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首页|期刊导航|西安交通大学学报(医学版)|ICI118551联合吉西他滨对胰腺癌细胞BxPC-3增殖和凋亡的影响及其机制

ICI118551联合吉西他滨对胰腺癌细胞BxPC-3增殖和凋亡的影响及其机制

单涛 徐军 刘江波 李军涛 李彬 段万星

西安交通大学学报(医学版)2012,Vol.33Issue(3):336-339,364,5.
西安交通大学学报(医学版)2012,Vol.33Issue(3):336-339,364,5.

ICI118551联合吉西他滨对胰腺癌细胞BxPC-3增殖和凋亡的影响及其机制

Effect and mechanisms of ICI 118551 combined with gemcitabine on the proliferation and apoptosis of BxP C-3 cells

单涛 1徐军 1刘江波 1李军涛 1李彬 1段万星1

作者信息

  • 1. 西安交通大学医学院第一附属医院肝胆外科,陕西西安710061
  • 折叠

摘要

Abstract

To investigate the anti-proliferative effects of P,-adrenoceptor blocker ICI 118551, gemcitabine and ICI 118551 + gemcitabine on BxPC-3 cells and further analyze the underlying mechanisms. Methods MTT was used to detect the anti-prolifcrativc effect of ICI 118551, gemcitabine and ICI 118551 + gemcitabine on BxPC-3 cells. The apoptosis index was determined using TUNEL, and Annexin V and fluorescein isothiocyanate/propidium iodide flow cytometry assay, respectively. Expressions of Bcl-2 and Bax mRNA were detected by RT-PCR. Protein levels of Bcl-2, Bax and NF-kB subunit P65 were analyzed by Western blotting. Results ICI 118551, gemcitabine and ICI 118551 + gemcitabine could suppress proliferation of BxPC-3 cells. ICI 118551 + gemcitabine showed a higher apoptosis rate induction than ICI 118551 or gemcitabine alone. When cells were treated with gemcitabine in combination with ICI 118551, NF-kB activation was blocked; the expression of Bax/Bcl-2 protein was substantially increased. Conclusion ICI 118551 combined with gemcitabine has a synergistic anticancer effect on BxPC-3 cells, and the combination may be an effective therapeutic strategy for pancreatic cancer.

关键词

吉西他滨/β2上腺素能受体阻滞剂/胰腺癌/凋亡/ICI 118551/增殖

Key words

gemcitabine/ β2-adrenoceptor blocker/ pancreatic cancers apoptosis/ ICI 118551/ proliferation

分类

医药卫生

引用本文复制引用

单涛,徐军,刘江波,李军涛,李彬,段万星..ICI118551联合吉西他滨对胰腺癌细胞BxPC-3增殖和凋亡的影响及其机制[J].西安交通大学学报(医学版),2012,33(3):336-339,364,5.

基金项目

陕西省13115科技攻关项目资助(No.2010ZDKG-49) (No.2010ZDKG-49)

西安交通大学学报(医学版)

OA北大核心CSCDCSTPCD

1671-8259

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