The anti-angiogenic and anti-vasculogenic mimicry effects of GN25 in endothelial and glioma cells

IF 4.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhi-Hong Wen , Long Chang , San-Nan Yang , Chen-Ling Yu , Fang-Yu Tung , Hsiao-Mei Kuo , I-Chen Lu , Chang-Yi Wu , Po-Chang Shih , Wu-Fu Chen , Nan-Fu Chen
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引用次数: 0

Abstract

Background and purpose

Scientists have been exploring anti-angiogenic strategies to inhibit angiogenesis and prevent tumor growth. Vasculogenic mimicry (VM) in glioblastoma multiforme (GBM) poses a challenge, complicating anti-angiogenesis therapy. A novel drug, GN25 (3-[{1,4-dihydro-5,8-dimethoxy-1,4-dioxo-2-naphthalenyl}thio]-propanoic acid), can inhibit tumor formation. This study aims to investigate the microenvironmental effects and molecular mechanisms of GN25 in anti-angiogenesis and anti-VM.

Experimental approach

MTT (3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide) assay was used to evaluate the cell viability of different concentrations of GN25 in human umbilical vein endothelial cells (HUVEC) and Uppsala 87 malignant glioma (U87MG) cells. Functional assays were used to investigate the effects of GN25 on angiogenesis-related processes, whereas gelatin zymography, enzyme-linked immunosorbent assays, and Western blotting were utilized to assess the influence on matrix metalloproteinase (MMP)-2 and vascular endothelial growth factor (VEGF) secretion and related signaling pathways.

Key results

GN25 suppressed migration, wound healing, and tube formation in HUVECs and disrupted angiogenesis in a rat aorta ring and zebrafish embryo model. GN25 dose-dependently reduced phosphatidylinositol 3-kinase/AKT and inhibited MMP-2/VEGF secretion in HUVECs. In U87MG cells, GN25 inhibited migration, wound healing, and VM, accompanied by a decrease in MMP-2 and VEGF secretion. The results indicate that GN25 effectively inhibits angiogenesis and VM formation in HUVECs and U87MG cells without affecting preexisting vascular structures.

Conclusion and implications

This study elaborated GN25's potential as an anti-angiogenic agent by elucidating its inhibitory effects on classical angiogenesis. VM provides valuable insights for developing novel therapeutic strategies against tumor progression and angiogenesis-related diseases. These results indicate the potential of GN25 as a promising candidate for angiogenesis-related diseases.

Abstract Image

GN25 在内皮细胞和胶质瘤细胞中的抗血管生成和抗血管生成模拟作用。
背景和目的:科学家们一直在探索抑制血管生成和防止肿瘤生长的抗血管生成策略。多形性胶质母细胞瘤(GBM)中的血管生成模拟(VM)带来了挑战,使抗血管生成治疗变得复杂。一种新型药物 GN25(3-[{1,4-二氢-5,8-二甲氧基-1,4-二氧代-2-萘基}硫]-丙酸)可抑制肿瘤的形成。本研究旨在探讨 GN25 在抗血管生成和抗肿瘤方面的微环境效应和分子机制:实验方法:采用 MTT(3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide)试验评估不同浓度 GN25 在人脐静脉内皮细胞(HUVEC)和乌普萨拉 87 恶性胶质瘤(U87MG)细胞中的细胞活力。功能试验用于研究 GN25 对血管生成相关过程的影响,而明胶酶谱法、酶联免疫吸附试验和 Western 印迹法则用于评估 GN25 对基质金属蛋白酶(MMP)-2 和血管内皮生长因子(VEGF)分泌及相关信号通路的影响:GN25抑制了HUVECs的迁移、伤口愈合和管形成,并破坏了大鼠主动脉环和斑马鱼胚胎模型中的血管生成。GN25 可剂量依赖性地减少磷脂酰肌醇 3- 激酶/AKT,抑制 HUVEC 中 MMP-2/VEGF 的分泌。在 U87MG 细胞中,GN25 可抑制迁移、伤口愈合和血管内皮生长因子,同时降低 MMP-2 和血管内皮生长因子的分泌。结果表明,GN25能有效抑制HUVECs和U87MG细胞的血管生成和VM形成,而不影响原有的血管结构:本研究通过阐明GN25对经典血管生成的抑制作用,阐述了其作为抗血管生成药物的潜力。VM 为开发针对肿瘤进展和血管生成相关疾病的新型治疗策略提供了有价值的见解。这些结果表明,GN25 有潜力成为治疗血管生成相关疾病的候选药物。
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来源期刊
CiteScore
10.00
自引率
2.00%
发文量
151
审稿时长
44 days
期刊介绍: BBA Molecular Cell Research focuses on understanding the mechanisms of cellular processes at the molecular level. These include aspects of cellular signaling, signal transduction, cell cycle, apoptosis, intracellular trafficking, secretory and endocytic pathways, biogenesis of cell organelles, cytoskeletal structures, cellular interactions, cell/tissue differentiation and cellular enzymology. Also included are studies at the interface between Cell Biology and Biophysics which apply for example novel imaging methods for characterizing cellular processes.
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