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单细胞分析整合揭示肝癌肿瘤相关巨噬细胞图谱。

Integrated Single Cell Analysis Reveals An Atlas of Tumor Associated Macrophages in Hepatocellular Carcinoma.

机构信息

Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.

Institute of Organ Donation and Transplantation, Medical College of Qingdao University, Qingdao, China.

出版信息

Inflammation. 2024 Dec;47(6):2077-2093. doi: 10.1007/s10753-024-02026-1. Epub 2024 Apr 26.

Abstract

Hepatocellular carcinoma (HCC), one of the most prevalent cancers globally, is closely associated with tumor-associated macrophages (TAMs), including monocyte-derived macrophages and liver-resident Kupffer cells. Understanding TAM heterogeneity at the cellular level is crucial for developing effective HCC prevention and treatment strategies. In this study, we conducted an integrated single-cell analysis of four cohorts (GSE140228, GSE125449, GSE149614 and GSE156625) to elucidate the TAM landscape in HCC. We identified 284 gene markers, termed Panmyeloid markers, that characterize myeloid cells within this context. Our analysis distinguished six clusters of monocyte-derived macrophages (Macro1-Macro6) and four clusters of Kupffer cells (Kupffer1-Kupffer4). Notably, CXCL10 + macrophages and MT1G + Kupffer cells, predominantly located within tumor tissues, exhibited distinct functional characteristics relevant to HCC. We also explored cellular communication between TAMs and T cells, uncovering potential signaling pathways such as the CXCL10/CXCL11-CXCR3 and CXCL12-CXCR4 networks. These findings enhance our understanding of TAMs in HCC and open new avenues for targeted therapeutic interventions.

摘要

肝细胞癌(HCC)是全球最常见的癌症之一,与肿瘤相关巨噬细胞(TAMs)密切相关,包括单核细胞衍生的巨噬细胞和肝驻留的库普弗细胞。了解 TAM 在细胞水平上的异质性对于开发有效的 HCC 预防和治疗策略至关重要。在这项研究中,我们对四个队列(GSE140228、GSE125449、GSE149614 和 GSE156625)进行了综合单细胞分析,以阐明 HCC 中的 TAM 景观。我们确定了 284 个基因标记,称为 Panmyeloid 标记,这些标记特征在于该背景下的髓样细胞。我们的分析区分了六个单核细胞衍生的巨噬细胞簇(Macro1-Macro6)和四个库普弗细胞簇(Kupffer1-Kupffer4)。值得注意的是,CXCL10+巨噬细胞和 MT1G+库普弗细胞主要位于肿瘤组织中,表现出与 HCC 相关的独特功能特征。我们还探索了 TAMs 和 T 细胞之间的细胞通讯,揭示了潜在的信号通路,如 CXCL10/CXCL11-CXCR3 和 CXCL12-CXCR4 网络。这些发现增强了我们对 HCC 中 TAMs 的理解,并为靶向治疗干预开辟了新途径。

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