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S1PR1在VEGF外泌体介导的肝细胞癌抗血管生成治疗耐药中的作用

Role of S1PR1 in VEGF-exosomes mediated resistance of hepatocellular carcinoma to anti-angiogenesis therapy.

作者信息

Yao Xinghong, Tang Min, Li Liang, Zeng Ye

机构信息

Department of Radiotherapy, Precision Radiation in Oncology Key Laboratory of Sichuan Province, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Center, Sichuan Cancer Hospital & Institute, University of Electronic Science and Technology of China, Chengdu, 610041, China.

Institute of Biomedical Engineering, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, Chengdu, 610041, China.

出版信息

Cancer Cell Int. 2025 Jul 16;25(1):264. doi: 10.1186/s12935-025-03907-7.

Abstract

BACKGROUND

Anti-angiogenesis therapy (AAT) triggers vascular endothelial growth factor (VEGF)-exosomes secretion from tumor-associated endothelial cells (TAECs) for hepatocellular carcinoma (HCC) tubulogenesis and metastasis. Sphingosine-1-phosphate receptor 1 (S1PR1) has been implicated in HCC progression, but it was targeted by microRNA-9 (miR-9) that might mediate the formation of TAECs. This study aims to investigate the role of miR-9 and VEGF-exosomes in S1PR1-mediated HCC progression and resistance to AAT.

METHODS

The expression and distribution of miR-9 in HCC tissues were analyzed using qRT-PCR and fluorescence in situ hybridization (FISH). The impact of S1PR1 knockdown on VEGF-exosome uptake, as well as miR-9 and VEGF-exosome-induced epithelial-mesenchymal transition (EMT), migration, and invasion of HCC cells, was assessed by Transwell assays, fluorescence microscopy, and Western blotting.

RESULTS

miR-9 expression was significantly upregulated in HCC tissues and selectively localized in CD34⁺ endothelial cells within paracancerous microvessels, suggesting its role in TAEC transformation.miR-9 promoted EMT and enhanced HCC cell migration and invasion, effects that were further potentiated by VEGF-exosomes. S1PR1 knockdown significantly inhibited VEGF-exosome uptake and suppressed miR-9- and VEGF-exosome-induced EMT, migration, and invasion of HCC cells.

CONCLUSION

In conclusion, miR-9 facilitates HCC progression by enhancing tumor malignancy and promoting AAT resistance through TAEC-mediated VEGF-exosome secretion. S1PR1 is a critical mediator of this process, and its inhibition represents a potential therapeutic strategy to overcome AAT resistance in HCC.

摘要

背景

抗血管生成疗法(AAT)可触发肿瘤相关内皮细胞(TAECs)分泌血管内皮生长因子(VEGF)-外泌体,以促进肝细胞癌(HCC)的血管生成和转移。鞘氨醇-1-磷酸受体1(S1PR1)与HCC进展有关,但其受微小RNA-9(miR-9)靶向,而miR-9可能介导TAECs的形成。本研究旨在探讨miR-9和VEGF-外泌体在S1PR1介导的HCC进展及对AAT耐药中的作用。

方法

采用qRT-PCR和荧光原位杂交(FISH)分析miR-9在HCC组织中的表达和分布。通过Transwell实验、荧光显微镜和蛋白质印迹法评估S1PR1敲低对VEGF-外泌体摄取的影响,以及miR-9和VEGF-外泌体诱导的HCC细胞上皮-间质转化(EMT)、迁移和侵袭。

结果

miR-9在HCC组织中表达显著上调,并选择性地定位于癌旁微血管内的CD34⁺内皮细胞,提示其在TAEC转化中的作用。miR-9促进EMT并增强HCC细胞的迁移和侵袭,VEGF-外泌体进一步增强了这些作用。S1PR1敲低显著抑制VEGF-外泌体摄取,并抑制miR-9和VEGF-外泌体诱导的HCC细胞EMT、迁移和侵袭。

结论

总之,miR-9通过增强肿瘤恶性程度并通过TAEC介导的VEGF-外泌体分泌促进AAT耐药,从而促进HCC进展。S1PR1是这一过程的关键介质,抑制S1PR1代表了一种克服HCC中AAT耐药的潜在治疗策略。

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