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Identification of Immune-Related Subtypes and Construction of a Novel Prognostic Model for Bladder Urothelial Cancer.
Zhang, Jiange; Huang, Caisheng; Yang, Rirong; Wang, Xiang; Fang, Bo; Mi, Junhao; Yuan, Hao; Mo, Zengnan; Sun, Yihai.
  • Zhang J; Department of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
  • Huang C; Center for Genomic and Personalized Medicine, Guangxi Medical University, Nanning 530021, China.
  • Yang R; Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Nanning 530021, China.
  • Wang X; Guangxi Key Laboratory for Genomic and Personalized Medicine, Guangxi Key Laboratory of Colleges and Universities, Nanning 530021, China.
  • Fang B; Department of Urology, The Second Affiliated Hospital of Guangxi Medical University, Nanning 530007, China.
  • Mi J; Department of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
  • Yuan H; Center for Genomic and Personalized Medicine, Guangxi Medical University, Nanning 530021, China.
  • Mo Z; Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Nanning 530021, China.
  • Sun Y; Guangxi Key Laboratory for Genomic and Personalized Medicine, Guangxi Key Laboratory of Colleges and Universities, Nanning 530021, China.
Biomolecules ; 12(11)2022 11 11.
Article en En | MEDLINE | ID: mdl-36421685
ABSTRACT
The purpose of this study was to explore the relationship between bladder urothelial cancer (BLCA) and immunity, to screen prognosis-related immune genes (PIGs), and to construct an immune-related prognosis model (IRPM). We processed the relevant data of The Cancer Genome Atlas (TCGA-BLCA) and GSE13507 using R software and Perl. We divided BLCA into high-immunity and low-immunity subtypes. There were significant differences in the two subtypes. In addition, we identified 13 PIGs of BLCA by jointly analyzing the gene expression data and survival information of GSE13507 and TCGA-BLCA, and constructed IRPM through nine of them. The low-risk group had better survival outcome than the high-risk group. We also constructed a nomogram based on clinicopathological information and risk scores of the patients. Moreover, the prognosis of BLCA patients was significantly impacted by the expression of almost every gene used to calculate the risk score. The result of real-time fluorescence quantitative polymerase chain reaction revealed that all the genes used to calculate the risk score were differentially expressed between BLCA and adjacent normal tissues, except PDGFRA. Our research provided potential targets for the treatment of BLCA and a reference for judging the prognosis of BLCA.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Vejiga Urinaria / Carcinoma de Células Transicionales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Vejiga Urinaria / Carcinoma de Células Transicionales Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article