MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and Invasion

Differential regulation of gene transcription contributes to cancer metastasis. We investigated the involvement of a Rho GTPase (RhoJ) in breast cancer metastasis focusing on the mechanism underlying RhoJ trans-activation by pro-metastatic cues. We report that expression of RhoJ was up-regulated in...

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Main Authors: Baoyu Chen, Yibiao Yuan, Lina Sun, Junliang Chen, Mengzhu Yang, Yongmei Yin, Yong Xu
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-08-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fcell.2020.00832/full
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spelling doaj-5c3e8341f93f45af82c148984fd55ee92020-11-25T03:40:08ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2020-08-01810.3389/fcell.2020.00832531134MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and InvasionBaoyu Chen0Yibiao Yuan1Lina Sun2Lina Sun3Junliang Chen4Mengzhu Yang5Yongmei Yin6Yong Xu7Yong Xu8Key Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysioloy and Laboratory Center for Experimental Medicine, Nanjing Medical University, Nanjing, ChinaKey Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysioloy and Laboratory Center for Experimental Medicine, Nanjing Medical University, Nanjing, ChinaDepartment of Pathology and Pathophysiology, College of Life and Basic Medical Sciences, Soochow University, Suzhou, ChinaInstitute of Biomedical Research, Liaocheng University, Liaocheng, ChinaDepartment of Pathophysiology, Wuxi Medical School, Jiangnan University, Wuxi, ChinaDepartment of Oncology, First Hospital Affiliated to Nanjing Medical University, Nanjing, ChinaDepartment of Oncology, First Hospital Affiliated to Nanjing Medical University, Nanjing, ChinaKey Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysioloy and Laboratory Center for Experimental Medicine, Nanjing Medical University, Nanjing, ChinaInstitute of Biomedical Research, Liaocheng University, Liaocheng, ChinaDifferential regulation of gene transcription contributes to cancer metastasis. We investigated the involvement of a Rho GTPase (RhoJ) in breast cancer metastasis focusing on the mechanism underlying RhoJ trans-activation by pro-metastatic cues. We report that expression of RhoJ was up-regulated in malignant breast cancer cells compared to more benign ones. Higher RhoJ expression was also detected in human breast cancer biopsy specimens of advanced stages. RhoJ depletion attenuated breast cancer cell migration and invasion in vitro and metastasis in vivo. The pro-metastatic stimulus TGF-β activated RhoJ via megakaryocytic leukemia 1 (MKL1). MKL1 interacted with and was recruited by ETS-related gene 1 (ERG1) to the RhoJ promoter to activate transcription. In conclusion, our data delineate a novel transcriptional pathway that contributes to breast cancer metastasis. Targeting the ERG1-MKL1-RhoJ axis may be considered as a reasonable approach to treat malignant breast cancer.https://www.frontiersin.org/article/10.3389/fcell.2020.00832/fulltranscriptional regulationtranscription factorsbreast cancer metastasisRhoJMKL1ERG1
collection DOAJ
language English
format Article
sources DOAJ
author Baoyu Chen
Yibiao Yuan
Lina Sun
Lina Sun
Junliang Chen
Mengzhu Yang
Yongmei Yin
Yong Xu
Yong Xu
spellingShingle Baoyu Chen
Yibiao Yuan
Lina Sun
Lina Sun
Junliang Chen
Mengzhu Yang
Yongmei Yin
Yong Xu
Yong Xu
MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and Invasion
Frontiers in Cell and Developmental Biology
transcriptional regulation
transcription factors
breast cancer metastasis
RhoJ
MKL1
ERG1
author_facet Baoyu Chen
Yibiao Yuan
Lina Sun
Lina Sun
Junliang Chen
Mengzhu Yang
Yongmei Yin
Yong Xu
Yong Xu
author_sort Baoyu Chen
title MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and Invasion
title_short MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and Invasion
title_full MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and Invasion
title_fullStr MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and Invasion
title_full_unstemmed MKL1 Mediates TGF-β Induced RhoJ Transcription to Promote Breast Cancer Cell Migration and Invasion
title_sort mkl1 mediates tgf-β induced rhoj transcription to promote breast cancer cell migration and invasion
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2020-08-01
description Differential regulation of gene transcription contributes to cancer metastasis. We investigated the involvement of a Rho GTPase (RhoJ) in breast cancer metastasis focusing on the mechanism underlying RhoJ trans-activation by pro-metastatic cues. We report that expression of RhoJ was up-regulated in malignant breast cancer cells compared to more benign ones. Higher RhoJ expression was also detected in human breast cancer biopsy specimens of advanced stages. RhoJ depletion attenuated breast cancer cell migration and invasion in vitro and metastasis in vivo. The pro-metastatic stimulus TGF-β activated RhoJ via megakaryocytic leukemia 1 (MKL1). MKL1 interacted with and was recruited by ETS-related gene 1 (ERG1) to the RhoJ promoter to activate transcription. In conclusion, our data delineate a novel transcriptional pathway that contributes to breast cancer metastasis. Targeting the ERG1-MKL1-RhoJ axis may be considered as a reasonable approach to treat malignant breast cancer.
topic transcriptional regulation
transcription factors
breast cancer metastasis
RhoJ
MKL1
ERG1
url https://www.frontiersin.org/article/10.3389/fcell.2020.00832/full
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