Measuring the composition of the tumor microenvironment with transcriptome analysis: past, present and future

被引:5
|
作者
Zhang, Han [1 ]
Lu, Xinghua [1 ,2 ]
Lu, Binfeng [3 ]
Gullo, Giuseppe [4 ]
Chen, Lujia [1 ]
机构
[1] Univ Pittsburgh, Dept Biomed Informat, Pittsburgh, PA 15206 USA
[2] UPMC Hillman Canc Ctr, Pittsburgh, PA 15232 USA
[3] Hackensack Meridian Hlth, Ctr Discovery & Innovat, Nutley, NJ 07110 USA
[4] Univ Palermo, Villa Sofia Cervello Hosp, Dept Obstet & Gynecol, I-90146 Palermo, Italy
关键词
bulk-RNAseq; cell-cell network; deconvolution; immune phenotype; immunotherapy; scRNAseq; spatial transcriptome; TME subtype; tumor microenvironment; OX40; AGONIST; CELL-DEATH; IMMUNOTHERAPY; RADIOTHERAPY; COMBINATION; AUTOPHAGY; IMMUNITY;
D O I
10.2217/fon-2023-0658
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Interactions between tumor cells and immune cells in the tumor microenvironment (TME) play a vital role the mechanisms of immune evasion, by which cancer cells escape immune elimination. Thus, the characterization and quantification of different components in the TME is a hot topic in molecular biology and drug discovery. Since the development of transcriptome sequencing in bulk tissue, single cells and spatial dimensions, there are increasing methods emerging to deconvolute and subtype the TME. This review discusses and compares such computational strategies and downstream subtyping analyses. Integrative analyses of the transcriptome with other data, such as epigenetics and T-cell receptor sequencing, are needed to obtain comprehensive knowledge of the dynamic TME.
引用
收藏
页码:1207 / 1220
页数:14
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