Comprehensive analysis of a new prognosis signature based on histone deacetylases in clear cell renal cell carcinoma

被引:11
|
作者
Cheng, Fajuan [1 ,2 ]
Zheng, Bin [3 ,4 ,5 ]
Wang, Jianwei [6 ]
Zhao, Guiting [4 ,5 ]
Yao, Zhongshun [4 ,5 ]
Niu, Zhihong [4 ,5 ]
He, Wei [4 ,5 ]
机构
[1] Shandong Univ, Shandong Prov Hosp, Dept Nephrol, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Cheeloo Coll Med, Shandong Prov Hosp, Dept Nephrol, Jinan, Shandong, Peoples R China
[3] Shandong Univ, Cheeloo Coll Med, Jinan, Shandong, Peoples R China
[4] Shandong First Med Univ, Shandong Prov Hosp, Dept Urol, Jinan, Shandong, Peoples R China
[5] Shandong Univ, Shandong Prov Hosp, Dept Urol, Jinan, Shandong, Peoples R China
[6] Shandong Univ, Shandong Prov ENT Hosp, Dept Urol, Jinan, Shandong, Peoples R China
来源
CANCER MEDICINE | 2021年 / 10卷 / 18期
关键词
histone deacetylase; overall survival; prognosis; renal cell carcinoma; signature; CANCER; EXPRESSION; APOPTOSIS; PROLIFERATION; DEGRADATION; EPIGENETICS; SUPPRESSION; INHIBITORS; MECHANISM; RELEVANCE;
D O I
10.1002/cam4.4156
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:6503 / 6514
页数:12
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