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Comprehensive analysis of a new prognosis signature based on histone deacetylases in clear cell renal cell carcinoma.
Cheng, Fajuan; Zheng, Bin; Wang, Jianwei; Zhao, Guiting; Yao, Zhongshun; Niu, Zhihong; He, Wei.
Afiliación
  • Cheng F; Department of Nephrology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China.
  • Zheng B; Department of Nephrology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
  • Wang J; Cheeloo College of Medicine, Shandong University, Jinan, Shandong, P.R. China.
  • Zhao G; Department of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, P.R. China.
  • Yao Z; Department of Urology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, P.R. China.
  • Niu Z; Department of Urology, Shandong Provincial ENT Hospital Affiliated to Shandong University, Jinan, Shandong, P.R. China.
  • He W; Department of Urology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, P.R. China.
Cancer Med ; 10(18): 6503-6514, 2021 09.
Article en En | MEDLINE | ID: mdl-34308568
Histone deacetylases (HDAC) family is vital for tumorigenesis and tumor progression. However, the exact role of the HDAC family in clear cell renal cell carcinoma (ccRCC) remains unclear. Based on The Cancer Genome Atlas (TCGA), International Cancer Genome Consortium (ICGC), and The Human Protein Atlas (HPA) database, we investigated and validated the expression profile, clinical significance and prognostic value of HDAC family members in ccRCC. Moreover, we further explored the correlation between HDACs and tumor microenvironment, tumor stemness, drug activity and immune subtype. The HDAC8, HDAC10, and HDAC11 manifested potential clinical value for prognosis, and the correlation analyses reveals underlying molecular mechanisms, which deserve further investigation for ccRCC. This Integrated bioinformatics analysis, based on transcriptomics and proteomics, implied that HDAC8, HDAC10, and HDAC11 may serve as potential molecular biomarkers and therapeutic targets for ccRCC, but some underlying molecular mechanisms still need to be elucidated.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Represoras / Carcinoma de Células Renales / Biomarcadores de Tumor / Histona Desacetilasas / Neoplasias Renales Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Med Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Represoras / Carcinoma de Células Renales / Biomarcadores de Tumor / Histona Desacetilasas / Neoplasias Renales Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Med Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos