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Erschienen in: Cancer Immunology, Immunotherapy 1/2022

24.05.2021 | Original Article

Construction of TME and Identification of crosstalk between malignant cells and macrophages by SPP1 in hepatocellular carcinoma

verfasst von: Lulu Liu, Ruyi Zhang, Jingwen Deng, Xiaomeng Dai, Xudong Zhu, Qihan Fu, Hangyu Zhang, Zhou Tong, Peng Zhao, Weijia Fang, Yi Zheng, Xuanwen Bao

Erschienen in: Cancer Immunology, Immunotherapy | Ausgabe 1/2022

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Abstract

Liver cancer accounts for 6% of all malignancies causing death worldwide, and hepatocellular carcinoma (HCC) is the most common histological type. HCC is a heterogeneous cancer, but how the tumour microenvironment (TME) of HCC contributes to the progression of HCC remains unclear. In this study, we investigated the immune microenvironment by multiomics analysis. The tumour immune infiltration characteristics of HCC were determined at the genomic, epigenetic, bulk transcriptome and single-cell levels by data from The Cancer Genome Atlas portal and the Gene Expression Omnibus (GEO). An epigenetic immune-related scoring system (EIRS) was developed to stratify patients with poor prognosis. SPP1, one gene in the EIRS system, was identified as an immune-related predictor of poor survival in HCC patients. Through receptor-ligand pair analysis in single-cell RNA-seq, SPP1 was indicated to mediate the crosstalk between HCC cells and macrophages via SPP1-CD44 and SPP1-PTGER4 association. In vitro experiments further validate SPP1 can trigger the polarization of macrophages to M2-phenotype tumour-associated macrophages (TAMs).
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Metadaten
Titel
Construction of TME and Identification of crosstalk between malignant cells and macrophages by SPP1 in hepatocellular carcinoma
verfasst von
Lulu Liu
Ruyi Zhang
Jingwen Deng
Xiaomeng Dai
Xudong Zhu
Qihan Fu
Hangyu Zhang
Zhou Tong
Peng Zhao
Weijia Fang
Yi Zheng
Xuanwen Bao
Publikationsdatum
24.05.2021
Verlag
Springer Berlin Heidelberg
Erschienen in
Cancer Immunology, Immunotherapy / Ausgabe 1/2022
Print ISSN: 0340-7004
Elektronische ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-021-02967-8

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