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首页|期刊导航|山东医药|生长抑素与吉西他滨联合应用对人转移性胰腺癌细胞株AsPC-1增殖的影响

生长抑素与吉西他滨联合应用对人转移性胰腺癌细胞株AsPC-1增殖的影响

刘力 饶奇硕 雷昌斌 王文婷 彭钊 旷星星 刘国文

山东医药2017,Vol.57Issue(47):9-12,4.
山东医药2017,Vol.57Issue(47):9-12,4.DOI:10.3969/j.issn.1002-266X.2017.47.003

生长抑素与吉西他滨联合应用对人转移性胰腺癌细胞株AsPC-1增殖的影响

Effect of somatostatin combined with gemcitabine on proliferation of human metastatic pancreatic cancer cell line AsPC-1

刘力 1饶奇硕 2雷昌斌 1王文婷 1彭钊 1旷星星 3刘国文2

作者信息

  • 1. 湘南学院附属医院,湖南郴州423000
  • 2. 南华大学附属第二医院
  • 3. 南华大学病原生物学研究所
  • 折叠

摘要

Abstract

Objective To observe the effect of combined therapy with somatostatin (SST) and gemcitabine (Gem) on the proliferation of human metastatic pancreatic cancer AsPC-1 cells.Methods The AsPC-1 cells were cultured in vitro.① The cells were treated with 0,100,200,400,600,and 800 μ,g/mL SST for 24,48,and72 h,then we calculated the IC50 of SST.② The cells were treated with 0,0.1,1 5,10,20,40,and 60 μmol/L Gem for 48 h,and we calculated the IC50 of Gem.After that,AsPC-1 cells were divided into four groups:an untreated control group (group A),a group treated with SST at IC50 (group B),a group treated with Gem at IC50 (group C),and a group treated with SST + Gem at half of their IC50 (group D).At 48 h after treatment,the inhibition rates were calculated.Results For AsPC-1 cells,IC50 of SST was 600 μg/mL at 48 h,and IC50 of Gem was 20 μmol/L.The inhibition rates in the groups A,B,C and D were 0.00% ± 3.79%,52.59% ± 4.57%,48.11% ± 10.93%,and 64.86% ± 4.83%,respectively.The cell growth was significantly inhibited in the groups B,C,and D as compared with that of group A (P < 0.05),and the inhibition rate was significantly higher in the group D than in the groups B and C (P < 0.05).Conclusion The combination of SST and Gem can inhibit the growth of AsPC-1 cells.

关键词

生长抑素/吉西他滨/转移性胰腺癌细胞AsPC-1

Key words

somatostatin/gemcitabine/metastatic pancreatic cancer cells AsPC-1

分类

医药卫生

引用本文复制引用

刘力,饶奇硕,雷昌斌,王文婷,彭钊,旷星星,刘国文..生长抑素与吉西他滨联合应用对人转移性胰腺癌细胞株AsPC-1增殖的影响[J].山东医药,2017,57(47):9-12,4.

基金项目

湖南省教育厅资助科研项目(16C1487). (16C1487)

山东医药

OACSTPCD

1002-266X

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