Comprehensive Analysis of the Expression and Prognosis Value of Chromobox Family Members in Clear Cell Renal Cell Carcinoma

被引:16
|
作者
Zhu, Yuanyuan [1 ,2 ,3 ]
Pu, Zhangya [4 ,5 ]
Li, Zhenfen [2 ]
Lin, Ying [6 ]
Li, Ning [1 ]
Peng, Fang [1 ,2 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Blood Transfus, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Natl Hlth Commiss NHC Key Lab Canc Prote, Changsha, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Dept Infect Dis, Changsha, Peoples R China
[5] Cent South Univ, Xiangya Hosp, Hunan Key Lab Viral Hepatitis, Changsha, Peoples R China
[6] Cent South Univ, Xiangya Hosp, Dept Nucl Med, Changsha, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
基金
中国国家自然科学基金;
关键词
chromobox; biomarker; prognosis; bioinformatics analysis; clear cell renal cell carcinoma; GENE-EXPRESSION; BREAST-CANCER; LUNG ADENOCARCINOMA; ONCOGENIC ACTIVITY; TUMOR PROGRESSION; POOR-PROGNOSIS; WEB SERVER; CBX4; PROLIFERATION; CONTRIBUTES;
D O I
10.3389/fonc.2021.700528
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clear cell renal cell carcinoma (ccRCC) accounts for 80% of all renal cancers and has a poor prognosis. Chromobox (CBX) family protein expression has been reported in a variety of human malignancies, but the roles of CBXs in ccRCC remain unclear. In this study, by using ONCOMINE, UALCAN, GEPIA, Kaplan-Meier Plotter, cBioPortal, and TIMER, we found the transcriptional levels of CBX3 and CBX4 in ccRCC tissues were significantly higher than those in normal kidney tissues, whereas the transcriptional levels of CBX1, CBX5, CBX6, and CBX7 were significantly reduced in ccRCC tissues. The promoters of CBX2, CBX3, CBX4, CBX5, CBX6, CBX7, and CBX8 were hypermethylated, whereas the CBX1 promoter was hypomethylated in ccRCC. The expression of CBX1, CBX3, CBX4, CBX5, CBX6, and CBX7 was significantly associated with clinicopathological parameters in ccRCC patients. ccRCC patients with high expression levels of CBX3, CBX4, and CBX8 and low expression levels of CBX1, CBX5, CBX6, and CBX7 showed a strong association with poor overall survival. Genetic alterations in CBXs were correlated with poor overall survival and disease-free survival in patients with ccRCC. Moreover, we found significant associations between the expression of CBXs and infiltration of immune cells (B cells, CD8+ T cells, CD4+ T cells, macrophages, neutrophils, and dendritic cells). Our results provide novel insights into the development of CBX-based biomarkers and therapeutic targets for ccRCC.
引用
收藏
页数:19
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