Immune Gene Signature Expression Differs between African American and Caucasian Patients with Renal Cell Carcinoma

IF 1.1 Q4 ONCOLOGY Kidney Cancer Pub Date : 2022-04-22 DOI:10.3233/kca-220003
P. Ghatalia, Aangi J Shah, M. Slifker
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Abstract

BACKGROUND: Predictive immune signatures such as the T-effector, the 26-gene “Renal 101 Immuno signature” and the 18-gene T-cell inflamed gene expression profile were developed in clinical trials enrolling predominantly Caucasians and there is a dearth of literature comparing tumor biology between African American (AA) and Caucasian patients. OBJECTIVE: To compare the immune gene signature expression in AA (n = 55) and Caucasian (n = 457) patients. METHODS: Raw gene expression count data were downloaded from the TCGA KIRC dataset and tumor samples from “white” and “black or AA” patients were selected. The gene expression values of the immune signatures were VST-transformed normalized counts and compared between the groups. RESULTS: There were 457 Caucasian and 55 AA patients in the TCGA. The immune gene expression in all three signatures was significantly lower in AA patients compared to Caucasians (p <  0.05). We validated our findings in an independent dataset using Nanostring Immune Profile Panel. Since the majority of AA tumors in TCGA were stage I (71%), we compared gene expression between stage I AA tumors (n = 39) with stage I Caucasian tumors (n = 220). Once again, the immune gene expression was significantly lower in AA patients compared to Caucasians (p <  0.05), indicating differences in tumor biology between the races. CONCLUSIONS: Low expression of predictive immune gene signatures in AA compared to Caucasian patients indicates a possible difference in the biology of their tumors. Future studies are needed to validate our findings in other datasets and to study the predictive role of these signatures in AA patients.
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非裔美国人和白种人肾细胞癌患者免疫基因特征表达差异
背景:预测性免疫特征,如t效应、26基因“肾101免疫特征”和18基因t细胞炎症基因表达谱,主要是在白种人的临床试验中开发出来的,并且缺乏比较非裔美国人(AA)和白种人患者肿瘤生物学的文献。目的:比较AA (n = 55)和高加索(n = 457)患者的免疫基因特征表达。方法:从TCGA KIRC数据集中下载原始基因表达计数数据,并选择“白人”和“黑人或AA”患者的肿瘤样本。免疫特征基因表达值为vst转化归一化计数,组间比较。结果:TCGA患者中白人457例,AA 55例。与白种人相比,AA患者三个特征的免疫基因表达均显著降低(p < 0.05)。我们使用Nanostring Immune Profile Panel在一个独立的数据集中验证了我们的发现。由于TCGA中大部分AA肿瘤为I期(71%),我们比较了I期AA肿瘤(n = 39)与I期高加索肿瘤(n = 220)的基因表达。同样,AA患者的免疫基因表达明显低于白种人(p < 0.05),说明种族间肿瘤生物学存在差异。结论:与高加索患者相比,AA患者预测性免疫基因信号的低表达可能表明其肿瘤生物学差异。未来的研究需要在其他数据集中验证我们的发现,并研究这些特征在AA患者中的预测作用。
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来源期刊
Kidney Cancer
Kidney Cancer Multiple-
CiteScore
0.90
自引率
8.30%
发文量
23
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