Kupffer细胞来源的il - 6通过JAK1-ACAP4途径促进肝细胞癌转移

IF 8.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Tao Li, Xiaoyu Song, Jiena Chen, Yuan Li, Jie Lin, Ping Li, Simiao Yu, Olanrewaju Ayodeji Durojaye, Fengrui Yang, Xing Liu, Jian Li, Shiyuan Cheng, Xuebiao Yao, Xia Ding
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引用次数: 0

摘要

肿瘤相关巨噬细胞(tam)与组织内巨噬细胞不同,因其影响癌症进展和转移的能力而得到认可。然而,肝内巨噬细胞库普弗细胞(KCs)在肝细胞癌(HCC)进展中的具体作用尚不清楚。在这项研究中,我们描述了一种新的机制,即来自HCC细胞的外泌体诱导KCs转变为tam,从而以IL6-JAK1-ACAP4轴依赖的方式促进HCC的转移。从机制上讲,肝癌细胞外泌体介导的KCs的驯化是HCC微环境中IL6产生的主要来源之一。然后,IL6激活JAK1,使其下游效应物ACAP4在Tyr843位点磷酸化,Tyr843位点是在这种情况下发现的一个新的磷酸化位点,这反过来促进ARF6-GTPase活性和肝癌细胞迁移。此外,我们发现肝癌患者肿瘤组织中的IL6水平以及JAK1和ACAP4 Tyr843位点的磷酸化水平明显高于邻近组织。这些发现表明,IL6-JAK1-ACAP4轴可能是HCC的一个有希望的治疗靶点。重要的是,我们筛选了蟾毒灵,一种从蟾毒灵中提取的活性成分,发现它可以抑制JAK1并破坏il6诱导的ACAP4磷酸化。这种抑制不仅损害了肝癌细胞的迁移,而且阻止了HCC的转移。这些发现证明了肝癌细胞与KCs之间通过IL6-JAK1-ACAP4轴相互作用,从而促进HCC转移,揭示了蟾毒灵通过抑制JAK1治疗HCC的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kupffer Cell-derived IL6 Promotes Hepatocellular Carcinoma Metastasis Via the JAK1-ACAP4 Pathway.

Tumor-associated macrophages (TAMs), which differentiate from tissue-resident macrophages, are recognized for their ability to influence cancer progression and metastasis. However, the specific role of Kupffer cells (KCs), the intrinsic macrophages of the liver, in the progression of hepatocellular carcinoma (HCC) remains unclear. In this study, we describe a novel mechanism by which exosomes derived from HCC cells induce KCs to transition into TAMs, thereby facilitating the metastasis of HCC in an IL6-JAK1-ACAP4 axis-dependent manner. Mechanistically, the exosome-mediated domestication of KCs by hepatoma cells constitutes one of the primary sources of IL6 production in the HCC microenvironment. IL6 then activates JAK1 to phosphorylate its downstream effector ACAP4 at Tyr843, a novel phosphorylation site identified in this context, which in turn promotes ARF6-GTPase activity and hepatoma cell migration. Furthermore, we found that the levels of IL6, as well as the phosphorylation of JAK1 and ACAP4 at Tyr843, were significantly greater in tumor tissues from HCC patients than in adjacent tissues. These findings suggest that the IL6-JAK1-ACAP4 axis may be a promising therapeutic target for HCC. Importantly, we screened bufalin, an active ingredient derived from Venenum Bufonis, and discovered that it inhibits JAK1 and disrupts the IL6-induced phosphorylation of ACAP4. This inhibition not only impairs hepatoma cell migration but also prevents the metastasis of HCC. These findings demonstrate the interplay between hepatoma cells and KCs through the IL6-JAK1-ACAP4 axis, thereby promoting HCC metastasis, and reveal the therapeutic potential of bufalin for the treatment of HCC through JAK1 inhibition.

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来源期刊
International Journal of Biological Sciences
International Journal of Biological Sciences 生物-生化与分子生物学
CiteScore
16.90
自引率
1.10%
发文量
413
审稿时长
1 months
期刊介绍: The International Journal of Biological Sciences is a peer-reviewed, open-access scientific journal published by Ivyspring International Publisher. It dedicates itself to publishing original articles, reviews, and short research communications across all domains of biological sciences.
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