizing antibody transcription factor transcription factor RUNX2 transcription factor TAZ trastuzumab unclassified drug uvomorulin cadherin doxycycline epidermal growth factor receptor 2 protein binding signal peptide transcription factor transcription factor RUNX2 WWTR1 protein, human Article breast cancer breast cancer cell line cancer growth carcinogenicity cell nucleus cellular distribution controlled study drug targeting gene silencing human human cell overall survival protein domain protein expression protein function protein localization protein protein interaction signal transduction 3T3 cell line animal breast tumor drug effects gene expression regulation genetics MCF-7 cell line metabolism mouse multicellular spheroid pathology reverse transcription polymerase chain reaction RNA interference solubility Western blotting Animals Blotting, Western Breast Neoplasms Cadherins Core Binding Factor Alpha 1 Subunit Doxycycline Gene Expression Regulation, Neoplastic Humans Intracellular Signaling Peptides and Proteins MCF-7 Cells Mice NIH 3T3 Cells Protein Binding Receptor, ErbB-2 Reverse Transcriptase Polymerase Chain Reaction RNA Interference Signal Transduction Solubility Spheroids, Cellular Transcription Factors Brusgard, J.L Choe, M Chumsri, S Renoud, K MacKerell, A.D Sudol, M Passaniti, A RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells
description	10.18632/oncotarget.4654
author2	PHYSIOLOGY
author_facet	PHYSIOLOGY Brusgard, J.L Choe, M Chumsri, S Renoud, K MacKerell, A.D Sudol, M Passaniti, A
format	Article
author	Brusgard, J.L Choe, M Chumsri, S Renoud, K MacKerell, A.D Sudol, M Passaniti, A
author_sort	Brusgard, J.L
title	RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells
title_short	RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells
title_full	RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells
title_fullStr	RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells
title_full_unstemmed	RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells
title_sort	runx2 and taz-dependent signaling pathways regulate soluble e-cadherin levels and tumorsphere formation in breast cancer cells
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/174137
_version_	1795374321793761280

RUNX2 and TAZ-dependent signaling pathways regulate soluble E-Cadherin levels and tumorsphere formation in breast cancer cells

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