青蒿琥酯通过HIF-1 α/ VEGF/PDGF途径抑制脉络膜黑色素瘤的血管生成模拟。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Qing-yue Ma , Xiao-yan Xu , Yuan-zhang Zhu, Ning-ning Yao, Yi-chong Liu, Xiao-di Gao, Qian Zhang, Wen-juan Luo
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引用次数: 0

摘要

脉络膜黑色素瘤(CM)是一种高度转移性眼部肿瘤,在缺氧诱导的血管生成作用下表现出血管生成模拟(VM)。本研究探讨了抗疟疾药物青蒿琥酯(ART)通过调节 HIF-1α/VEGF/PDGF 通路对 CM VM 的抑制作用。免疫组化(IHC)证实了血管内皮生长因子(VEGF)和表皮生长因子(PDGF)表达升高的 CM 中的血管瘤。缺氧促进了 CM 的增殖,上调了 HIF-1α、VEGF 和 PDGF。VEGF 和 PDGF 增强了 CM 的迁移、侵袭和 VM,其中 HIF-1α 起着关键作用。ART通过抑制HIF-1α/VEGF/PDGF通路缓解了VM的形成,突出了其作为CM抗肿瘤药物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artesunate inhibits vasculogenic mimicry in choroidal melanoma through HIF-1 α/ VEGF/PDGF pathway

Choroidal melanoma (CM), a highly metastatic eye tumor, exhibits vasculogenic mimicry (VM) facilitated by hypoxia-induced angiogenesis. This study explored the inhibitory impact of the anti-malarial drug Artesunate (ART) on CM VM through modulation of the HIF-1α/VEGF/PDGF pathway. Immunohistochemistry (IHC) confirmed VM in CM with elevated VEGF and PDGF expression. Hypoxia promoted CM proliferation, upregulating HIF-1α, VEGF and PDGF. VEGF and PDGF enhanced CM migration, invasion and VM, with HIF-1α playing a crucial role. ART mitigated VM formation by suppressing the HIF-1α/VEGF/PDGF pathway, highlighting its potential as an anti-tumor agent in CM.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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