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莪术醇诱导胆管癌细胞凋亡和调控细胞周期的体外研究

张金铎 苏刚 逯娅雯 周昕玥 赵盛 把永江 唐增伟 孟文勃 李汛

兰州大学学报(医学版)2018,Vol.44Issue(1):65-70,6.
兰州大学学报(医学版)2018,Vol.44Issue(1):65-70,6.DOI:10.13885/j.issn.1000-2812.2018.01.012

莪术醇诱导胆管癌细胞凋亡和调控细胞周期的体外研究

The Study on the apoptosis effect and cell cycle regulation of curcumol on cholangiacarcinoma cell line in vitro

张金铎 1苏刚 2逯娅雯 3周昕玥 4赵盛 3把永江 1唐增伟 3孟文勃 5李汛1

作者信息

  • 1. 兰州大学第一临床医学院,甘肃兰州730000
  • 2. 兰州大学第一医院特需外科,甘肃兰州730000
  • 3. 兰州大学基础医学院遗传学研究所甘肃兰州730000
  • 4. 兰州大学第一医院东岗院区甘肃省生物治疗与再生医学重点实验室,甘肃兰州730000
  • 5. 福建医科大学临床医学部,福建福州350122
  • 折叠

摘要

Abstract

Objective To observe the effect of curcumol on the proliferation and apoptosis of intrahepatic cholangiocarcinoma RBE cells in vitro and explore its possible mechanisms.Methods The inhibitory effect of curcumol on RBE cells was estimated with XTT assay,and different action times (24,48,72 h) and curcumol concertrations (12.5,25,50,75,100 μg/mL) were adopted.Caspase-3/7 activity was determined by microplate reader.Alteration of cell cycle and apoptosis rate were detected by flow cytometry and the expression of Cyclin D1,NF-κB,and Bcl-2 were measured with Western Blot.Results Curcumol had remarkably inhibitory effects on the proliferation of RBE cells and was in a concentration-and time-dependent manner within certain range (50-100 μg/mL).After treatment with curcumol for 48 hours,the activity levels of Caspase-3/7 significantly increased and this could induce RBE cells arrest in G1 phase with the expression level of Cyclin D1 being increased,while the NF-κB,Bcl-2 levels were decreased.Conclusion Curcumol could moderately inhibit the proliferation of RBE cells and induce G1 arrest of cell cycle and induce cell apoptosis via mitochondrial pathways.

关键词

莪术醇/胆管癌/细胞周期/凋亡

Key words

curcumol/cholangiocarcinoma/cell cycle/apoptosis

分类

医药卫生

引用本文复制引用

张金铎,苏刚,逯娅雯,周昕玥,赵盛,把永江,唐增伟,孟文勃,李汛..莪术醇诱导胆管癌细胞凋亡和调控细胞周期的体外研究[J].兰州大学学报(医学版),2018,44(1):65-70,6.

基金项目

“西部之光”人才培养引进计划项目(科发人函字(2015)90号) (科发人函字(2015)

甘肃省中医药管理局科研项目(GZK-2015-69) (GZK-2015-69)

甘肃省自然科学基金项目(17JR5RA273) (17JR5RA273)

兰州大学学报(医学版)

OACSTPCD

2097-681X

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