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异欧前胡素通过抑制VEGFR2信号通路抑制血管生成。

Isoimperatorin Inhibits Angiogenesis by Suppressing VEGFR2 Signaling Pathway.

作者信息

Xu Yating, Xia Di, Deng Shan, Liang Minglu

机构信息

Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Ave, Wuhan, 430022, China.

Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Cardiovasc Drugs Ther. 2025 Apr;39(2):275-286. doi: 10.1007/s10557-024-07561-5. Epub 2024 Feb 16.

Abstract

PURPOSE

Angiogenesis involves in many pathological processes, including tumor metastasis, diabetic retinopathy, and rheumatoid arthritis. Therefore, identifying therapeutic drugs that target angiogenesis may be a promising strategy for disease treatment. Isoimperatorin is a furanocoumarin with anti-inflammatory and anti-microbial effects. However, the impacts of isoimperatorin on angiogenesis and its underlying mechanisms remain unclear. This study aimed to verify its effects on vascular endothelial growth factor (VEGF)-induced endothelial angiogenesis.

METHODS

We employed various assays including 5-ethynyl-2'-deoxyuridine incorporation assay, transwell migration assay, wound healing assay, tube formation assay, and Western blot to evaluate the effects of isoimperatorin on angiogenesis in vitro. Additionally, we utilized Western blot and immunofluorescence analysis to examine the activation of vascular endothelial growth factor receptor (VEGFR) 2 and its downstream signaling pathways following isoimperatorin treatment. To further validate the anti-angiogenic effects of isoimperatorin in vivo, we conducted a matrigel plug assay and established an orthotopic tumor model.

RESULTS

We demonstrated that pretreatment with isoimperatorin inhibited VEGF-induced endothelial cell proliferation, migration, and tube formation. Isoimperatorin also suppressed angiogenesis in vivo in a matrigel plug assay and in an orthotopic tumor model. Our results revealed that isoimperatorin exhibited anti-angiogenic effects via inhibiting VEGFR2 and its downstream signaling pathways activation.

CONCLUSIONS

Our study showed that isoimperatorin suppressed angiogenesis by targeting the VEGFR2 signaling pathway and could be a potential therapeutic agent for targeting angiogenesis.

摘要

目的

血管生成参与许多病理过程,包括肿瘤转移、糖尿病视网膜病变和类风湿性关节炎。因此,鉴定靶向血管生成的治疗药物可能是一种有前景的疾病治疗策略。异欧前胡素是一种具有抗炎和抗菌作用的呋喃香豆素。然而,异欧前胡素对血管生成的影响及其潜在机制仍不清楚。本研究旨在验证其对血管内皮生长因子(VEGF)诱导的内皮血管生成的影响。

方法

我们采用了多种检测方法,包括5-乙炔基-2'-脱氧尿苷掺入检测、Transwell迁移检测、伤口愈合检测、管腔形成检测和蛋白质印迹法,以评估异欧前胡素对体外血管生成的影响。此外,我们利用蛋白质印迹法和免疫荧光分析来检测异欧前胡素处理后血管内皮生长因子受体(VEGFR)2及其下游信号通路的激活情况。为了进一步验证异欧前胡素在体内的抗血管生成作用,我们进行了基质胶栓检测并建立了原位肿瘤模型。

结果

我们证明,异欧前胡素预处理可抑制VEGF诱导的内皮细胞增殖、迁移和管腔形成。异欧前胡素在基质胶栓检测和原位肿瘤模型中也抑制了体内血管生成。我们的结果表明,异欧前胡素通过抑制VEGFR2及其下游信号通路的激活而表现出抗血管生成作用。

结论

我们的研究表明,异欧前胡素通过靶向VEGFR2信号通路抑制血管生成,可能是一种潜在的靶向血管生成的治疗药物。

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