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肿瘤相关巨噬细胞来源的 S100 钙结合蛋白 A9 增强肝癌干细胞样特性。

S100 calcium-binding protein A9 from tumor-associated macrophage enhances cancer stem cell-like properties of hepatocellular carcinoma.

机构信息

Department of General Surgery, Huashan Hospital, Cancer Metastasis Institute, Fudan University, Shanghai, China.

Institutes of Biomedical Sciences, Fudan University, Shanghai, China.

出版信息

Int J Cancer. 2021 Mar 1;148(5):1233-1244. doi: 10.1002/ijc.33371. Epub 2020 Nov 17.

Abstract

Tumor-associated macrophages (TAMs) are crucial components of the tumor microenvironment. They play vital roles in hepatocellular carcinoma (HCC) progression. However, the interactions between TAMs and HCC cells have not been fully characterized. In this study, TAMs were induced using human monocytic cell line THP-1 cells in vitro to investigate their functions in HCC progression. S100 calcium-binding protein A9 (S100A9), an inflammatory microenvironment-related secreted protein, was identified to be significantly upregulated in TAMs. S100A9 expression in tumor tissues was associated with poor survival of HCC patients. It could enhance the stem cell-like properties of HepG2 and MHCC-97H cells by activating nuclear factor-kappa B signaling pathway through advanced glycosylation end product-specific receptor in a Ca -dependent manner. Furthermore, we found that, after treatment with S100A9, HepG2 and MHCC-97H cells recruited more macrophages via chemokine (CC motif) ligand 2, which suggests a positive feedback between TAMs and HCC cells. Taken together, our findings reveal that TAMs could upregulate secreted protein S100A9 and enhance the stem cell-like properties of HCC cells and provide a potential therapeutic target for combating HCC.

摘要

肿瘤相关巨噬细胞(TAMs)是肿瘤微环境的重要组成部分。它们在肝细胞癌(HCC)的进展中起着至关重要的作用。然而,TAMs 与 HCC 细胞之间的相互作用尚未得到充分表征。在这项研究中,我们使用人单核细胞系 THP-1 细胞在体外诱导 TAMs,以研究它们在 HCC 进展中的功能。发现 S100 钙结合蛋白 A9(S100A9),一种与炎症微环境相关的分泌蛋白,在 TAMs 中显著上调。肿瘤组织中 S100A9 的表达与 HCC 患者的不良预后相关。它可以通过激活核因子-κB 信号通路,通过晚期糖基化终产物特异性受体在 Ca2+依赖性方式增强 HepG2 和 MHCC-97H 细胞的干细胞样特性。此外,我们发现,在用 S100A9 处理后,HepG2 和 MHCC-97H 细胞通过趋化因子(C-C 基元)配体 2 招募更多的巨噬细胞,这表明 TAMs 和 HCC 细胞之间存在正反馈。总之,我们的研究结果表明,TAMs 可以上调分泌蛋白 S100A9,并增强 HCC 细胞的干细胞样特性,并为对抗 HCC 提供了一个潜在的治疗靶点。

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