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PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression
An increasing amount of evidence indicates that peptidylarginine deiminase isoform 4 (PADI4) plays an important role in tumorigenesis. However, the effects of PADI4 on tumor‐bearing mice are unknown, and no studies have investigated this tumorigenic pathway in an animal model. In the present study,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588094/ https://www.ncbi.nlm.nih.gov/pubmed/30242913 http://dx.doi.org/10.1002/mc.22907 |
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author | Liu, Chunyan Tang, Junyi Li, Chang Pu, Guangbo Yang, Dongxia Chang, Xiaotian |
author_facet | Liu, Chunyan Tang, Junyi Li, Chang Pu, Guangbo Yang, Dongxia Chang, Xiaotian |
author_sort | Liu, Chunyan |
collection | PubMed |
description | An increasing amount of evidence indicates that peptidylarginine deiminase isoform 4 (PADI4) plays an important role in tumorigenesis. However, the effects of PADI4 on tumor‐bearing mice are unknown, and no studies have investigated this tumorigenic pathway in an animal model. In the present study, ECA109 cells originating from esophageal squamous cell carcinoma (ESCC) were transfected with PADI4‐expressing lentivirus and were injected into BALB/c nude mice. Tumor size and weight were significantly increased in the mouse tumors established with PADI4‐overexpressing ECA109 cells. PCR array analysis revealed increased CA9 expression in ECA109 cells transfected with a PADI4‐expressing plasmid, while decreased CA9 expression levels were detected in cells transfected with anti‐PADI4 siRNA. Furthermore, up‐regulation of CA9 expression was detected in mouse tumors established with PADI4‐overexpressing cells. Immunohistochemistry detected the increased expression and co‐localization of PADI4 and CA9 in ESCC tissues compared with adjacent non‐tumor tissues and normal tissue controls. These results were verified using Western blotting. Cell proliferation significantly increased or decreased in ECA109 and EC9706 (another ESCC‐originating cell line) cells transfected with a PADI4‐expressing plasmid or anti‐PADI4 siRNA, respectively. The above findings suggest that increased PADI4 expression in ESCC stimulates tumor growth and up‐regulates CA9 expression, which is known to promote metastatic properties in tumor cells. |
format | Online Article Text |
id | pubmed-6588094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65880942019-07-02 PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression Liu, Chunyan Tang, Junyi Li, Chang Pu, Guangbo Yang, Dongxia Chang, Xiaotian Mol Carcinog Articles An increasing amount of evidence indicates that peptidylarginine deiminase isoform 4 (PADI4) plays an important role in tumorigenesis. However, the effects of PADI4 on tumor‐bearing mice are unknown, and no studies have investigated this tumorigenic pathway in an animal model. In the present study, ECA109 cells originating from esophageal squamous cell carcinoma (ESCC) were transfected with PADI4‐expressing lentivirus and were injected into BALB/c nude mice. Tumor size and weight were significantly increased in the mouse tumors established with PADI4‐overexpressing ECA109 cells. PCR array analysis revealed increased CA9 expression in ECA109 cells transfected with a PADI4‐expressing plasmid, while decreased CA9 expression levels were detected in cells transfected with anti‐PADI4 siRNA. Furthermore, up‐regulation of CA9 expression was detected in mouse tumors established with PADI4‐overexpressing cells. Immunohistochemistry detected the increased expression and co‐localization of PADI4 and CA9 in ESCC tissues compared with adjacent non‐tumor tissues and normal tissue controls. These results were verified using Western blotting. Cell proliferation significantly increased or decreased in ECA109 and EC9706 (another ESCC‐originating cell line) cells transfected with a PADI4‐expressing plasmid or anti‐PADI4 siRNA, respectively. The above findings suggest that increased PADI4 expression in ESCC stimulates tumor growth and up‐regulates CA9 expression, which is known to promote metastatic properties in tumor cells. John Wiley and Sons Inc. 2018-10-21 2019-01 /pmc/articles/PMC6588094/ /pubmed/30242913 http://dx.doi.org/10.1002/mc.22907 Text en © 2018 The Authors. Molecular Carcinogenesis Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Articles Liu, Chunyan Tang, Junyi Li, Chang Pu, Guangbo Yang, Dongxia Chang, Xiaotian PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression |
title | PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression |
title_full | PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression |
title_fullStr | PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression |
title_full_unstemmed | PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression |
title_short | PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates CA9 expression |
title_sort | padi4 stimulates esophageal squamous cell carcinoma tumor growth and up‐regulates ca9 expression |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588094/ https://www.ncbi.nlm.nih.gov/pubmed/30242913 http://dx.doi.org/10.1002/mc.22907 |
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