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As2O3联合γ分泌酶抑制剂MW167对人肝癌HepG2/ADM细胞耐药性的影响

杨莉 王雪雯 周明 张帆

吉林大学学报(医学版)2018,Vol.44Issue(1):1-7,7.
吉林大学学报(医学版)2018,Vol.44Issue(1):1-7,7.DOI:10.13481/j.1671-587x.20180101

As2O3联合γ分泌酶抑制剂MW167对人肝癌HepG2/ADM细胞耐药性的影响

Effect of arsenic trioxide combined with γ-secretase inhibitor MW167 on drug resistance of human hepatocellular carcinoma HepG2/ADM cells

杨莉 1王雪雯 2周明 1张帆2

作者信息

  • 1. 石河子大学医学院新疆地方病与民族高发病教育部重点实验室,新疆石河子832002
  • 2. 石河子大学医学院病理生理学教研室,新疆石河子832002
  • 折叠

摘要

Abstract

Objective:To investigate the influence of arsenic troxide (As2 O3) and γ-secretase inhibitor MW167used alone or in combination in the drug resistance of HepG/ADM cells,and to clarify its mechanisms.Methods:The HepG2/ADM cells were treated with different concentrations of As2 O3 (0.25,0.50,1.00,2.00,4.00,8.00mg· L-1) andMW167 (10,20,40μmol· L-1) for 24,48 and 72h,and MTT method was used to detect the optical density (A) values,then the inhibitory rates of proliferation were calculated and the drug concentration and treatment time were confirmed.The HepG2/ADM cells were divided into blank group,As2O3group,MW167 group and combination group;the non-cytotoxic doses of As2 O3 and MW167 according to the results of MTT were chosen and the HepG2/ADM cells were intervened for 48 h;the apoptotic rates were detected by FCM;RT-PCR and Western blotting methods were employed to detect the mRNA and protein expression levels of Notch-1,Hes-1,MDR-1 (P-gp),Bcl-2 and Bax in the cells in various groups.Results:At the same concentration,the inhibitory rates of proliferation of HepG2/ADM cells were enhanced with the prolongation of the treatment time of As2O3 and MW167 (P<0.05 or P<0.01);at the same time point,the inhibitory rates of proliferation of As2O3 and MW167 in the HepG2/ADM cells were increased with the increasing of drug concentration (P<0.05);the non-toxic doses of As2O3 and MW167 were 0.25 mg · L-1 and 10 μmol · L 1 and the intervention time was 48 h.After treatment for 48 h,compared with blank group,the apoptotic rates in various intervention groups were increased (P<0.05),especially in combination group (P<0.01);the expression levels of Notch-1,Hes-1,MDR-1 (P-gp),Bcl-2 mRNA and protein in various intervention groups were lower than those in blank group (P<0.05),especially in combination group (P<0.01);compared with blank group,the expression levels of Bax mRNA and protein in various intervention groups were increased (P<0.05),especially in combination group (P<0.01).Conclusion:As2 O3 can reverse the drug resistance of HepG2/ADM cells,its mechanism may be related to inhibition of cell proliferation,promotion of apoptosis,down-regulation of the expression levels of Notch-1,Hes-1,MDR (P-gp),Bcl-2 and up-regulation of the expression levels of Bax mRNA and protein.

关键词

三氧化二砷/肝肿瘤/Notch信号通路/多药耐药/细胞凋亡/细胞增殖

Key words

arsenic trioxide/liver neoplasms/Notch signaling pathway/multidrug resistance/apoptosis/cell proliferation

分类

医药卫生

引用本文复制引用

杨莉,王雪雯,周明,张帆..As2O3联合γ分泌酶抑制剂MW167对人肝癌HepG2/ADM细胞耐药性的影响[J].吉林大学学报(医学版),2018,44(1):1-7,7.

基金项目

国家自然科学基金资助课题(81060174) (81060174)

吉林大学学报(医学版)

OA北大核心CSCDCSTPCD

1671-587X

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