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TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer

There is substantial research on the oncogenic role of tripartite motif containing 37 (TRIM37); however, its importance in colorectal cancer (CRC) remains to be elucidated. The present study used reverse transcription-quantitative polymerase chain reaction, immunohistochemistry and western blotting...

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Detalles Bibliográficos
Autores principales: Hu, Cheng-En, Gan, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367363/
https://www.ncbi.nlm.nih.gov/pubmed/28098873
http://dx.doi.org/10.3892/mmr.2017.6125
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author Hu, Cheng-En
Gan, Jun
author_facet Hu, Cheng-En
Gan, Jun
author_sort Hu, Cheng-En
collection PubMed
description There is substantial research on the oncogenic role of tripartite motif containing 37 (TRIM37); however, its importance in colorectal cancer (CRC) remains to be elucidated. The present study used reverse transcription-quantitative polymerase chain reaction, immunohistochemistry and western blotting to detect the expression level of TRIM37 in CRC. The importance of TRIM37 in cell proliferation, invasion and metastasis of CRC were investigated through overexpressing or knocking-down of TRIM37 in CRC cell lines, to observe its function. The present study revealed that TRIM37 was overexpressed in human CRC tissues. High TRIM37 expression resulted in increased CRC proliferation, migration and invasion. Mechanistically, it was confirmed that TRIM37 enhanced invasion and metastasis of CRC via the epithelial-mesenchymal transition pathway. In conclusion, the present study suggested that TRIM3 may contribute to CRC and act as a potential therapeutic target for CRC treatment.
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spelling pubmed-53673632017-04-13 TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer Hu, Cheng-En Gan, Jun Mol Med Rep Articles There is substantial research on the oncogenic role of tripartite motif containing 37 (TRIM37); however, its importance in colorectal cancer (CRC) remains to be elucidated. The present study used reverse transcription-quantitative polymerase chain reaction, immunohistochemistry and western blotting to detect the expression level of TRIM37 in CRC. The importance of TRIM37 in cell proliferation, invasion and metastasis of CRC were investigated through overexpressing or knocking-down of TRIM37 in CRC cell lines, to observe its function. The present study revealed that TRIM37 was overexpressed in human CRC tissues. High TRIM37 expression resulted in increased CRC proliferation, migration and invasion. Mechanistically, it was confirmed that TRIM37 enhanced invasion and metastasis of CRC via the epithelial-mesenchymal transition pathway. In conclusion, the present study suggested that TRIM3 may contribute to CRC and act as a potential therapeutic target for CRC treatment. D.A. Spandidos 2017-03 2017-01-16 /pmc/articles/PMC5367363/ /pubmed/28098873 http://dx.doi.org/10.3892/mmr.2017.6125 Text en Copyright: © Hu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Hu, Cheng-En
Gan, Jun
TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer
title TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer
title_full TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer
title_fullStr TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer
title_full_unstemmed TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer
title_short TRIM37 promotes epithelial-mesenchymal transition in colorectal cancer
title_sort trim37 promotes epithelial-mesenchymal transition in colorectal cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367363/
https://www.ncbi.nlm.nih.gov/pubmed/28098873
http://dx.doi.org/10.3892/mmr.2017.6125
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