Cargando…

Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene

Tumor suppressor genes are frequently deleted or mutated in lung cancer. The RNA-binding motif protein 10 (RBM10) gene has the ability to suppress tumor activity, but the role of RBM10 during the development of lung cancer has yet to be elucidated. The current study investigated the expression level...

Descripción completa

Detalles Bibliográficos
Autores principales: Ji, Yunxi, Xie, Sheng, Jiang, Li, Liu, Lijian, Li, Liumei, Luo, Lichuan, Chen, Yan, Zhang, Jianxuan, Yu, Lei, Zhang, Yaozhong, Tang, Nong, Liu, Bugu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649569/
https://www.ncbi.nlm.nih.gov/pubmed/29085465
http://dx.doi.org/10.3892/ol.2017.6765
_version_ 1783272565702131712
author Ji, Yunxi
Xie, Sheng
Jiang, Li
Liu, Lijian
Li, Liumei
Luo, Lichuan
Chen, Yan
Zhang, Jianxuan
Yu, Lei
Zhang, Yaozhong
Tang, Nong
Liu, Bugu
author_facet Ji, Yunxi
Xie, Sheng
Jiang, Li
Liu, Lijian
Li, Liumei
Luo, Lichuan
Chen, Yan
Zhang, Jianxuan
Yu, Lei
Zhang, Yaozhong
Tang, Nong
Liu, Bugu
author_sort Ji, Yunxi
collection PubMed
description Tumor suppressor genes are frequently deleted or mutated in lung cancer. The RNA-binding motif protein 10 (RBM10) gene has the ability to suppress tumor activity, but the role of RBM10 during the development of lung cancer has yet to be elucidated. The current study investigated the expression levels of RBM10 in non-tumor and tumor tissues obtained from patients with adenocarcinoma using reverse transcription-polymerase chain reaction and western blot analysis, and identified a reduction in RBM10 expression in lung tumor tissue. To investigate the in vitro and in vivo function of RBM10, A549 human non-small cell lung cancer cells were transfected with the pcDNA-RBM10 vector. Flow cytometry was used to analyze the levels of apoptosis in the transfected cells. Western blot analysis was used to evaluate the expression of B-cell lymphoma 2 (Bcl-2), cleaved caspase-3, caspase-9 and poly (ADP-ribose) polymerase (PARP) proteins in A549 cells and tissues from the A549 xenograft Bagg Albino coat (BALB/c) nude mice model. RBM10 mRNA levels were significantly decreased in adenocarcinoma cells, but not in the non-tumor tissues. The A549 cells and tumor tissues exhibited significant growth inhibition following transfection with the pcDNA-RBM10 vector, which was determined using a cell proliferation assay. Flow cytometry analysis of cells stained with Annexin V/propidium iodide indicated that the overexpression of RBM10 induced apoptosis in A549 cells. The present study demonstrated that the expression levels of Bcl-2 protein were decreased and the expression levels of cleaved caspase-3, caspase-9 and PARP proteins were significantly increased in the A549 cells and cells from ex vivo tumor tissues that were injected with RBM10 vector-containing Salmonella enterica subspecies enterica serovar typhimurium. Notably, the current study identified that the accumulated and stable overexpression of RBM10 in the xenograft BALB/c nude mice model significantly inhibited the tumor growth rate. These results may provide novel insights into the use of RBM10 for lung cancer diagnosis and therapy.
format Online
Article
Text
id pubmed-5649569
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-56495692017-10-30 Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene Ji, Yunxi Xie, Sheng Jiang, Li Liu, Lijian Li, Liumei Luo, Lichuan Chen, Yan Zhang, Jianxuan Yu, Lei Zhang, Yaozhong Tang, Nong Liu, Bugu Oncol Lett Articles Tumor suppressor genes are frequently deleted or mutated in lung cancer. The RNA-binding motif protein 10 (RBM10) gene has the ability to suppress tumor activity, but the role of RBM10 during the development of lung cancer has yet to be elucidated. The current study investigated the expression levels of RBM10 in non-tumor and tumor tissues obtained from patients with adenocarcinoma using reverse transcription-polymerase chain reaction and western blot analysis, and identified a reduction in RBM10 expression in lung tumor tissue. To investigate the in vitro and in vivo function of RBM10, A549 human non-small cell lung cancer cells were transfected with the pcDNA-RBM10 vector. Flow cytometry was used to analyze the levels of apoptosis in the transfected cells. Western blot analysis was used to evaluate the expression of B-cell lymphoma 2 (Bcl-2), cleaved caspase-3, caspase-9 and poly (ADP-ribose) polymerase (PARP) proteins in A549 cells and tissues from the A549 xenograft Bagg Albino coat (BALB/c) nude mice model. RBM10 mRNA levels were significantly decreased in adenocarcinoma cells, but not in the non-tumor tissues. The A549 cells and tumor tissues exhibited significant growth inhibition following transfection with the pcDNA-RBM10 vector, which was determined using a cell proliferation assay. Flow cytometry analysis of cells stained with Annexin V/propidium iodide indicated that the overexpression of RBM10 induced apoptosis in A549 cells. The present study demonstrated that the expression levels of Bcl-2 protein were decreased and the expression levels of cleaved caspase-3, caspase-9 and PARP proteins were significantly increased in the A549 cells and cells from ex vivo tumor tissues that were injected with RBM10 vector-containing Salmonella enterica subspecies enterica serovar typhimurium. Notably, the current study identified that the accumulated and stable overexpression of RBM10 in the xenograft BALB/c nude mice model significantly inhibited the tumor growth rate. These results may provide novel insights into the use of RBM10 for lung cancer diagnosis and therapy. D.A. Spandidos 2017-10 2017-08-17 /pmc/articles/PMC5649569/ /pubmed/29085465 http://dx.doi.org/10.3892/ol.2017.6765 Text en Copyright: © Ji et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Ji, Yunxi
Xie, Sheng
Jiang, Li
Liu, Lijian
Li, Liumei
Luo, Lichuan
Chen, Yan
Zhang, Jianxuan
Yu, Lei
Zhang, Yaozhong
Tang, Nong
Liu, Bugu
Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene
title Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene
title_full Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene
title_fullStr Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene
title_full_unstemmed Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene
title_short Increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by RBM10, a tumor suppressor gene
title_sort increased cell apoptosis in human lung adenocarcinoma and in vivo tumor growth inhibition by rbm10, a tumor suppressor gene
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5649569/
https://www.ncbi.nlm.nih.gov/pubmed/29085465
http://dx.doi.org/10.3892/ol.2017.6765
work_keys_str_mv AT jiyunxi increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT xiesheng increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT jiangli increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT liulijian increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT liliumei increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT luolichuan increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT chenyan increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT zhangjianxuan increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT yulei increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT zhangyaozhong increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT tangnong increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene
AT liubugu increasedcellapoptosisinhumanlungadenocarcinomaandinvivotumorgrowthinhibitionbyrbm10atumorsuppressorgene