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10-羟基喜树碱的抗血管生成潜力

Antiangiogenic potential of 10-hydroxycamptothecin.

作者信息

Xiao D, Tan W, Li M, Ding J

机构信息

Division of Anti-tumor Pharmacology, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Science, Chinese Academy of Sciences, PR China.

出版信息

Life Sci. 2001 Aug 24;69(14):1619-28. doi: 10.1016/s0024-3205(01)01236-x.

Abstract

To investigate the antiangiogenic potential of 10-hydroxycamptothecin (HCPT), the proliferation of human microvascular endothelial cells (HMEC) and seven human tumor cell lines were detected by SRB assay, and the endothelial cell migration and tube formation were assessed using two in vitro model systems. Also, inhibition of angiogenesis was determined with a modification of the chick embryo chorioallantoic membrane (CAM) assay in vivo. Morphological assessment of apoptosis was performed by fluorescence microscope. HCPT 0.313-5 micromol x L(-1) treatment resulted in a dose-dependent inhibition of proliferation, migration and tube formation in HMEC cells, and HCPT 6.25-25 nmol x egg(-1) inhibited angiogenesis in CAM assay. HCPT 1.25-5 micromol x L(-1) elicited typical morphological changes of apoptosis including condensed chromatin, nuclear fragmentation, and reduction in volume in HMEC cells. HCPT significantly inhibited angiogenesis both in vitro and in vivo at relatively low concentrations, and this effect was related with induction of apoptosis in HMEC cells. These results taken collectively suggest that HCPT may be a potent antiangiogenetic and cytotoxic drug and further investigation is warranted.

摘要

为研究10-羟基喜树碱(HCPT)的抗血管生成潜力,采用SRB法检测人微血管内皮细胞(HMEC)和7种人肿瘤细胞系的增殖情况,并使用两种体外模型系统评估内皮细胞迁移和管腔形成。此外,通过改良的鸡胚绒毛尿囊膜(CAM)试验在体内测定血管生成的抑制情况。用荧光显微镜对凋亡进行形态学评估。0.313 - 5 μmol·L⁻¹的HCPT处理导致HMEC细胞的增殖、迁移和管腔形成受到剂量依赖性抑制,6.25 - 25 nmol·egg⁻¹的HCPT在CAM试验中抑制血管生成。1.25 - 5 μmol·L⁻¹的HCPT诱导HMEC细胞出现典型的凋亡形态学变化,包括染色质浓缩、核碎裂和体积减小。HCPT在相对较低浓度下在体外和体内均显著抑制血管生成,且这种作用与诱导HMEC细胞凋亡有关。综合这些结果表明,HCPT可能是一种有效的抗血管生成和细胞毒性药物,值得进一步研究。

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