Laboratory of Immunopharmacology and Experimental Therapeutics, Division of Cancer Research, Regional Cancer Centre, Medical College Post, Thiruvananthapuram, Kerala, 695011, India; Research Centre, University of Kerala, India.
Laboratory of Immunopharmacology and Experimental Therapeutics, Division of Cancer Research, Regional Cancer Centre, Medical College Post, Thiruvananthapuram, Kerala, 695011, India; Research Centre, University of Kerala, India.
Biochem Biophys Res Commun. 2023 Sep 17;673:106-113. doi: 10.1016/j.bbrc.2023.05.056. Epub 2023 May 25.
Angiogenesis is a vital process for tumor growth and metastasis. Inhibition of angiogenesis is a promising strategy in cancer treatment. In this study, we analyzed the anti-angiogenic activity of AS1411 functionalized Withaferin A encapsulated PEGylated nanoliposomes (ALW) using both in vitro and in vivo models. AS1411 aptamer functionalized nanoliposomes are an efficient drug delivery system for carrying chemotherapeutic agents to target cancer cells, and Withaferin A (WA) is a steroidal lactone known for potent anti-angiogenic activity. ALW showed significant inhibition in the migration and tube formation of endothelial cells, which are critical events in angiogenesis. In vivo angiogenesis study using ALW showed remarkable inhibition of tumor-directed capillary formation by altered serum cytokines, VEGF, GM-CSF, and NO levels. ALW treatment downregulated the gene expression of Matrix metalloproteinase (MMP)-2, MMP-9, VEGF, NF-kB and upregulated the expression of tissue inhibitor of metalloproteinase (TIMP)-1. Our results demonstrate that ALW inhibits tumor-specific angiogenesis by gene expression of NF-κB, VEGF, MMP-2, and MMP-9. The present study shows that using ALW can offer an attractive strategy for inhibiting tumor angiogenesis.
血管生成是肿瘤生长和转移的关键过程。抑制血管生成是癌症治疗中很有前途的策略。在这项研究中,我们使用体外和体内模型分析了 AS1411 功能化 Withaferin A 包封的聚乙二醇化纳米脂质体(ALW)的抗血管生成活性。AS1411 适体功能化纳米脂质体是一种有效的药物递送系统,可将化疗药物靶向输送到癌细胞,而 Withaferin A(WA)是一种具有强大抗血管生成活性的甾体内酯。ALW 显著抑制内皮细胞的迁移和管腔形成,这是血管生成的关键事件。使用 ALW 的体内血管生成研究表明,通过改变血清细胞因子、VEGF、GM-CSF 和 NO 水平,显著抑制了肿瘤定向毛细血管形成。ALW 治疗下调了基质金属蛋白酶(MMP)-2、MMP-9、VEGF、NF-kB 的基因表达,并上调了金属蛋白酶组织抑制剂(TIMP)-1 的表达。我们的结果表明,ALW 通过 NF-κB、VEGF、MMP-2 和 MMP-9 的基因表达抑制肿瘤特异性血管生成。本研究表明,使用 ALW 可以提供一种抑制肿瘤血管生成的有吸引力的策略。