Suppr超能文献

悬钩子总生物碱在体内和体外均表现出抗血管生成活性。

Total alkaloids of Rubus alceifolius Poir shows anti-angiogenic activity in vivo and in vitro.

机构信息

Fujian University of Traditional Chinese Medicine, Fuzhou, People's Republic of China.

Fujian University of Traditional Chinese Medicine, Fuzhou, People's Republic of China

出版信息

Integr Cancer Ther. 2014 Nov;13(6):520-8. doi: 10.1177/1534735414547109. Epub 2014 Aug 22.

Abstract

Total alkaloids is an active ingredient of the natural plant Rubus alceifolius Poir, commonly used for the treatment of various cancers. Antitumor effects may be mediated through anti-angiogenic mechanisms. As such, the goal of the present study was to investigate and evaluate the effect of total alkaloids in Rubus alceifolius Poir (TARAP) on tumor angiogenesis and investigate the underlying molecular mechanisms of TARAP action in vivo and in vitro. A chick embryo chorioallantoic membrane (CAM) assay was used to assess angiogenesis in vivo. An MTT assay was performed to determine the viability of human umbilical vein endothelial cells (HUVECs) with and without treatment. Cell cycle progression of HUVECs was examined by FACS analysis with propidium iodide staining. HUVEC migration was determined using a scratch wound method. Tube formation of HUVECs was assessed with an ECMatrix gel system, and mRNA and protein expression of VEGF-A in both HUVECs and HepG2 human hepatocellular carcinoma cells were examined by RT-PCR and ELISA, respectively. Our results showed that TARAP inhibited angiogenesis in the CAM model in vivo and inhibited HUVEC proliferation via blocking cell cycle G1 to S progression in a dose- and time-dependent manners in vitro. Moreover, TARAP inhibited HUVEC migration and tube formation and downregulated mRNA and protein expression of VEGF-A in both HepG2 cells and HUVECs. Our findings suggest that the anti-angiogenic activity of TARAP may partly contribute to its antitumor properties and may be valuable for the treatment of diseases involving pathologic angiogenesis such as cancer.

摘要

总生物碱是天然植物茅莓的一种活性成分,常用于治疗各种癌症。其抗肿瘤作用可能是通过抗血管生成机制介导的。因此,本研究旨在探讨和评估茅莓总生物碱(TARAP)对肿瘤血管生成的影响,并在体内和体外研究 TARAP 作用的潜在分子机制。鸡胚绒毛尿囊膜(CAM)试验用于评估体内血管生成。MTT 法测定 TARAP 处理前后人脐静脉内皮细胞(HUVEC)的活力。碘化丙啶染色通过 FACS 分析检测 HUVEC 的细胞周期进程。划痕法检测 HUVEC 的迁移。ECMatrix 凝胶系统评估 HUVEC 的管形成,并用 RT-PCR 和 ELISA 分别检测 HUVEC 和 HepG2 人肝癌细胞中 VEGF-A 的 mRNA 和蛋白表达。结果表明,TARAP 抑制体内 CAM 模型中的血管生成,并通过阻断细胞周期 G1 到 S 进展,以剂量和时间依赖的方式在体外抑制 HUVEC 增殖。此外,TARAP 抑制 HUVEC 的迁移和管形成,并下调 HepG2 细胞和 HUVEC 中 VEGF-A 的 mRNA 和蛋白表达。我们的研究结果表明,TARAP 的抗血管生成活性可能部分归因于其抗肿瘤特性,对于治疗涉及病理性血管生成的疾病(如癌症)可能具有重要价值。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验