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一种新型焦亡相关基因特征在肾母细胞瘤中展现出独特的免疫细胞浸润格局

英文原题:A novel pyroptosis-related gene signature exhibits distinct immune cells infiltration landscape in Wilms' tumor.

PubMed 2024/04/27(内容时间) BMC Pediatr Q2 · IF 2.3(JCR 2025)

研究概要

我们已在WT中建立了一个与细胞焦亡相关的14基因特征。此外,免疫细胞(CD8(+) T细胞、B细胞、Th2细胞、树突状细胞和2型巨噬细胞)的固有作用、差异表达基因的功能(组织/器官发育和细胞间通讯)以及信号通路的状态(癌症中的蛋白聚糖、调控干细胞多能性的信号通路和Wnt信号通路)已被阐明,这些可能在未来被用作治疗靶点。

研究思路结论见上方概要

Wilms瘤(WT)是儿童最常见的肾脏肿瘤。细胞焦亡是一种以炎症为特征且与免疫相关的程序性细胞死亡,已在多种肿瘤中被广泛研究。在本研究中,我们旨在构建一个细胞焦亡相关基因特征,用于预测Wilms瘤的预后。

我们从TARGET肾肿瘤项目中获取RNA-seq数据以构建基因特征,并从GEO数据库获取snRNA-seq数据以验证构建特征的基因。从三个在线数据库中收集了焦亡相关基因(PRGs)。我们通过Lasso Cox回归构建了基因特征,然后建立了列线图。通过免疫细胞浸润分析、差异表达分析和功能富集分析,探讨了基因特征与患者总生存状态相关的潜在机制。

构建了一个由14个PRGs组成的焦亡相关基因特征,其具有中等至高预测能力,1年、3年和5年AUC值分别为0.78、0.80和0.83。通过性别、分期和风险评分建立了预后预测列线图。采用七种算法对肿瘤浸润免疫细胞进行定量,CD8(+) T细胞、B细胞、Th2细胞、树突状细胞和2型巨噬细胞的表达与风险评分呈正相关或负相关。利用两个不同组织学的单核RNA-seq样本进行验证。在各细胞类型中鉴定了特征基因的分布。

展开英文摘要原文

BACKGROUND: Wilms' tumor (WT) is the most common renal tumor in childhood. Pyroptosis, a type of inflammation-characterized and immune-related programmed cell death, has been extensively studied in multiple tumors. In the current study, we aim to construct a pyroptosis-related gene signature for predicting the prognosis of Wilms' tumor. METHODS: We acquired RNA-seq data from TARGET kidney tumor projects for constructing a gene signature, and snRNA-seq data from GEO database for validating signature-constructing genes. Pyroptosis-related genes (PRGs) were collected from three online databases. We constructed the gene signature by Lasso Cox regression and then established a nomogram. Underlying mechanisms by which gene signature is related to overall survival states of patients were explored by immune cell infiltration analysis, differential expression analysis, and functional enrichment analysis. RESULTS: A pyroptosis-related gene signature was constructed with 14 PRGs, which has a moderate to high predicting capacity with 1-, 3-, and 5-year area under the curve (AUC) values of 0.78, 0.80, and 0.83, respectively. A prognosis-predicting nomogram was established by gender, stage, and risk score. Tumor-infiltrating immune cells were quantified by seven algorithms, and the expression of CD8( +) T cells, B cells, Th2 cells, dendritic cells, and type 2 macrophages are positively or negatively correlated with risk score. Two single nuclear RNA-seq samples of different histology were harnessed for validation. The distribution of signature genes was identified in various cell types. CONCLUSIONS: We have established a pyroptosis-related 14-gene signature in WT. Moreover, the inherent roles of immune cells (CD8( +) T cells, B cells, Th2 cells, dendritic cells, and type 2 macrophages), functions of differentially expressed genes (tissue/organ development and intercellular communication), and status of signaling pathways (proteoglycans in cancer, signaling pathways regulating pluripotent of stem cells, and Wnt signaling pathway) have been elucidated, which might be employed as therapeutic targets in the future.

论文信息

作者
Guo Y、Lu W、Zhang Z、Liu H、Zhang A、Zhang T、Wu Y、Li X
第一作者单位
Department of Pediatric Surgery, The Sixth Affiliated Hospital of Harbin Medical University, Harbin Medical University, No.998 Aiying Street, Harbin, Heilongjiang, 150027, China.China
通讯作者单位
Department of Pediatric Surgery, The Sixth Affiliated Hospital of Harbin Medical University, Harbin Medical University, No.998 Aiying Street, Harbin, Heilongjiang, 150027, China. zhaozhu247@163.com.China
文献类型
非美国政府资助研究
期刊
BMC pediatrics2024 Apr 27
原文标识
PubMed 38678251 · DOI 10.1186/s12887-024-04731-0