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A critical role of mir-199a in the cell biological behaviors of colorectal cancer
BACKGROUND: Colorectal cancer (CRC) is one of the most common cancer and the leading causes of cancer mortality worldwide. The critical role of hypoxia-inducible factor 1α (HIF-1α) and vascular endothelial growth factor (VEGF) are important in the cancer development. METHODS: The purpose of this stu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477497/ https://www.ncbi.nlm.nih.gov/pubmed/26065676 http://dx.doi.org/10.1186/s13000-015-0260-x |
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author | Ye, Hua Pang, Liping Wu, Qiong Zhu, Yuzhen Guo, Cancan Deng, Ying Zheng, Xuebao |
author_facet | Ye, Hua Pang, Liping Wu, Qiong Zhu, Yuzhen Guo, Cancan Deng, Ying Zheng, Xuebao |
author_sort | Ye, Hua |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) is one of the most common cancer and the leading causes of cancer mortality worldwide. The critical role of hypoxia-inducible factor 1α (HIF-1α) and vascular endothelial growth factor (VEGF) are important in the cancer development. METHODS: The purpose of this study was to investigate the association of miR-199a expression in CRC and non-tumor tissues as well as assessed the effect of miR-199a on biological behaviors including cell proliferation, apoptosis, migration and invasion of CRC cells. The expression of miR-199a was distinctly decreased in colorectal cancer tissues compared with non-neoplastic colorectal tissues. RESULTS: In this study, we found that miR-199a down-regulation was associated with the CRC and metastasis incidence. Advanced study showed that miR-199a up-regulation would lead to decreased CRC proliferation, migration and invasion. However, no significant association of miR-199a treatment and apoptosis rate and cell-cycle were detected in this study. The detection for the mechanisms of miR-199a on the development of CRC showed that the anticarcinogenic effect of miR-199a might be produced through HIF-1α/VEGF pathway. CONCLUSION: It was found that miR-199a would reduce the proliferation, migration and invasion. However, overexpression of miR-199a on the apoptosis rate and cell cycles showed no significant results. The potential functionary mechanism of miR-199a might through HIF-1α/VEGF pathway. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/9806714131513041. |
format | Online Article Text |
id | pubmed-4477497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44774972015-06-24 A critical role of mir-199a in the cell biological behaviors of colorectal cancer Ye, Hua Pang, Liping Wu, Qiong Zhu, Yuzhen Guo, Cancan Deng, Ying Zheng, Xuebao Diagn Pathol Research BACKGROUND: Colorectal cancer (CRC) is one of the most common cancer and the leading causes of cancer mortality worldwide. The critical role of hypoxia-inducible factor 1α (HIF-1α) and vascular endothelial growth factor (VEGF) are important in the cancer development. METHODS: The purpose of this study was to investigate the association of miR-199a expression in CRC and non-tumor tissues as well as assessed the effect of miR-199a on biological behaviors including cell proliferation, apoptosis, migration and invasion of CRC cells. The expression of miR-199a was distinctly decreased in colorectal cancer tissues compared with non-neoplastic colorectal tissues. RESULTS: In this study, we found that miR-199a down-regulation was associated with the CRC and metastasis incidence. Advanced study showed that miR-199a up-regulation would lead to decreased CRC proliferation, migration and invasion. However, no significant association of miR-199a treatment and apoptosis rate and cell-cycle were detected in this study. The detection for the mechanisms of miR-199a on the development of CRC showed that the anticarcinogenic effect of miR-199a might be produced through HIF-1α/VEGF pathway. CONCLUSION: It was found that miR-199a would reduce the proliferation, migration and invasion. However, overexpression of miR-199a on the apoptosis rate and cell cycles showed no significant results. The potential functionary mechanism of miR-199a might through HIF-1α/VEGF pathway. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/9806714131513041. BioMed Central 2015-06-12 /pmc/articles/PMC4477497/ /pubmed/26065676 http://dx.doi.org/10.1186/s13000-015-0260-x Text en © Ye et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ye, Hua Pang, Liping Wu, Qiong Zhu, Yuzhen Guo, Cancan Deng, Ying Zheng, Xuebao A critical role of mir-199a in the cell biological behaviors of colorectal cancer |
title | A critical role of mir-199a in the cell biological behaviors of colorectal cancer |
title_full | A critical role of mir-199a in the cell biological behaviors of colorectal cancer |
title_fullStr | A critical role of mir-199a in the cell biological behaviors of colorectal cancer |
title_full_unstemmed | A critical role of mir-199a in the cell biological behaviors of colorectal cancer |
title_short | A critical role of mir-199a in the cell biological behaviors of colorectal cancer |
title_sort | critical role of mir-199a in the cell biological behaviors of colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477497/ https://www.ncbi.nlm.nih.gov/pubmed/26065676 http://dx.doi.org/10.1186/s13000-015-0260-x |
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