三七粉通过调节 MKK6/p38 信号通路,抑制缺氧诱导的肝癌细胞促血管生成。

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacy and Pharmacology Pub Date : 2024-04-03 DOI:10.1093/jpp/rgad086
Zhe Chen, Man Wang, Xiang Lv, Yannan Xu, Xionghui Wang, Bai Li, Changquan Ling, Juan Du
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引用次数: 0

摘要

目的:三七末(SSM)是一种治疗晚期肝细胞癌(HCC)的传统中药配方。本研究旨在探讨三七粉对 HCC 诱导的血管生成的影响及其潜在机制:在1%氧气环境中用HCC细胞条件培养基培养内皮细胞,以模拟肿瘤缺氧微环境。EA.hy926 细胞的迁移和肾小管生成是通过肾小管形成和划痕法检测的。蛋白芯片用于检测Huh7细胞中的SSM靶向蛋白。我们还建立了一个动物模型来观察 SSM 对体内血管生成的影响:结果:数据表明,在缺氧条件下,低剂量的 SSM 可减少 HCC 诱导的 EA.hy926 细胞迁移和管形成。这些作用的部分原因可能是抑制了 HIF-1α 诱导的血管内皮生长因子α在 Huh7 细胞中的表达。此外,这种抑制是以 MKK6/P38 依赖性的方式进行的。此外,裸鼠Huh7皮下肿瘤模型进一步证明,SSM对肿瘤重量的抑制作用可能部分是通过阻断MKK6/P38信号通路减少血管生成而实现的:结论:在缺氧条件下,SSM通过抑制MKK6/P38信号通路抑制HCC诱导的血管生成,有利于HCC肿瘤的生长。
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Sanshimao formula inhibits the hypoxia-induced pro-angiogenesis of hepatocellular carcinoma cells partly through regulating MKK6/p38 signaling pathway.

Objectives: Sanshimao (SSM) is a traditional Chinese medicine formula for advanced hepatocellular carcinoma (HCC). This study was designed to investigate the effect of SSM on HCC-induced angiogenesis and to explore the potential mechanism.

Methods: The endothelial cells were cultured with HCC cells conditioned medium in the 1% oxygen atmosphere to imitate tumor hypoxia microenvironment. EA.hy926 cells migration and tubulogenesis were detected by tube formation and scratch-wound assay. The protein microarray was employed to explore SSM-targeted proteins in Huh7 cells. We also established an animal model to observe the effects of SSM on angiogenesis in vivo.

Results: The data indicated that SSM reduced HCC-induced migration and tube formation of EA.hy926 cells at low dose under hypoxic conditions. These effects might be partly owing to suppression of HIF-1α-induced vascular endothelial growth factorα expression in Huh7 cells. Moreover, this inhibition was in an MKK6/P38-dependent way. Besides, Huh7 subcutaneous tumor models in nude mice further demonstrated the inhibition of SSM on tumor weight might be exerted partly by reduction of angiogenesis via blocking MKK6/P38 signaling pathways.

Conclusion: SSM inhibits HCC-induced pro-angiogenesis under hypoxic conditions via suppression of MKK6/P38 signaling pathways, which is favorable for HCC tumor growth.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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