Immune Checkpoint Inhibitor (ICI) Genes and Aging in Clear Cell Renal Cell Carcinoma (ccRCC): Clinical and Genomic Study

被引:10
作者
Al-Danakh, Abdullah [1 ]
Safi, Mohammed [2 ]
Alradhi, Mohammed [3 ]
Chen, Qiwei [1 ]
Baldi, Salem [4 ]
Zhu, Xinqing [1 ]
Yang, Deyong [1 ,5 ]
机构
[1] Dalian Med Univ, Affiliated Hosp 1, Dept Urol, Dalian 116021, Peoples R China
[2] Shandong Univ, Shandong Prov Gen Hosp 2, Dept Resp Dis, Jinan 250023, Peoples R China
[3] Qingdao Binhai Univ, Affiliated Hosp, Dept Urol, Qingdao 266000, Peoples R China
[4] Axbio Biotechnol Shenzhen Co Ltd, Res Ctr Mol Diagnost & Sequencing, Shenzhen 518057, Peoples R China
[5] Healinghands Clin, Dept Surg, Dalian 116021, Peoples R China
关键词
age; immunosenescence; immune checkpoint inhibitors (ICIs); clear cell renal cell carcinoma; TNFSF15; overall survival; CANCER-RISK; TL1A; EXPRESSION;
D O I
10.3390/cells11223641
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: It is anticipated that there will be a large rise in the number of tumor diagnoses and mortality in those aged 65 and older over the course of upcoming decades. Immune checkpoint inhibitors, often known as ICIs, boost immune system activity by selectively targeting ICI genes. On the other hand, old age may be connected with unfavorable results. Methods: The Cancer Genome Atlas (TCGA) provided gene expression data from ccRCC tissue and key clinical variables. ICI gene databases were applied and verified using the GEO database. Results: We identified 14 ICI genes as risk gene signatures among 528 ccRCC patients using univariate and multivariable cox hazard models, and the elderly group was linked with poor survival. Then, by utilizing a new nomogram method, the TNFSF15 gene and age predicting values were estimated at one, three, and five years (85%, 81%, and 81%), respectively, and our age-related risk score was significant even after multivariable analysis (HR = 1.518, p = 0.009, CI = 1.1102.076). TNFSF15 gene expression was lower in elderly ccRCC patients (p = 0.0001). A negative connection between age and the TNFSF15 gene expression was discovered by correlation analysis (p = 0.0001). The verification of the gene by utilizing GEO (GSE167093) with 604 patients was obtained as external validation that showed significant differences in the TNFSF15 gene between young and elderly patients (p = 0.007). Additionally, the protein-protein interactions of the TNFSF15 gene with other ICI genes and aging-related genes was determined. In addition, the TNFSF15 expression was significantly correlated with pathological stages (p = 0.018). Furthermore, it was discovered that the biological processes of senescence, cellular senescence, the immune system, and many immune cell infiltration and immune function types are all closely tied. Conclusions: Along with the risk score evaluation, the ICI gene TNFSF15 was identified as a tumor suppressor gene related to inequalities in age survival and is associated with pathological stages and different immunity statuses. The aging responses of ccRCC patients and related gene expression need further investigation in order to identify potential therapeutic targets.
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页数:15
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