Circ-0044539通过外泌体-miR-29a-3p促进肝细胞癌的淋巴结转移

IF 8.1 1区 生物学 Q1 CELL BIOLOGY
Yi Yang, Xue-Qin Chen, Ya-Xun Jia, Jie Ma, Di Xu, Zuo-Lin Xiang
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引用次数: 0

摘要

淋巴结转移(LNM)是肝细胞癌(HCC)的常见浸润性特征,与不良的临床预后有关。通过微阵列分析和生物信息学分析,我们发现circ-0044539-miR-29a-3p-VEGFA轴是HCC淋巴结转移进展的潜在关键因素。在 HCC 细胞和裸鼠中,circ-0044539 的下调或 miR-29a-3p 的上调与肿瘤体积小、PI3K-AKT-mTOR 通路失活以及 LNM 关键因子(HIF-1α 和 CXCR4)的下调有关。此外,circ-0044539还负责外泌体miR-29a-3p的分泌。随后观察到外泌体miR-29a-3p迁移到LN,并下调多形核髓源性抑制细胞(PMN-MDSCs)中的高迁移率组盒转录因子1(Hbp1),从而诱导形成适合肿瘤定植的微环境。总之,circ-0044539通过外泌体促进了HCC细胞的LNM能力,并诱导了LNs中的免疫抑制环境,凸显了其作为HCC LNM和HCC免疫疗法靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Circ-0044539 promotes lymph node metastasis of hepatocellular carcinoma through exosomal-miR-29a-3p.

Circ-0044539 promotes lymph node metastasis of hepatocellular carcinoma through exosomal-miR-29a-3p.

Lymph node metastasis (LNM) is a common invasive feature of hepatocellular carcinoma (HCC) associated with poor clinical outcomes. Through microarray profiling and bioinformatic analyses, we identified the circ-0044539-miR-29a-3p-VEGFA axis as a potential key factor in the progression of HCC LNM. In HCC cells and nude mice, circ-0044539 downregulation or miR-29a-3p upregulation was associated with small tumor size, PI3K-AKT-mTOR pathway inactivation, and downregulation of the key LNM factors (HIF-1α and CXCR4). Furthermore, circ-0044539 was also responsible for exosomal miR-29a-3p secretion. Exosomal miR-29a-3p was then observed to migrate to the LNs and downregulate High-mobility group box transcription factor 1 (Hbp1) in Polymorphonuclear Myeloid-derived suppressor cells (PMN-MDSCs), inducing the formation of a microenvironment suitable for tumor colonization. Overall, circ-0044539 promotes HCC cell LNM abilities and induces an immune-suppressive environment in LNs through exosomes, highlighting its potential as a target for HCC LNM and HCC immunotherapy.

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来源期刊
Cell Death & Disease
Cell Death & Disease CELL BIOLOGY-
CiteScore
15.10
自引率
2.20%
发文量
935
审稿时长
2 months
期刊介绍: Brought to readers by the editorial team of Cell Death & Differentiation, Cell Death & Disease is an online peer-reviewed journal specializing in translational cell death research. It covers a wide range of topics in experimental and internal medicine, including cancer, immunity, neuroscience, and now cancer metabolism. Cell Death & Disease seeks to encompass the breadth of translational implications of cell death, and topics of particular concentration will include, but are not limited to, the following: Experimental medicine Cancer Immunity Internal medicine Neuroscience Cancer metabolism
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