CCL5 might be a prognostic biomarker and associated with immuno-therapeutic efficacy in cancers: A pan-cancer analysis

被引:8
|
作者
Huang, Yanchun [1 ,2 ]
Wu, Lijuan [3 ]
Sun, Yong [1 ,2 ]
Li, Jiwen [1 ,2 ]
Mao, Nan [4 ,5 ]
Yang, Yeqing [6 ]
Zhao, Ming [5 ,7 ]
Ren, Sichong [4 ,5 ]
机构
[1] First Peoples Hosp Longquanyi Dist, Dept Lab Med, Chengdu 610100, Peoples R China
[2] Sichuan Univ, Dept Lab Med, West China Longquan Hosp, Chengdu 610100, Peoples R China
[3] Sichuan Univ, Dept Lab Med, West China Hosp, Chengdu 610041, Peoples R China
[4] Chengdu Med Coll, Clin Med Coll, Dept Nephrol, Chengdu 610500, Peoples R China
[5] Chengdu Med Coll, Affiliated Hosp 1, Chengdu 610500, Peoples R China
[6] Southwest Med Univ, Dept Oncol, Affiliated Hosp Tradit Chinese Med, Luzhou 646000, Peoples R China
[7] Chengdu Med Coll, Clin Med Coll, Dept Gastroenterol, Chengdu 610500, Peoples R China
基金
中国国家自然科学基金;
关键词
TUMOR MICROENVIRONMENT; HOST-DEFENSE; CHEMOKINES; CELLS; CCR5; CCL5/RANTES; EXPRESSION; RECEPTORS; TARGET;
D O I
10.1016/j.heliyon.2023.e18215
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose: Chemokine ligand 5 (CCL5), a vital member of the CC chemokine family, plays diverse roles in tumorigenesis, metastasis, and prognosis in various human tumors. However, no pan-cancer analysis has been conducted to illustrate its distinctive effects on clinical prognosis via underlying mechanisms and biological characteristics.Methods: Herein, we exploited the existed public bioinformatics database, primarily TCGA database and GTEx data, to comprehensively analyze the value of CCL5 involved in patient prognosis. Results: This study found that CCL5 was excessively expressed in most tumors and significantly associated with clinical prognosis in 10 out of 33 types of tumors. Notably, CCL5 might be an independent predictive biomarker of clinical outcome in SKCM patients, confirmed by univariate and multivariate Cox regression analysis. Furthermore, we acquired the genetic alteration status of CCL5 in multiple types of tumor tissues from TCGA cohorts. We revealed a potential correlation between the expression level of CCL5 and tumor mutational burden in 33 types of tumors. In addition, data showed that DNA methylation was associated with CCL5 gene expression in THCA, PRAD, LUSC, and BRCA cancers. Immune infiltration and immune checkpoints are fine indexes for evaluating immunotherapy. We uncovered that CCL5 was negatively correlated with the immune infiltration of CD8+ T cell, CD4+ T cell, macrophages, and gamma delta T cells in BRCA-basal and CESC tumors, while a significant positive correlation was observed in BLCA, COAD and other 7 types of tumors. Besides, CCL5 was closely associated with the immune checkpoint molecules in 8 types of tumors. The TIDE score was less in the CCL5 high-expressed group than in the CCL5 low-expressed group in SKCM patients, which indicated that CCL5 might be a fine monitor of immune response for immunotherapy. GO enrichment analysis data uncovered that cytokine-cytokine receptor interaction and chemokine signaling might be involved in the role of CCL5 in regulating tumor pathogenesis and prognosis.Conclusion: In conclusion, CCL5 was preliminarly identified as a biomarker of immune response and prognosis for tumors patients via our first comprehensive pan-cancer analysis.
引用
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页数:16
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