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si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin
Previous studies have revealed that long noncoding RNAs (lncRNAs) function as crucial regulators in various biological processes, including tumorigenesis. Although the expression of lncRNA TP73-antisense RNA1 (AS1) has been identified in hepatocellular carcinoma and glioma, the biological function o...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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D.A. Spandidos
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096144/ https://www.ncbi.nlm.nih.gov/pubmed/30127981 http://dx.doi.org/10.3892/ol.2018.9107 |
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author | Peng, Jianjun |
author_facet | Peng, Jianjun |
author_sort | Peng, Jianjun |
collection | PubMed |
description | Previous studies have revealed that long noncoding RNAs (lncRNAs) function as crucial regulators in various biological processes, including tumorigenesis. Although the expression of lncRNA TP73-antisense RNA1 (AS1) has been identified in hepatocellular carcinoma and glioma, the biological function of TP73-AS1 in gastric cancer (GC) remains unclear. Thus, the present study employed a comprehensive analysis on the function of lncRNA TP73-AS1 in GC. The aim of the present study was to determine the clinical significance and biological function of TP73-AS1 in human GC tissues and cells. Additionally, the expression of TP73-AS1 was increased in GC tissues and cell lines and increased expression level of TP73-AS1 was associated with poor prognosis in patients with GC. Functional assays revealed that silencing of TP73-AS1 may suppress cell proliferation and enhance the chemotherapeutic response of GC cells to cisplatin through targeting the high mobility group 1/receptor for advanced glycation endproducts signaling pathway. Collectively, the results of the present study demonstrated that TP73-AS1 may be a novel lncRNA for the clinical prognosis of GC and a potential therapeutic target for the treatment of GC. |
format | Online Article Text |
id | pubmed-6096144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-60961442018-08-20 si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin Peng, Jianjun Oncol Lett Articles Previous studies have revealed that long noncoding RNAs (lncRNAs) function as crucial regulators in various biological processes, including tumorigenesis. Although the expression of lncRNA TP73-antisense RNA1 (AS1) has been identified in hepatocellular carcinoma and glioma, the biological function of TP73-AS1 in gastric cancer (GC) remains unclear. Thus, the present study employed a comprehensive analysis on the function of lncRNA TP73-AS1 in GC. The aim of the present study was to determine the clinical significance and biological function of TP73-AS1 in human GC tissues and cells. Additionally, the expression of TP73-AS1 was increased in GC tissues and cell lines and increased expression level of TP73-AS1 was associated with poor prognosis in patients with GC. Functional assays revealed that silencing of TP73-AS1 may suppress cell proliferation and enhance the chemotherapeutic response of GC cells to cisplatin through targeting the high mobility group 1/receptor for advanced glycation endproducts signaling pathway. Collectively, the results of the present study demonstrated that TP73-AS1 may be a novel lncRNA for the clinical prognosis of GC and a potential therapeutic target for the treatment of GC. D.A. Spandidos 2018-09 2018-07-10 /pmc/articles/PMC6096144/ /pubmed/30127981 http://dx.doi.org/10.3892/ol.2018.9107 Text en Copyright: © Peng 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 Peng, Jianjun si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin |
title | si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin |
title_full | si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin |
title_fullStr | si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin |
title_full_unstemmed | si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin |
title_short | si-TP73-AS1 suppressed proliferation and increased the chemotherapeutic response of GC cells to cisplatin |
title_sort | si-tp73-as1 suppressed proliferation and increased the chemotherapeutic response of gc cells to cisplatin |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096144/ https://www.ncbi.nlm.nih.gov/pubmed/30127981 http://dx.doi.org/10.3892/ol.2018.9107 |
work_keys_str_mv | AT pengjianjun sitp73as1suppressedproliferationandincreasedthechemotherapeuticresponseofgccellstocisplatin |