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冬凌草甲素对人前列腺癌细胞系PC3增殖、凋亡和侵袭的调节作用

LIU Shaoyong YOU Lu WANG Wei ZHAI Changming

医学分子生物学杂志2019,Vol.16Issue(1):19-23,5.
医学分子生物学杂志2019,Vol.16Issue(1):19-23,5.DOI:10. 3870/j. issn. 1672-8009. 2019. 01. 004

冬凌草甲素对人前列腺癌细胞系PC3增殖、凋亡和侵袭的调节作用

Regulatory Effect of Oridonin on the Proliferation, Apoptosis and In-vasion of Prostate Cancer Cell Line PC3

LIU Shaoyong 1YOU Lu 2WANG Wei 1ZHAI Changming3

作者信息

  • 1. Cancer Hospital Affiliated to Chongqing University, Chongqing Institute of Oncology, Chongqing Cancer Hospital, Tcm Oncology, Chongqing, 400030, China
  • 2. Cancer Hospital affiliated to Chongqing University
  • 3. Beijing University of Chinese Medicine, Beijing, 100029, China
  • 折叠

摘要

Abstract

Objective To investigate the effects of oridonin on the proliferation, apoptosis and invasion of prostate cancer cell line PC3. Methods Cells were divided into PC3, oridonin (5 m mol/L) , oridonin (10 mmol/L) and Oridonin (20 mmol/L) groups and treated with orido-nin at 0, 5, 10 and 20 mmol/L. Cell viability, apoptosis and invasion ability of PC3 cells was re-spectively detected by CCK8, flow cytometry and Transwell assy. The protein levels of Ki67, Caspase-3 and vascular endothelial growth factor ( VEGF ) were measured by Western blot-ting. Results Compared with PC3 group, the proliferation times of PC3 cells in Oridonin (5, 10, 20 mmol/L) group were decreased after treatment with oridonin for 4 days and the expression of pro-liferation-related protein Ki67 was inhibited significantly. Moreover, the cell apoptosis rate in Orido-nin (5, 10, 20 mmol/L) groups was increased as compared with PC3 group, and protein level of Caspase-3 was evidently increased. In addition, Oridonin (5, 10, 20 mmol/L) decreased inva-sion of PC3 cells and inhibited the expression of VEGF.

关键词

前列腺癌/细胞增殖/细胞凋亡/侵袭

Key words

prostate cancer/proliferation/apoptosis/invasion

分类

医药卫生

引用本文复制引用

LIU Shaoyong,YOU Lu,WANG Wei,ZHAI Changming..冬凌草甲素对人前列腺癌细胞系PC3增殖、凋亡和侵袭的调节作用[J].医学分子生物学杂志,2019,16(1):19-23,5.

基金项目

重庆市自然科学基金(No.CSTC2006EB5030) (No.CSTC2006EB5030)

医学分子生物学杂志

OACSTPCD

1672-8009

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