CENPF as a Potential Biomarker Associated with the Immune Microenvironment of Renal Cancer.

IF 2.7 4区 医学 Q3 ONCOLOGY
Technology in Cancer Research & Treatment Pub Date : 2025-01-01 Epub Date: 2025-03-31 DOI:10.1177/15330338251330791
Meilin Chen, Xiuxin Tang, YanPing Liang, Tangdang Ding, Meifang He, Dong Wang, Ruizhi Wang
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Abstract

IntroductionRenal cancer, particularly Kidney Renal Clear Cell Carcinoma (KIRC), remains a major clinical challenge due to its aggressive nature and poor prognosis. Identifying reliable biomarkers for tumor progression and survival is critical for improving patient outcomes. This study aimed to investigate the role of Centromere Protein F (CENPF) as a potential prognostic biomarker for renal cancer.MethodData from the TCGA database, including Kidney Chromophobe (KICH), Kidney Renal Papillary Cell Carcinoma (KIRP), and KIRC, were analyzed to identify differentially expressed genes. Molecular Complex Detection (MCODE) was used to identify significant gene modules among upregulated genes, and univariate Cox regression analyses assessed the prognostic value of hub genes. Retrospective qPCR was conducted on tissue and plasma samples from KIRC patients to validate findings. Single-cell sequencing data from the GSE159115 dataset were analyzed, and the CIBERSORT algorithm was applied to evaluate the composition of tumor immune infiltrating cells (TIICs).ResultsCENPF was identified as a hub gene significantly upregulated in renal cancer subtypes, with overexpression linked to worse survival outcomes in KIRC patients. Retrospective qPCR confirmed high CENPF expression was associated with poorer prognosis. Single-cell sequencing revealed that CENPF is predominantly expressed in T-cell clusters. TIIC analysis showed a negative correlation between CENPF and resting mast cells, but positive correlations with follicular helper T-cells and memory-activated CD4T-cells. Prognostic analysis indicated that high follicular helper T-cell expression predicted poorer survival, while high plasma cell expression correlated with better outcomes.ConclusionCENPF plays a critical role in tumor progression and the modulation of the tumor immune microenvironment in KIRC. These findings suggest that CENPF could serve as a valuable prognostic biomarker and potential target for therapeutic intervention in renal cancer.

CENPF作为肾癌免疫微环境相关的潜在生物标志物。
肾癌,特别是肾透明细胞癌(KIRC),由于其侵袭性和预后差,仍然是一个主要的临床挑战。确定肿瘤进展和生存的可靠生物标志物对于改善患者预后至关重要。本研究旨在探讨着丝粒蛋白F (CENPF)作为肾癌潜在预后生物标志物的作用。方法分析TCGA数据库中的数据,包括肾憎色症(KICH)、肾乳头状细胞癌(KIRP)和KIRC,以鉴定差异表达基因。采用分子复合物检测(MCODE)技术鉴定上调基因中的显著基因模块,单变量Cox回归分析评估枢纽基因的预后价值。回顾性qPCR对KIRC患者的组织和血浆样本进行验证。分析来自GSE159115数据集的单细胞测序数据,并应用CIBERSORT算法评估肿瘤免疫浸润细胞(TIICs)的组成。结果发现,在肾癌亚型中,scenpf是一个显著上调的枢纽基因,在KIRC患者中,过表达与较差的生存结果相关。回顾性qPCR证实,高表达的CENPF与较差的预后相关。单细胞测序显示,CENPF主要在t细胞簇中表达。TIIC分析显示,CENPF与静止肥大细胞呈负相关,但与滤泡辅助t细胞和记忆激活cd4t细胞呈正相关。预后分析表明,高滤泡辅助性t细胞表达预示较差的生存,而高浆细胞表达与较好的预后相关。结论cenpf在KIRC的肿瘤进展和肿瘤免疫微环境调节中起关键作用。这些发现表明,CENPF可以作为一种有价值的预后生物标志物和治疗干预的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
202
审稿时长
2 months
期刊介绍: Technology in Cancer Research & Treatment (TCRT) is a JCR-ranked, broad-spectrum, open access, peer-reviewed publication whose aim is to provide researchers and clinicians with a platform to share and discuss developments in the prevention, diagnosis, treatment, and monitoring of cancer.
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