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雷公藤甲素对人结肠癌HCT116细胞增殖、自噬和凋亡的影响

赵林 吴鹏 章平贵 谢大泽 高典 周南进

中国药理学通报2016,Vol.32Issue(10):1399-1403,1404,6.
中国药理学通报2016,Vol.32Issue(10):1399-1403,1404,6.DOI:10.3969/j.issn.1001-1978.2016.10.014

雷公藤甲素对人结肠癌HCT116细胞增殖、自噬和凋亡的影响

Effect of triptolide on human colorectal cancer HCT116 cell proliferation, autophagy and apoptosis

赵林 1吴鹏 2章平贵 2谢大泽 2高典 3周南进2

作者信息

  • 1. 江西省医学科学院实验中心,江西 南昌 330006
  • 2. 江西省医学科学院分子医学研究所,江西 南昌 330006
  • 3. 南昌大学基础医学院,江西 南昌 330006
  • 折叠

摘要

Abstract

Aim To investigate the effect of triptolide ( TP) on human colorectal cancer HCT116 cell prolif-eration and explore the potential mechanism of TP in treating colon cancer. Methods MTT assay was used for estimating the survival rates of HCT116 cells ex-posed to different concentrations and different duration time of TP. Western blot ( WB ) was used for testing the expression of LC3-Ⅱ. MDC staining was employed to detect cell autophagy. Flow cytometry ( FCM) was applied to test the effects of TP on cell apoptosis. Re-sults TP could inhibit cell proliferation in HCT116 cells. The expression of LC3-Ⅱwas enhanced with the increase of the concentration of TP after exposed to dif-ferent concentrations of TP for 48 h and the duration time of TP after exposed to 40 nmol·L-1 TP,and the number of acid autophagic vacuoles in HCT116 cells had increased, which was observed by fluorescence mi-croscope. The HCT116 cells apoptotic rates in TP group had decreased compared to control group and de-creased significantly compared to TP +3-MA group. The HCT116 cells apoptotic rates in TP group had in-creased compared to control group and increased signif-icantly compared to TP+RAPA group. Conclusion TP could inhibit the proliferation of human colon canc-er HCT116 cells and induce apoptosis in HCT116 cells, which indicates that synergy may exist between autophagy and apoptosis.

关键词

雷公藤甲素/结肠癌/HCT116细胞/增殖/自噬/凋亡

Key words

triptolide/colon cancer/HCT116 cell/proliferation/autophagy/apoptosis

分类

医药卫生

引用本文复制引用

赵林,吴鹏,章平贵,谢大泽,高典,周南进..雷公藤甲素对人结肠癌HCT116细胞增殖、自噬和凋亡的影响[J].中国药理学通报,2016,32(10):1399-1403,1404,6.

基金项目

江西省自然科学基金资助项目(No 20142BAB205079) (No 20142BAB205079)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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