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首页|期刊导航|医学分子生物学杂志|柴胡皂苷D通过下调miR-517a调节胶质瘤细胞体外和体内移植瘤生长

柴胡皂苷D通过下调miR-517a调节胶质瘤细胞体外和体内移植瘤生长

徐敬轩 杨岩 张勖 郭正 栾新平

医学分子生物学杂志2020,Vol.17Issue(1):33-39,7.
医学分子生物学杂志2020,Vol.17Issue(1):33-39,7.DOI:10.3870/j.issn.1672-8009.2019.01.006

柴胡皂苷D通过下调miR-517a调节胶质瘤细胞体外和体内移植瘤生长

Saikosaponin D Regulates Growth of Glioma Cells in vitro and Trans-planted Tumor in vivo by Down-regulating miR-517a

徐敬轩 1杨岩 1张勖 1郭正 1栾新平1

作者信息

  • 1. 新疆医科大学第二附属医院神经外科 乌鲁木齐市, 830028
  • 折叠

摘要

Abstract

Objective To investigate the effect of Saikosaponin D on the growth of glioma cells in vitro and in vivo by regulating miR-517a.Methods Survival rates of U-87 cells and normal astro-cytes were determined by MTT kit.miR-517a expression was detected by q-PCR.Cell apoptosis was assessed by flow cytometry.Transwell assay was applied to detect cell migration and invasion.CCK-8 kit was used to detect cell proliferation.Cleaved caspase-3, Ki67, MMP-2 and Cyclin D1 protein levels were detected by Western blotting.The model of transplanted tumor in nude mice was estab-lished and the weight of tumor in each group was detected.The expression levels of Ki67 and VEGF were detected by immunohistochemistry.Results Saikosaponin D had no effect on the survival rate of normal astrocytes, decreased the survival rate of U-87 cells, down-regulated the expression of miR-517a, promoted apoptosis, up-regulated cleaved caspase-3 protein expression, inhibited cell migration, invasion and proliferation, and down-regulated MMP-2, Cyclin D1 and Ki67 protein expression.The growth of transplanted tumor was inhibited, and the positive expression rates of Ki67 and VEGF were de-creased by Saikosaponin D.Conclusion This study shows that Saikosaponin D can down-regulate miR-517a to regulate the growth of glioma cells in vitro and transplanted tumor in vivo.

关键词

柴胡皂苷D/ 胶质瘤/ miR-517a/ 血管内皮生长因子

Key words

SaikosaponinD/glioma/miR-517a/VEGF

分类

医药卫生

引用本文复制引用

徐敬轩,杨岩,张勖,郭正,栾新平..柴胡皂苷D通过下调miR-517a调节胶质瘤细胞体外和体内移植瘤生长[J].医学分子生物学杂志,2020,17(1):33-39,7.

基金项目

资助项目:新疆维吾尔自治区自然科学基金(No.2019001C234) This work was supported by a grant from the Nature Science Foundation of Xinjiang Uygur Autonomous Region(No.2019001C234) (No.2019001C234)

医学分子生物学杂志

OACSTPCD

1672-8009

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