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MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer
Insulin-like growth factor 1 receptor (IGF1R) is a transmembrane receptor that is activated by insulin-like growth factor 1 (IGF-1) and by a related hormone called IGF-2. It belongs to the large class of tyrosine kinase receptors and plays an important role in colorectal cancer etiology and progress...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256231/ https://www.ncbi.nlm.nih.gov/pubmed/25474488 http://dx.doi.org/10.1371/journal.pone.0114420 |
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author | Su, Jiaojiao Liang, Hongwei Yao, Weiyan Wang, Nan Zhang, Suyang Yan, Xin Feng, Hui Pang, Wenjing Wang, Yanbo Wang, Xueliang Fu, Zhen Liu, Yanqing Zhao, Chihao Zhang, Junfeng Zhang, Chen-Yu Zen, Ke Chen, Xi Wang, Yalei |
author_facet | Su, Jiaojiao Liang, Hongwei Yao, Weiyan Wang, Nan Zhang, Suyang Yan, Xin Feng, Hui Pang, Wenjing Wang, Yanbo Wang, Xueliang Fu, Zhen Liu, Yanqing Zhao, Chihao Zhang, Junfeng Zhang, Chen-Yu Zen, Ke Chen, Xi Wang, Yalei |
author_sort | Su, Jiaojiao |
collection | PubMed |
description | Insulin-like growth factor 1 receptor (IGF1R) is a transmembrane receptor that is activated by insulin-like growth factor 1 (IGF-1) and by a related hormone called IGF-2. It belongs to the large class of tyrosine kinase receptors and plays an important role in colorectal cancer etiology and progression. In this study, we used bioinformatic analyses to search for miRNAs that potentially target IGF1R. We identified specific target sites for miR-143 and miR-145 (miR-143/145) in the 3′-untranslated region (3′-UTR) of the IGF1R gene. These miRNAs are members of a cluster of miRNAs that have been reported to exhibit tumor suppressor activity. Consistent with the bioinformatic analyses, we identified an inverse correlation between miR-143/145 levels and IGF1R protein levels in colorectal cancer tissues. By overexpressing miR-143/145 in Caco2, HT29 and SW480 colorectal cancer cells, we experimentally validated that miR-143/145 directly recognizes the 3′-UTR of the IGF1R transcript and regulates IGF1R expression. Furthermore, the biological consequences of the targeting of IGF1R by miR-143/145 were examined by cell proliferation assays in vitro. We demonstrated that the repression of IGF1R by miR-143/145 suppressed the proliferation of Caco2 cells. Taken together, our findings provide evidence for a role of the miR-143/145 cluster as a tumor suppressor in colorectal cancer through the inhibition of IGF1R translation. |
format | Online Article Text |
id | pubmed-4256231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42562312014-12-11 MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer Su, Jiaojiao Liang, Hongwei Yao, Weiyan Wang, Nan Zhang, Suyang Yan, Xin Feng, Hui Pang, Wenjing Wang, Yanbo Wang, Xueliang Fu, Zhen Liu, Yanqing Zhao, Chihao Zhang, Junfeng Zhang, Chen-Yu Zen, Ke Chen, Xi Wang, Yalei PLoS One Research Article Insulin-like growth factor 1 receptor (IGF1R) is a transmembrane receptor that is activated by insulin-like growth factor 1 (IGF-1) and by a related hormone called IGF-2. It belongs to the large class of tyrosine kinase receptors and plays an important role in colorectal cancer etiology and progression. In this study, we used bioinformatic analyses to search for miRNAs that potentially target IGF1R. We identified specific target sites for miR-143 and miR-145 (miR-143/145) in the 3′-untranslated region (3′-UTR) of the IGF1R gene. These miRNAs are members of a cluster of miRNAs that have been reported to exhibit tumor suppressor activity. Consistent with the bioinformatic analyses, we identified an inverse correlation between miR-143/145 levels and IGF1R protein levels in colorectal cancer tissues. By overexpressing miR-143/145 in Caco2, HT29 and SW480 colorectal cancer cells, we experimentally validated that miR-143/145 directly recognizes the 3′-UTR of the IGF1R transcript and regulates IGF1R expression. Furthermore, the biological consequences of the targeting of IGF1R by miR-143/145 were examined by cell proliferation assays in vitro. We demonstrated that the repression of IGF1R by miR-143/145 suppressed the proliferation of Caco2 cells. Taken together, our findings provide evidence for a role of the miR-143/145 cluster as a tumor suppressor in colorectal cancer through the inhibition of IGF1R translation. Public Library of Science 2014-12-04 /pmc/articles/PMC4256231/ /pubmed/25474488 http://dx.doi.org/10.1371/journal.pone.0114420 Text en © 2014 Su et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Su, Jiaojiao Liang, Hongwei Yao, Weiyan Wang, Nan Zhang, Suyang Yan, Xin Feng, Hui Pang, Wenjing Wang, Yanbo Wang, Xueliang Fu, Zhen Liu, Yanqing Zhao, Chihao Zhang, Junfeng Zhang, Chen-Yu Zen, Ke Chen, Xi Wang, Yalei MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer |
title | MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer |
title_full | MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer |
title_fullStr | MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer |
title_full_unstemmed | MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer |
title_short | MiR-143 and MiR-145 Regulate IGF1R to Suppress Cell Proliferation in Colorectal Cancer |
title_sort | mir-143 and mir-145 regulate igf1r to suppress cell proliferation in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256231/ https://www.ncbi.nlm.nih.gov/pubmed/25474488 http://dx.doi.org/10.1371/journal.pone.0114420 |
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