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Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance
Cancer Susceptibility Candidate 9 (CASC9) is a novel gene generating long non-coding RNA (lncRNA) with oncogenic potential that was first identified in esophageal cancer. In this study, we have found that CASC9 was overexpressed in gastric cancer (GC) compared to normal gastric tissue. A higher expr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362493/ https://www.ncbi.nlm.nih.gov/pubmed/28146436 http://dx.doi.org/10.18632/oncotarget.14871 |
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author | Shang, Chao Sun, Lin Zhang, Jiale Zhao, Bochao Chen, Xiuxiu Xu, Huimian Huang, Baojun |
author_facet | Shang, Chao Sun, Lin Zhang, Jiale Zhao, Bochao Chen, Xiuxiu Xu, Huimian Huang, Baojun |
author_sort | Shang, Chao |
collection | PubMed |
description | Cancer Susceptibility Candidate 9 (CASC9) is a novel gene generating long non-coding RNA (lncRNA) with oncogenic potential that was first identified in esophageal cancer. In this study, we have found that CASC9 was overexpressed in gastric cancer (GC) compared to normal gastric tissue. A higher expression level was associated with aggressive pathological characteristics, including deep invasion, poor differentiation and lymph node metastases. In two gastric cancer cell lines, BGC823 and SGC7901, CASC9 were both overexpressed compared to that of normal gastric epithelial cell (GES-1). Moreover, the expression of CASC9 was even higher in BGC823/DR and SGC7901/DR cells that are resistant to paclitaxel or adriamycin. CASC9 knockdown inhibited proliferation and promoted cell apoptosis In BGC823/DR and SGC7901/DR cells. The invasion potential was also significantly inhibited measured by Transwell assay. In addition, CASC9 knockdown in BGC823/DR and SGC7901/DR cells restored chemosensitivity to paclitaxel and adriamycin. This was associated with decreased expression of multidrug resistance 1 (MDR1) protein. Taken together, our data suggest that expression of lncRNA CASC9 correlated with aggressive pathological characteristics of GC, it may serve as a potential oncogene to regulate proliferation, invasion, and chemoresistance of GC cells. |
format | Online Article Text |
id | pubmed-5362493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53624932017-04-24 Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance Shang, Chao Sun, Lin Zhang, Jiale Zhao, Bochao Chen, Xiuxiu Xu, Huimian Huang, Baojun Oncotarget Research Paper Cancer Susceptibility Candidate 9 (CASC9) is a novel gene generating long non-coding RNA (lncRNA) with oncogenic potential that was first identified in esophageal cancer. In this study, we have found that CASC9 was overexpressed in gastric cancer (GC) compared to normal gastric tissue. A higher expression level was associated with aggressive pathological characteristics, including deep invasion, poor differentiation and lymph node metastases. In two gastric cancer cell lines, BGC823 and SGC7901, CASC9 were both overexpressed compared to that of normal gastric epithelial cell (GES-1). Moreover, the expression of CASC9 was even higher in BGC823/DR and SGC7901/DR cells that are resistant to paclitaxel or adriamycin. CASC9 knockdown inhibited proliferation and promoted cell apoptosis In BGC823/DR and SGC7901/DR cells. The invasion potential was also significantly inhibited measured by Transwell assay. In addition, CASC9 knockdown in BGC823/DR and SGC7901/DR cells restored chemosensitivity to paclitaxel and adriamycin. This was associated with decreased expression of multidrug resistance 1 (MDR1) protein. Taken together, our data suggest that expression of lncRNA CASC9 correlated with aggressive pathological characteristics of GC, it may serve as a potential oncogene to regulate proliferation, invasion, and chemoresistance of GC cells. Impact Journals LLC 2017-01-27 /pmc/articles/PMC5362493/ /pubmed/28146436 http://dx.doi.org/10.18632/oncotarget.14871 Text en Copyright: © 2017 Shang et al. https://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 Shang, Chao Sun, Lin Zhang, Jiale Zhao, Bochao Chen, Xiuxiu Xu, Huimian Huang, Baojun Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance |
title | Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance |
title_full | Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance |
title_fullStr | Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance |
title_full_unstemmed | Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance |
title_short | Silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance |
title_sort | silence of cancer susceptibility candidate 9 inhibits gastric cancer and reverses chemoresistance |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362493/ https://www.ncbi.nlm.nih.gov/pubmed/28146436 http://dx.doi.org/10.18632/oncotarget.14871 |
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