The utilization of single-cell sequencing technology in investigating the immune microenvironment of ccRCC

被引:3
作者
Liu, Yuanxin [1 ]
Wu, Guangzhen [1 ]
机构
[1] Dalian Med Univ, Affiliated Hosp 1, Dept Urol, Dalian, Peoples R China
关键词
ScRNA-seq; ccRCC; TME; time; T-cell; TUMOR SIZE; T-CELLS; RNA-SEQ; INTERFERON-ALPHA; RENAL-CARCINOMA; CANCER; SYSTEM; CLASSIFICATION; IDENTIFICATION; HYPERTENSION;
D O I
10.3389/fimmu.2023.1276658
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The growth and advancement of ccRCC are strongly associated with the presence of immune infiltration and the tumor microenvironment, comprising tumor cells, immune cells, stromal cells, vascular cells, myeloid-derived cells, and extracellular matrix (ECM). Nevertheless, as a result of the diverse and constantly evolving characteristics of the tumor microenvironment, prior advanced sequencing methods have frequently disregarded specific less prevalent cellular traits at varying intervals, thereby concealing their significance. The advancement and widespread use of single-cell sequencing technology enable us to comprehend the source of individual tumor cells and the characteristics of a greater number of individual cells. This, in turn, minimizes the impact of intercellular heterogeneity and temporal heterogeneity of the same cell on experimental outcomes. This review examines the attributes of the tumor microenvironment in ccRCC and provides an overview of the progress made in single-cell sequencing technology and its particular uses in the current focus of immune infiltration in ccRCC.
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页数:14
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