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MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28

Colorectal cancer (CRC) is one of the most common prevalent cancer types worldwide. MicroRNAs (miRNAs or miRs) have been demonstrated to play crucial roles in the development, metastasis and drug resistance of CRC. In the present study, a strikingly elevated expression of miR-552 was determined in C...

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Autores principales: Wang, Jian, Li, Hai, Wang, Yong, Wang, Libin, Yan, Xiurui, Zhang, Dong, Ma, Xiaoqiang, Du, Yong, Liu, Xiaoming, Yang, Yinxue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342546/
https://www.ncbi.nlm.nih.gov/pubmed/27661126
http://dx.doi.org/10.18632/oncotarget.12169
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author Wang, Jian
Li, Hai
Wang, Yong
Wang, Libin
Yan, Xiurui
Zhang, Dong
Ma, Xiaoqiang
Du, Yong
Liu, Xiaoming
Yang, Yinxue
author_facet Wang, Jian
Li, Hai
Wang, Yong
Wang, Libin
Yan, Xiurui
Zhang, Dong
Ma, Xiaoqiang
Du, Yong
Liu, Xiaoming
Yang, Yinxue
author_sort Wang, Jian
collection PubMed
description Colorectal cancer (CRC) is one of the most common prevalent cancer types worldwide. MicroRNAs (miRNAs or miRs) have been demonstrated to play crucial roles in the development, metastasis and drug resistance of CRC. In the present study, a strikingly elevated expression of miR-552 was determined in CRC tumor tissues and cells by a miRNA profiling analysis. Importantly, the gene of A Disintegrin And Metalloprotease (ADAM) family member 28 (ADAM28) was identified as a target of miR-552, which was further validated in terms of genetic dual luciferase report assay. Furthermore, an inhibition of miR-552 in LOVE and LS174T CRC cells by transducing miR-552 inhibitor (antagomiR-552) with a lentiviral vector exhibited an ability to reduce cell proliferation, migration and clonogenicity. Moreover, both LOVO and LS174T cells stably expressing miR-552 inhibitor displayed a decreased ability to develop tumors in a murine xenograft model in vivo. In contrast, a knockdown of ADAM28 by short hairpin RNA could reverse the antagomiR-552-induced inhibition of metastatic features of CRC cells in vitro. These results suggested that miR-552 is an oncomir able to promote CRC metastasis in part through a mechanism of targeting ADAM28, which may be a novel target for CRC treatment and warrants for further investigation.
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spelling pubmed-53425462017-03-24 MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28 Wang, Jian Li, Hai Wang, Yong Wang, Libin Yan, Xiurui Zhang, Dong Ma, Xiaoqiang Du, Yong Liu, Xiaoming Yang, Yinxue Oncotarget Research Paper Colorectal cancer (CRC) is one of the most common prevalent cancer types worldwide. MicroRNAs (miRNAs or miRs) have been demonstrated to play crucial roles in the development, metastasis and drug resistance of CRC. In the present study, a strikingly elevated expression of miR-552 was determined in CRC tumor tissues and cells by a miRNA profiling analysis. Importantly, the gene of A Disintegrin And Metalloprotease (ADAM) family member 28 (ADAM28) was identified as a target of miR-552, which was further validated in terms of genetic dual luciferase report assay. Furthermore, an inhibition of miR-552 in LOVE and LS174T CRC cells by transducing miR-552 inhibitor (antagomiR-552) with a lentiviral vector exhibited an ability to reduce cell proliferation, migration and clonogenicity. Moreover, both LOVO and LS174T cells stably expressing miR-552 inhibitor displayed a decreased ability to develop tumors in a murine xenograft model in vivo. In contrast, a knockdown of ADAM28 by short hairpin RNA could reverse the antagomiR-552-induced inhibition of metastatic features of CRC cells in vitro. These results suggested that miR-552 is an oncomir able to promote CRC metastasis in part through a mechanism of targeting ADAM28, which may be a novel target for CRC treatment and warrants for further investigation. Impact Journals LLC 2016-09-21 /pmc/articles/PMC5342546/ /pubmed/27661126 http://dx.doi.org/10.18632/oncotarget.12169 Text en Copyright: © 2016 Wang et al. http://creativecommons.org/licenses/by/3.0/ 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 credited.
spellingShingle Research Paper
Wang, Jian
Li, Hai
Wang, Yong
Wang, Libin
Yan, Xiurui
Zhang, Dong
Ma, Xiaoqiang
Du, Yong
Liu, Xiaoming
Yang, Yinxue
MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28
title MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28
title_full MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28
title_fullStr MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28
title_full_unstemmed MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28
title_short MicroRNA-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28
title_sort microrna-552 enhances metastatic capacity of colorectal cancer cells by targeting a disintegrin and metalloprotease 28
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342546/
https://www.ncbi.nlm.nih.gov/pubmed/27661126
http://dx.doi.org/10.18632/oncotarget.12169
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