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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.
Afiliação
  • Luo WJ; Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Tian X; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Xu WH; Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Qu YY; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Zhu WK; Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Wu J; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Ma CG; Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Zhang HL; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
  • Ye DW; Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
  • Zhu YP; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
J Cell Mol Med ; 25(9): 4326-4339, 2021 05.
Article em En | MEDLINE | ID: mdl-33797188
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Biomarcadores Tumorais / RNA Longo não Codificante Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Bexiga Urinária / Biomarcadores Tumorais / RNA Longo não Codificante Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article