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Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis
BACKGROUND: RPS15A is a ribosome protein that is highly conserved in many organisms from yeast to human. A number of studies implied its role in promoting cancer cell growth. METHODS: Here, we firstly conducted RPS15A gene expression analysis in brain cancer using Oncomine database and found RPS15A...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850639/ https://www.ncbi.nlm.nih.gov/pubmed/27130037 http://dx.doi.org/10.1186/s12957-016-0891-8 |
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author | Zhang, Chen Fu, Jiqiang Xue, Fei Ryu, Bomi Zhang, Ting Zhang, Shuili Sun, Jingyu Xu, Xinxin Shen, Zhaoli Zheng, Longpo Chen, Xianzhen |
author_facet | Zhang, Chen Fu, Jiqiang Xue, Fei Ryu, Bomi Zhang, Ting Zhang, Shuili Sun, Jingyu Xu, Xinxin Shen, Zhaoli Zheng, Longpo Chen, Xianzhen |
author_sort | Zhang, Chen |
collection | PubMed |
description | BACKGROUND: RPS15A is a ribosome protein that is highly conserved in many organisms from yeast to human. A number of studies implied its role in promoting cancer cell growth. METHODS: Here, we firstly conducted RPS15A gene expression analysis in brain cancer using Oncomine database and found RPS15A was remarkably overexpressed in glioblastoma (GBM) compared with that in normal tissues. Then, the expression of RPS15A was specifically silenced in GBM cell line U251 using lentiviral-mediated RNA interference technique. We further investigated the effect of RPS15A knockdown in U251 cells using MTT assay, colony formation test, and flow cytometry analysis. We detected the protein level of Bcl-2 and poly (ADP-ribose) polymerase (PARP) as well as activation of caspase-3. RESULTS: Our results showed that the knockdown of RPS15A could inhibit cancer cell growth and colony formation in vitro, as well as induced cell cycle arrest at G0/G1 phase and cell apoptosis. In addition, Western blot analysis indicated that the knockdown of RPS15A could significantly inhibit bcl-2 and activate caspase-3 and PARP. CONCLUSIONS: Our findings suggest RPS15A may play an important role in the progression of GBM and lentiviral-mediated silencing of RPS15A could be an effective tool in GBM treatment. |
format | Online Article Text |
id | pubmed-4850639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48506392016-04-30 Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis Zhang, Chen Fu, Jiqiang Xue, Fei Ryu, Bomi Zhang, Ting Zhang, Shuili Sun, Jingyu Xu, Xinxin Shen, Zhaoli Zheng, Longpo Chen, Xianzhen World J Surg Oncol Research BACKGROUND: RPS15A is a ribosome protein that is highly conserved in many organisms from yeast to human. A number of studies implied its role in promoting cancer cell growth. METHODS: Here, we firstly conducted RPS15A gene expression analysis in brain cancer using Oncomine database and found RPS15A was remarkably overexpressed in glioblastoma (GBM) compared with that in normal tissues. Then, the expression of RPS15A was specifically silenced in GBM cell line U251 using lentiviral-mediated RNA interference technique. We further investigated the effect of RPS15A knockdown in U251 cells using MTT assay, colony formation test, and flow cytometry analysis. We detected the protein level of Bcl-2 and poly (ADP-ribose) polymerase (PARP) as well as activation of caspase-3. RESULTS: Our results showed that the knockdown of RPS15A could inhibit cancer cell growth and colony formation in vitro, as well as induced cell cycle arrest at G0/G1 phase and cell apoptosis. In addition, Western blot analysis indicated that the knockdown of RPS15A could significantly inhibit bcl-2 and activate caspase-3 and PARP. CONCLUSIONS: Our findings suggest RPS15A may play an important role in the progression of GBM and lentiviral-mediated silencing of RPS15A could be an effective tool in GBM treatment. BioMed Central 2016-04-29 /pmc/articles/PMC4850639/ /pubmed/27130037 http://dx.doi.org/10.1186/s12957-016-0891-8 Text en © Zhang et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Zhang, Chen Fu, Jiqiang Xue, Fei Ryu, Bomi Zhang, Ting Zhang, Shuili Sun, Jingyu Xu, Xinxin Shen, Zhaoli Zheng, Longpo Chen, Xianzhen Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis |
title | Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis |
title_full | Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis |
title_fullStr | Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis |
title_full_unstemmed | Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis |
title_short | Knockdown of ribosomal protein S15A induces human glioblastoma cell apoptosis |
title_sort | knockdown of ribosomal protein s15a induces human glioblastoma cell apoptosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850639/ https://www.ncbi.nlm.nih.gov/pubmed/27130037 http://dx.doi.org/10.1186/s12957-016-0891-8 |
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