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癌症基因组图谱转录组TIL免疫特征的泛癌比较分析

A Pan-Cancer Comparative Analysis of The Cancer Genome Atlas Transcriptomic TIL-Immune Signatures.

作者信息

Hitscherich Kyle, Noussome Darryl, Dinerman Aaron, Dulemba Victoria, Lowery Frank, Nilubol Naris

机构信息

National Cancer Institute.

出版信息

Res Sq. 2025 Apr 25:rs.3.rs-6441170. doi: 10.21203/rs.3.rs-6441170/v1.

Abstract

Efforts to understand the tumor microenvironment (TME) through basic science research and The Cancer Genome Atlas (TCGA) data analysis have led to the creation of unique immune transcriptomic signatures from tumor-infiltrating lymphocytes (TIL). However, no pan-cancer analysis has been conducted to compare the prognostic performance of these signatures using overall survival (OS) or progression-free interval (PFI) as endpoints. We compiled a library of 146 TIL-immune signatures and evaluated gene signature score correlation with OS and PFI for 9,961 available TCGA samples across 33 cancer types. Zhang CD8 TCS demonstrated higher accuracy in prognosticating both OS and PFI across the pan-cancer landscape, however, variability was seen across cancer types and germ cell origin. Cluster analysis compiled a group of six signatures (Oh.Cd8.MAIT, Grog.8KLRB1, Oh.TIL_CD4.GZMK, Grog.CD4.TCF7, Oh.CD8.RPL, Grog.CD4.RPL32) whose association with OS and PFI could potentially be conserved across multiple cancer types.

摘要

通过基础科学研究和癌症基因组图谱(TCGA)数据分析来了解肿瘤微环境(TME)的努力,已促使从肿瘤浸润淋巴细胞(TIL)中创建了独特的免疫转录组特征。然而,尚未进行全癌分析以使用总生存期(OS)或无进展生存期(PFI)作为终点来比较这些特征的预后性能。我们编制了一个包含146个TIL免疫特征的文库,并评估了基因特征分数与33种癌症类型的9961个可用TCGA样本的OS和PFI的相关性。Zhang CD8 TCS在全癌范围内对OS和PFI进行预后预测时显示出更高的准确性,然而,在不同癌症类型和生殖细胞起源中存在变异性。聚类分析汇总了一组六个特征(Oh.Cd8.MAIT、Grog.8KLRB1、Oh.TIL_CD4.GZMK、Grog.CD4.TCF7、Oh.CD8.RPL、Grog.CD4.RPL32),其与OS和PFI的关联可能在多种癌症类型中保持一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f1f/12045360/593b5ceb4bf6/nihpp-rs6441170v1-f0001.jpg

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