Macrophage efferocytosis mediated by the TP63-RAC2 pathway promotes immunosuppressive remodeling in esophageal cancer

This study explores the role of efferocytosis in esophageal squamous cell carcinoma (ESCC) using single-cell RNA sequencing and in vitro/in vivo assays. Analyzing 27 samples from 9 patients with ESCC, we identify diverse cell types and significant heterogeneity in the tumor microenvironment, with a focus on efferocytosis. Our findings highlight that macrophages engulf apoptotic tumor cells, thereby impairing immune responses and promoting tumor progression. Notably, TP63 and RAC2 emerge as key regulators of this process, influencing efferocytosis and immune modulation. Functional assays demonstrate that disrupting these pathways alters macrophage efferocytosis and impacts tumor growth in vivo. These results suggest that targeting efferocytosis pathways offers potential therapeutic strategies for ESCC, enhancing antitumor immunity and improving patient outcomes. The study underscores the complex interactions between tumor cells and the immune system, with efferocytosis representing a promising therapeutic target.

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Publication Details

Journal
Cell Reports Medicine
Published
2025-12-19
DOI
https://doi.org/10.1016/j.xcrm.2025.102529
Citations
1
Primary Topic
Phagocytosis and Immune Regulation
Type
article
Field-Weighted Citation Impact
0.80
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article

Macrophage efferocytosis mediated by the TP63-RAC2 pathway promotes immunosuppressive remodeling in esophageal cancer

1 citations
Cell Reports Medicine
Phagocytosis and Immune Regulation
0.80
article

Macrophage efferocytosis mediated by the TP63-RAC2 pathway promotes immunosuppressive remodeling in esophageal cancer

article en
1 citations

Abstract

This study explores the role of efferocytosis in esophageal squamous cell carcinoma (ESCC) using single-cell RNA sequencing and in vitro/in vivo assays. Analyzing 27 samples from 9 patients with ESCC, we identify diverse cell types and significant heterogeneity in the tumor microenvironment, with a focus on efferocytosis. Our findings highlight that macrophages engulf apoptotic tumor cells, thereby impairing immune responses and promoting tumor progression. Notably, TP63 and RAC2 emerge as key regulators of this process, influencing efferocytosis and immune modulation. Functional assays demonstrate that disrupting these pathways alters macrophage efferocytosis and impacts tumor growth in vivo. These results suggest that targeting efferocytosis pathways offers potential therapeutic strategies for ESCC, enhancing antitumor immunity and improving patient outcomes. The study underscores the complex interactions between tumor cells and the immune system, with efferocytosis representing a promising therapeutic target.

Cell Reports MedicineVol. 7(1)
Ningbo University (CN), Nanchang University (CN), City University of Hong Kong (HK), Shanghai Jiao Tong University (CN), Yunnan University (CN), Peking University (CN), Fudan University (CN), University of Malaya (MY), Wuhan University (CN), Liuzhou General Hospital (CN), Shanghai Ninth People's Hospital (CN), Ningbo Medical Center Lihuili Hospital (CN), Zhongshan Hospital (CN), Second Affiliated Hospital of Xi'an Jiaotong University (CN), Fourth Affiliated Hospital of Guangxi Medical University (CN), Renmin Hospital of Wuhan University (CN), First Affiliated Hospital of Nanchang University (CN), State Key Laboratory of Natural and Biomimetic Drugs (CN), Yunnan University of Traditional Chinese Medicine (CN), Universidade Nova de Lisboa (PT)
Openalex Percentile: Top 20%
Phagocytosis and Immune Regulation
0.80
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