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Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer

Aims: Activin A receptor type 2A (ACVR2A) is a membrane receptor in the transforming growth factor- beta (TGF-β signaling pathway, which is involved in the regulation of cell proliferation, migration, and apoptosis. The aim of this study was to examine the expression profiles and biological function...

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Autores principales: Zhuo, Changhua, Hu, Dan, Li, Jing, Yu, Hui, Lin, Xiandong, Chen, Ying, Zhuang, Yong, Li, Qingguo, Zheng, Xiongwei, Yang, Chunkang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171025/
https://www.ncbi.nlm.nih.gov/pubmed/30310521
http://dx.doi.org/10.7150/jca.26790
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author Zhuo, Changhua
Hu, Dan
Li, Jing
Yu, Hui
Lin, Xiandong
Chen, Ying
Zhuang, Yong
Li, Qingguo
Zheng, Xiongwei
Yang, Chunkang
author_facet Zhuo, Changhua
Hu, Dan
Li, Jing
Yu, Hui
Lin, Xiandong
Chen, Ying
Zhuang, Yong
Li, Qingguo
Zheng, Xiongwei
Yang, Chunkang
author_sort Zhuo, Changhua
collection PubMed
description Aims: Activin A receptor type 2A (ACVR2A) is a membrane receptor in the transforming growth factor- beta (TGF-β signaling pathway, which is involved in the regulation of cell proliferation, migration, and apoptosis. The aim of this study was to examine the expression profiles and biological functions of ACVR2A in colon cancer. Methods: ACVR2A expression was investigated using the GSE39582 database and two validation cohorts. An in vitro study of cell proliferation and migration of human colon cell lines was also performed. Results: In the GSE39582 database (n= 497), expression of ACVR2A mRNA was identified as a prognostic factor by linear regression analysis. In one validation cohort of 15 patients with stage IV cancer, the mRNA expression of ACVR2A was significantly reduced in metastatic lesions and primary tumors compared with adjacent normal controls (P = 0.001). In another validation cohort of tissue microarray (TMA) consisting of 193 cases, reduced ACVR2A protein expression correlated with advanced N stage (P = 0.001) and positive lymphovascular invasion (P = 0.005). Strong correlations between low ACVR2A mRNA or protein expression and worse survival were also observed in the GSE39582 database and the TMA validation cohort (all P < 0.05). Moreover, our in vitro studies showed a remarkable increase in cell migration in ACVR2A knockdown cells. Conclusions: Our findings indicate that loss of ACVR2A has an important role in cancer progression and distant metastasis and may serve as a prognostic marker in patients with colon cancer.
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spelling pubmed-61710252018-10-11 Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer Zhuo, Changhua Hu, Dan Li, Jing Yu, Hui Lin, Xiandong Chen, Ying Zhuang, Yong Li, Qingguo Zheng, Xiongwei Yang, Chunkang J Cancer Research Paper Aims: Activin A receptor type 2A (ACVR2A) is a membrane receptor in the transforming growth factor- beta (TGF-β signaling pathway, which is involved in the regulation of cell proliferation, migration, and apoptosis. The aim of this study was to examine the expression profiles and biological functions of ACVR2A in colon cancer. Methods: ACVR2A expression was investigated using the GSE39582 database and two validation cohorts. An in vitro study of cell proliferation and migration of human colon cell lines was also performed. Results: In the GSE39582 database (n= 497), expression of ACVR2A mRNA was identified as a prognostic factor by linear regression analysis. In one validation cohort of 15 patients with stage IV cancer, the mRNA expression of ACVR2A was significantly reduced in metastatic lesions and primary tumors compared with adjacent normal controls (P = 0.001). In another validation cohort of tissue microarray (TMA) consisting of 193 cases, reduced ACVR2A protein expression correlated with advanced N stage (P = 0.001) and positive lymphovascular invasion (P = 0.005). Strong correlations between low ACVR2A mRNA or protein expression and worse survival were also observed in the GSE39582 database and the TMA validation cohort (all P < 0.05). Moreover, our in vitro studies showed a remarkable increase in cell migration in ACVR2A knockdown cells. Conclusions: Our findings indicate that loss of ACVR2A has an important role in cancer progression and distant metastasis and may serve as a prognostic marker in patients with colon cancer. Ivyspring International Publisher 2018-09-08 /pmc/articles/PMC6171025/ /pubmed/30310521 http://dx.doi.org/10.7150/jca.26790 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Zhuo, Changhua
Hu, Dan
Li, Jing
Yu, Hui
Lin, Xiandong
Chen, Ying
Zhuang, Yong
Li, Qingguo
Zheng, Xiongwei
Yang, Chunkang
Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer
title Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer
title_full Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer
title_fullStr Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer
title_full_unstemmed Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer
title_short Downregulation of Activin A Receptor Type 2A Is Associated with Metastatic Potential and Poor Prognosis of Colon Cancer
title_sort downregulation of activin a receptor type 2a is associated with metastatic potential and poor prognosis of colon cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171025/
https://www.ncbi.nlm.nih.gov/pubmed/30310521
http://dx.doi.org/10.7150/jca.26790
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