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MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer
Gastric cancer (GC) is one of the most common malignancies worldwide. In particular, scirrhous type GC is highly metastatic and is characterized clinically by rapid disease progression and poor prognosis. MicroRNAs (miRNAs) play crucial roles in cancer development and progression. In the present stu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317817/ https://www.ncbi.nlm.nih.gov/pubmed/24283360 http://dx.doi.org/10.1111/cas.12329 |
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author | Naito, Yutaka Sakamoto, Naoya Oue, Naohide Yashiro, Masakazu Sentani, Kazuhiro Yanagihara, Kazuyoshi Hirakawa, Kosei Yasui, Wataru |
author_facet | Naito, Yutaka Sakamoto, Naoya Oue, Naohide Yashiro, Masakazu Sentani, Kazuhiro Yanagihara, Kazuyoshi Hirakawa, Kosei Yasui, Wataru |
author_sort | Naito, Yutaka |
collection | PubMed |
description | Gastric cancer (GC) is one of the most common malignancies worldwide. In particular, scirrhous type GC is highly metastatic and is characterized clinically by rapid disease progression and poor prognosis. MicroRNAs (miRNAs) play crucial roles in cancer development and progression. In the present study, we identified several miRNAs that are expressed at higher levels in scirrhous type GC than in non-scirrhous type GC by miRNA microarray analysis. Among these, microRNA-143 (miR-143) expression was higher in scirrhous type GC than in non-scirrhous types of GC. In situ hybridization and quantitative RT-PCR analysis showed that miR-143 is expressed by stromal fibroblasts but not by cancer cells. In stromal cells, miR-143 enhanced collagen type III expression in normal gastric fibroblasts and cancer-associated fibroblasts through activation of transforming growth factor-β)/SMAD signaling. Furthermore, high miR-143 expression in GC was associated with worse cancer-specific mortality (P = 0.0141). Multivariate analysis revealed that miR-143 was an independent prognostic factor. Treatment of GC cell lines with 5-aza-2′-deoxycytidine restored the expression of miR-143, and precursor miR-143 caused the inhibition of cancer cell invasion. These data suggest that miR-143 regulates fibrosis of scirrhous type GC through induction of collagen expression in stromal fibroblasts and that miR-143 expression serves as a prognostic marker of GC. |
format | Online Article Text |
id | pubmed-4317817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43178172015-10-05 MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer Naito, Yutaka Sakamoto, Naoya Oue, Naohide Yashiro, Masakazu Sentani, Kazuhiro Yanagihara, Kazuyoshi Hirakawa, Kosei Yasui, Wataru Cancer Sci Original Articles Gastric cancer (GC) is one of the most common malignancies worldwide. In particular, scirrhous type GC is highly metastatic and is characterized clinically by rapid disease progression and poor prognosis. MicroRNAs (miRNAs) play crucial roles in cancer development and progression. In the present study, we identified several miRNAs that are expressed at higher levels in scirrhous type GC than in non-scirrhous type GC by miRNA microarray analysis. Among these, microRNA-143 (miR-143) expression was higher in scirrhous type GC than in non-scirrhous types of GC. In situ hybridization and quantitative RT-PCR analysis showed that miR-143 is expressed by stromal fibroblasts but not by cancer cells. In stromal cells, miR-143 enhanced collagen type III expression in normal gastric fibroblasts and cancer-associated fibroblasts through activation of transforming growth factor-β)/SMAD signaling. Furthermore, high miR-143 expression in GC was associated with worse cancer-specific mortality (P = 0.0141). Multivariate analysis revealed that miR-143 was an independent prognostic factor. Treatment of GC cell lines with 5-aza-2′-deoxycytidine restored the expression of miR-143, and precursor miR-143 caused the inhibition of cancer cell invasion. These data suggest that miR-143 regulates fibrosis of scirrhous type GC through induction of collagen expression in stromal fibroblasts and that miR-143 expression serves as a prognostic marker of GC. Blackwell Publishing Ltd 2014-02 2014-01-08 /pmc/articles/PMC4317817/ /pubmed/24283360 http://dx.doi.org/10.1111/cas.12329 Text en © 2013 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is noncommercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Naito, Yutaka Sakamoto, Naoya Oue, Naohide Yashiro, Masakazu Sentani, Kazuhiro Yanagihara, Kazuyoshi Hirakawa, Kosei Yasui, Wataru MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer |
title | MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer |
title_full | MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer |
title_fullStr | MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer |
title_full_unstemmed | MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer |
title_short | MicroRNA-143 regulates collagen type III expression in stromal fibroblasts of scirrhous type gastric cancer |
title_sort | microrna-143 regulates collagen type iii expression in stromal fibroblasts of scirrhous type gastric cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317817/ https://www.ncbi.nlm.nih.gov/pubmed/24283360 http://dx.doi.org/10.1111/cas.12329 |
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