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LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas

Anaplastic glioma is Grade III and the median overall survival is about 37.6 months. However, there are still other factors that affect the prognosis for anaplastic glioma patients due to variable overall survival. So we screened four-lncRNA signature (AGAP2-AS1, TPT1-AS1, LINC01198 and MIR155HG) fr...

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Autores principales: Wang, Wen, Yang, Fan, Zhang, Lu, Chen, Jing, Zhao, Zheng, Wang, Haoyuan, Wu, Fan, Liang, Tingyu, Yan, Xiaoyan, Li, Jiye, Lan, Qing, Wang, Jiangfei, Zhao, Jizong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363582/
https://www.ncbi.nlm.nih.gov/pubmed/27764782
http://dx.doi.org/10.18632/oncotarget.12624
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author Wang, Wen
Yang, Fan
Zhang, Lu
Chen, Jing
Zhao, Zheng
Wang, Haoyuan
Wu, Fan
Liang, Tingyu
Yan, Xiaoyan
Li, Jiye
Lan, Qing
Wang, Jiangfei
Zhao, Jizong
author_facet Wang, Wen
Yang, Fan
Zhang, Lu
Chen, Jing
Zhao, Zheng
Wang, Haoyuan
Wu, Fan
Liang, Tingyu
Yan, Xiaoyan
Li, Jiye
Lan, Qing
Wang, Jiangfei
Zhao, Jizong
author_sort Wang, Wen
collection PubMed
description Anaplastic glioma is Grade III and the median overall survival is about 37.6 months. However, there are still other factors that affect the prognosis for anaplastic glioma patients due to variable overall survival. So we screened four-lncRNA signature (AGAP2-AS1, TPT1-AS1, LINC01198 and MIR155HG) from the lncRNA expression profile from the GSE16011, CGGA and REMBRANDT datasets. The patients in low risk group had longer overall survival than high risk group (median OS 2208.25 vs. 591.30 days; P < 0.0001). Moreover, patients in the low risk group showed similar overall survival to Grade II patients (P = 0.1669), while the high risk group showed significant different to Grade IV (P = 0.0005) with similar trend. So based on the four-lncRNA, the anaplastic gliomas could be divided into grade II-like and grade IV-like groups. On the multivariate analysis, it showed the signature was an independent prognostic factor (P = 0.000). The expression of four lncRNAs in different grades showed that AGAP2-AS1, LINC01198 and MIR155HG were increased with tumor grade, while TPT1-AS1 was decreased. Knockdown of AGAP2-AS1 can inhibit the cell proliferation, migration and invasion, while increase the apoptosis cell rates in vitro. In conclusion, our results showed that the four-lncRNA signature has prognostic value for anaplastic glioma. Moreover, clinicians should conduct corresponding therapies to achieve best treatment with less side effects for two groups patients.
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spelling pubmed-53635822017-03-29 LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas Wang, Wen Yang, Fan Zhang, Lu Chen, Jing Zhao, Zheng Wang, Haoyuan Wu, Fan Liang, Tingyu Yan, Xiaoyan Li, Jiye Lan, Qing Wang, Jiangfei Zhao, Jizong Oncotarget Research Paper Anaplastic glioma is Grade III and the median overall survival is about 37.6 months. However, there are still other factors that affect the prognosis for anaplastic glioma patients due to variable overall survival. So we screened four-lncRNA signature (AGAP2-AS1, TPT1-AS1, LINC01198 and MIR155HG) from the lncRNA expression profile from the GSE16011, CGGA and REMBRANDT datasets. The patients in low risk group had longer overall survival than high risk group (median OS 2208.25 vs. 591.30 days; P < 0.0001). Moreover, patients in the low risk group showed similar overall survival to Grade II patients (P = 0.1669), while the high risk group showed significant different to Grade IV (P = 0.0005) with similar trend. So based on the four-lncRNA, the anaplastic gliomas could be divided into grade II-like and grade IV-like groups. On the multivariate analysis, it showed the signature was an independent prognostic factor (P = 0.000). The expression of four lncRNAs in different grades showed that AGAP2-AS1, LINC01198 and MIR155HG were increased with tumor grade, while TPT1-AS1 was decreased. Knockdown of AGAP2-AS1 can inhibit the cell proliferation, migration and invasion, while increase the apoptosis cell rates in vitro. In conclusion, our results showed that the four-lncRNA signature has prognostic value for anaplastic glioma. Moreover, clinicians should conduct corresponding therapies to achieve best treatment with less side effects for two groups patients. Impact Journals LLC 2016-10-13 /pmc/articles/PMC5363582/ /pubmed/27764782 http://dx.doi.org/10.18632/oncotarget.12624 Text en Copyright: © 2016 Wang et al. http://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
Wang, Wen
Yang, Fan
Zhang, Lu
Chen, Jing
Zhao, Zheng
Wang, Haoyuan
Wu, Fan
Liang, Tingyu
Yan, Xiaoyan
Li, Jiye
Lan, Qing
Wang, Jiangfei
Zhao, Jizong
LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas
title LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas
title_full LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas
title_fullStr LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas
title_full_unstemmed LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas
title_short LncRNA profile study reveals four-lncRNA signature associated with the prognosis of patients with anaplastic gliomas
title_sort lncrna profile study reveals four-lncrna signature associated with the prognosis of patients with anaplastic gliomas
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363582/
https://www.ncbi.nlm.nih.gov/pubmed/27764782
http://dx.doi.org/10.18632/oncotarget.12624
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