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Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer

Bladder cancer (BLCA) is one of the most common urological cancer with increasing cases and deaths every year. In the present study, we aim to construct an immune‐related prognostic lncRNA signature (IRPLS) in bladder cancer (BLCA) patients and explore its immunogenomic implications in pan‐cancers....

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Autores principales: Luo, Wen‐Jie, Tian, Xi, Xu, Wen‐Hao, Qu, Yuan‐Yuan, Zhu, Wen‐Kai, Wu, Jie, Ma, Chun‐Guang, Zhang, Hai‐Liang, Ye, Ding‐Wei, Zhu, Yi‐Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093983/
https://www.ncbi.nlm.nih.gov/pubmed/33797188
http://dx.doi.org/10.1111/jcmm.16494
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author Luo, Wen‐Jie
Tian, Xi
Xu, Wen‐Hao
Qu, Yuan‐Yuan
Zhu, Wen‐Kai
Wu, Jie
Ma, Chun‐Guang
Zhang, Hai‐Liang
Ye, Ding‐Wei
Zhu, Yi‐Ping
author_facet Luo, Wen‐Jie
Tian, Xi
Xu, Wen‐Hao
Qu, Yuan‐Yuan
Zhu, Wen‐Kai
Wu, Jie
Ma, Chun‐Guang
Zhang, Hai‐Liang
Ye, Ding‐Wei
Zhu, Yi‐Ping
author_sort Luo, Wen‐Jie
collection PubMed
description Bladder cancer (BLCA) is one of the most common urological cancer with increasing cases and deaths every year. In the present study, we aim to construct an immune‐related prognostic lncRNA signature (IRPLS) in bladder cancer (BLCA) patients and explore its immunogenomic implications in pan‐cancers. First, the immune‐related differentially expressed lncRNAs (IRDELs) were identified by ‘limma’ R package and the score of IRPLS in every patient were evaluated by Cox regression. The dysregulation of IRDELs expression between cancer and para‐cancer normal tissues was validated through RT‐qPCR. Then, we further explore the biological functions of a novel lncRNA from IRPLS, RP11‐89 in BLCA using CCK8 assay, Transwell assay and Apoptosis analysis, which indicated that RP11‐89 was able to promote cell proliferation and invasive capacity while inhibits cell apoptosis in BLCA. In addition, we performed bioinformatic methods and RIP to investigate and validate the RP11‐89/miR‐27a‐3p/PPARγ pathway in order to explore the mechanism. Next, CIBERSORT and ESTIMATE algorithm were used to evaluate abundance of tumour‐infiltrating immune cells and scores of tumour environment elements in BLCA with different level of IRPLS risk scores. Finally, multiple bioinformatic methods were performed to show us the immune landscape of these four lncRNAs for pan‐cancers. In conclusion, this study first constructed an immune‐related prognostic lncRNA signature, which consists of RP11‐89, PSORS1C3, LINC02672 and MIR100HG and might shed lights on novel targets for individualized immunotherapy for BLCA patients.
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spelling pubmed-80939832021-05-10 Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer Luo, Wen‐Jie Tian, Xi Xu, Wen‐Hao Qu, Yuan‐Yuan Zhu, Wen‐Kai Wu, Jie Ma, Chun‐Guang Zhang, Hai‐Liang Ye, Ding‐Wei Zhu, Yi‐Ping J Cell Mol Med Original Articles Bladder cancer (BLCA) is one of the most common urological cancer with increasing cases and deaths every year. In the present study, we aim to construct an immune‐related prognostic lncRNA signature (IRPLS) in bladder cancer (BLCA) patients and explore its immunogenomic implications in pan‐cancers. First, the immune‐related differentially expressed lncRNAs (IRDELs) were identified by ‘limma’ R package and the score of IRPLS in every patient were evaluated by Cox regression. The dysregulation of IRDELs expression between cancer and para‐cancer normal tissues was validated through RT‐qPCR. Then, we further explore the biological functions of a novel lncRNA from IRPLS, RP11‐89 in BLCA using CCK8 assay, Transwell assay and Apoptosis analysis, which indicated that RP11‐89 was able to promote cell proliferation and invasive capacity while inhibits cell apoptosis in BLCA. In addition, we performed bioinformatic methods and RIP to investigate and validate the RP11‐89/miR‐27a‐3p/PPARγ pathway in order to explore the mechanism. Next, CIBERSORT and ESTIMATE algorithm were used to evaluate abundance of tumour‐infiltrating immune cells and scores of tumour environment elements in BLCA with different level of IRPLS risk scores. Finally, multiple bioinformatic methods were performed to show us the immune landscape of these four lncRNAs for pan‐cancers. In conclusion, this study first constructed an immune‐related prognostic lncRNA signature, which consists of RP11‐89, PSORS1C3, LINC02672 and MIR100HG and might shed lights on novel targets for individualized immunotherapy for BLCA patients. John Wiley and Sons Inc. 2021-04-01 2021-05 /pmc/articles/PMC8093983/ /pubmed/33797188 http://dx.doi.org/10.1111/jcmm.16494 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Luo, Wen‐Jie
Tian, Xi
Xu, Wen‐Hao
Qu, Yuan‐Yuan
Zhu, Wen‐Kai
Wu, Jie
Ma, Chun‐Guang
Zhang, Hai‐Liang
Ye, Ding‐Wei
Zhu, Yi‐Ping
Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer
title Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer
title_full Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer
title_fullStr Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer
title_full_unstemmed Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer
title_short Construction of an immune‐related LncRNA signature with prognostic significance for bladder cancer
title_sort construction of an immune‐related lncrna signature with prognostic significance for bladder cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093983/
https://www.ncbi.nlm.nih.gov/pubmed/33797188
http://dx.doi.org/10.1111/jcmm.16494
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