蝎毒多肽提取物对白血病细胞株K562/A02荷瘤鼠耐药性的影响

目的探讨蝎毒多肽(peptide extract from scorpion venom,PESV)逆转白血病干细胞(leukemia stem cells,LSC)在体内多药耐药(multidrug resistance,MDR)的分子机制。方法以多药耐药的K562/A02细胞株成模白血病BALB/c裸鼠为例,成模鼠随机分为6组:模型对照组、阿霉素(ADM)组、PESV组、ADM+PESV(H)组、ADM+PESV(M)组、ADM+PESV(L)组。模型对照组给予等体积0.9%氯化钠溶液腹腔注射,其余各组予相应剂量ADM和(或)PESV腹腔注射,连续给药14天。第21天观察各组裸鼠移植瘤生长...

Full description

Saved in:
Bibliographic Details
Published in肿瘤防治研究 Vol. 43; no. 3; pp. 181 - 187
Main Author 杨向东 杨文华 刘宝山 伊学军 高宏 姚芳 王兴丽 闫理想
Format Journal Article
LanguageChinese
Published 2016
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:目的探讨蝎毒多肽(peptide extract from scorpion venom,PESV)逆转白血病干细胞(leukemia stem cells,LSC)在体内多药耐药(multidrug resistance,MDR)的分子机制。方法以多药耐药的K562/A02细胞株成模白血病BALB/c裸鼠为例,成模鼠随机分为6组:模型对照组、阿霉素(ADM)组、PESV组、ADM+PESV(H)组、ADM+PESV(M)组、ADM+PESV(L)组。模型对照组给予等体积0.9%氯化钠溶液腹腔注射,其余各组予相应剂量ADM和(或)PESV腹腔注射,连续给药14天。第21天观察各组裸鼠移植瘤生长情况,分别检测瘤块中LSC:细胞膜上P-gp的表达,细胞质中ALDH、PI3K的变化及细胞核中MDR1、NF-κB的活性。结果 K562/A02细胞经免疫磁珠分选前后的CD34+CD38-细胞比率和IC50值分别为31.5%、(60.33±10.68)μg/ml和92.8%、(58.33±9.72)μg/ml,分选后细胞干性显著提高,而耐药性无差异性损失;各组造模裸鼠成瘤率100%。瘤体中LSC:流式细胞仪检测细胞膜上P-gp表达结果:检测对照组89.8%、ADM组91.9%、PESV组88.4%、ADM+PESV(H)组53.9%、ADM+PESV(M)组78.0%、ADM+PESV(L)组78.7%;半定量RT-PCR检测MDR1 m RNA的表达:PESV组〉ADM+PESV(L)组〉ADM+PESV(M)组〉ADM+PESV(H)组〉ADM组;免疫组织化学检测ALDH,显示灰度值ADM组〉PESV组〉ADM+PESV(H)组〉ADM+PESV(M)组〉ADM+PESV(L)组;Western blot检测PI3K分子与Elisa检测NF-κB因子结果一致,在ADM组、PESV组表达上调,在ADM+PESV组中表达下调,下调强度与PESV剂量呈正相关。结论 PESV具有下调白血病干细胞膜上P-gp,细胞质内ALDH、PI3K及细胞核中MDR1、NF-κB的表达水平,增强了白血病K562/A02干细胞在体内对ADM的敏感度,逆转其多药耐药特性。
Bibliography:42-1241/R
YANG Xiangdong, YANG Wenhua, LIU Baoshan, YI Xuejun, GAO Hong, YAO Fang, WANG Xingli, YAN Lixiang( 1. Hematology Department, The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300381, China; 2. Traditional Chinese Medicine Department, General Hospital Affiliated to Tianjin Medical University, Tianjin 300052, China; 3. Postgraduate School, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China)
Leukemia; Peptide extract from scorpion venom(PESV); K562/A02; BALB/c nude mice; Multidrug resistance(MDR); Reversion
Objective To investigate the molecular mechanism of the reversion impact of peptide extract from scorpion venom(PESV) on multidrug resistance(MDR) of leukemia stem cells(LSC) in vivo. Methods Took leukemia BALB/c nude mice modeled by K562/A02 cell line for example, they were randomly divided into six groups: Model control group, ADM group, PESV group, ADM+PESV high-dose(H) group, ADM+PESV middle-dose(M) group, and ADM+PESV low-dose(L) gr
ISSN:1000-8578