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Single‐cell landscape of malignant ascites from patients with metastatic colorectal cancer
(D) Differential gene expression reveals significantly up-regulated and down-regulated genes in 11 cell types between PD and SD patients. (G) Dot plots show communication probability of the interactions between cell populations in pmCRC ascites (The dot size is proportional to the contribution score...
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Published in: | Cancer communications (London, England) England), 2024-07, Vol.44 (7), p.713-717 |
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creator | Zhou, Haiyang Yin, Jiahui Wang, Anqi Yin, Xiaomao Jin, Taojun Xu, Kai Zhu, Lin Wang, Jiexuan Wang, Wenqiang Zhang, Wei Li, Xinxiang Hu, Zhiqian Li, Xinxing |
description | (D) Differential gene expression reveals significantly up-regulated and down-regulated genes in 11 cell types between PD and SD patients. (G) Dot plots show communication probability of the interactions between cell populations in pmCRC ascites (The dot size is proportional to the contribution score computed from pattern recognition analysis.). Differentially expressed genes and gene ontology (GO) analyses showed that the “cell-cell adhesion”, “inflammatory response”, and “cytokine production” were differentially enriched between primary tumors and ascites (Supplementary Figure S1D), which implied that the liquid state of ascites changed the functions of the fibroblast populations. Because the expression pattern of the “M2” marker gene CD163 perfectly coincided with that of LAIR1 in all sub-clusters (Figure 1M), we postulated that the immunosuppressive function of tumor-associated macrophages (TAMs) might be exerted via LAIR1. |
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(G) Dot plots show communication probability of the interactions between cell populations in pmCRC ascites (The dot size is proportional to the contribution score computed from pattern recognition analysis.). Differentially expressed genes and gene ontology (GO) analyses showed that the “cell-cell adhesion”, “inflammatory response”, and “cytokine production” were differentially enriched between primary tumors and ascites (Supplementary Figure S1D), which implied that the liquid state of ascites changed the functions of the fibroblast populations. Because the expression pattern of the “M2” marker gene CD163 perfectly coincided with that of LAIR1 in all sub-clusters (Figure 1M), we postulated that the immunosuppressive function of tumor-associated macrophages (TAMs) might be exerted via LAIR1.</description><identifier>ISSN: 2523-3548</identifier><identifier>EISSN: 2523-3548</identifier><identifier>DOI: 10.1002/cac2.12541</identifier><identifier>PMID: 38532531</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Antigens ; Ascites ; Cancer therapies ; Cell death ; Chemokines ; Colorectal cancer ; Extracellular matrix ; Fibroblasts ; Gene expression ; Genomes ; Hepatitis ; Immunoglobulins ; Letter to the Journal ; Leukocytes ; Ligands ; Lymphocytes ; Medical prognosis ; Metastasis ; Patients ; Tumors</subject><ispartof>Cancer communications (London, England), 2024-07, Vol.44 (7), p.713-717</ispartof><rights>2024 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Sun Yat‐sen University Cancer Center.</rights><rights>2024. 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(G) Dot plots show communication probability of the interactions between cell populations in pmCRC ascites (The dot size is proportional to the contribution score computed from pattern recognition analysis.). Differentially expressed genes and gene ontology (GO) analyses showed that the “cell-cell adhesion”, “inflammatory response”, and “cytokine production” were differentially enriched between primary tumors and ascites (Supplementary Figure S1D), which implied that the liquid state of ascites changed the functions of the fibroblast populations. 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(G) Dot plots show communication probability of the interactions between cell populations in pmCRC ascites (The dot size is proportional to the contribution score computed from pattern recognition analysis.). Differentially expressed genes and gene ontology (GO) analyses showed that the “cell-cell adhesion”, “inflammatory response”, and “cytokine production” were differentially enriched between primary tumors and ascites (Supplementary Figure S1D), which implied that the liquid state of ascites changed the functions of the fibroblast populations. 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subjects | Antigens Ascites Cancer therapies Cell death Chemokines Colorectal cancer Extracellular matrix Fibroblasts Gene expression Genomes Hepatitis Immunoglobulins Letter to the Journal Leukocytes Ligands Lymphocytes Medical prognosis Metastasis Patients Tumors |
title | Single‐cell landscape of malignant ascites from patients with metastatic colorectal cancer |
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