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消岩汤对A549/DDP细胞自噬及耐药蛋白的影响研究
引用本文:杨佩颖,许文婷,刘宏根,张欣,张莹,于晓宇,贾英杰.消岩汤对A549/DDP细胞自噬及耐药蛋白的影响研究[J].天津中医药,2016,33(6):358-362.
作者姓名:杨佩颖  许文婷  刘宏根  张欣  张莹  于晓宇  贾英杰
作者单位:天津中医药大学第一附属医院, 天津 300193,天津中医药大学第一附属医院, 天津 300193,天津中医药大学第一附属医院, 天津 300193,天津中医药大学第一附属医院, 天津 300193,天津中医药大学第一附属医院, 天津 300193,天津中医药大学第一附属医院, 天津 300193,天津中医药大学第一附属医院, 天津 300193
基金项目:国家自然科学基金资助项目(81273937),天津市科委自然科学基金青年项目(13JCQNJC10900),天津市抗癌重大专项攻关计划(12ZCDZSY15800).
摘    要:目的]通过消岩汤对耐顺铂人肺腺癌细胞A549/DDP多药耐药及自噬蛋白的影响,探究消岩汤对耐顺铂人肺腺癌A549/DDP的耐药逆转作用及探讨相关分子通路。方法]建立稳定细胞耐药模型,连续灌胃不同浓度消岩汤10 d后,通过血清药理学的实验方法,提取药物血清,用含药血清作用于肺腺癌细胞耐药细胞A549/DDP,通过实时荧光定量逆转录聚合酶链反应(QPT-PCR)和蛋白免疫印迹法(Werstern Blot)检测A549/DDP耐药、自噬相关基因的表达及相关通路蛋白的变化。结果]高剂量消岩汤,低剂量消岩汤和生理盐水作用于肺腺癌耐药细胞A549/DDP,检测A549/DDP细胞中耐药相关蛋白P-糖蛋白(P-gp)、肺抗药性相关蛋白(LRP)及自噬相关蛋白Beclin1,HMGB1m RNA和蛋白表达变化,发现高剂量组消岩汤处理细胞株后P-gp、LRP及自噬相关蛋白Beclin1,HMGB1 m RNA和蛋白均发生降低(P0.05),进一步发现消岩汤可影响AKT1-m TOR相关基因,消岩汤明显降低AKT1,m TOR蛋白的表达。结论]消岩汤通过影响AKT1-m TOR分子通路进而影响耐药相关蛋白P-gp、LRP及自噬相关蛋白Beclin1,HMGB1基因的变化。

关 键 词:消岩汤  细胞自噬  耐药  分子通路
收稿时间:2016/1/16 0:00:00

Study on the autophagy and resistance protein affected by Xiaoyan decoction in A549/DDP cells
YANG Pei-ying,XU Wen-ting,LIU Hong-gen,ZHANG Xin,ZHANG Ying,YU Xiao-yu and JIA Ying-jie.Study on the autophagy and resistance protein affected by Xiaoyan decoction in A549/DDP cells[J].Tianjin Journal of Traditional Chin Medicine,2016,33(6):358-362.
Authors:YANG Pei-ying  XU Wen-ting  LIU Hong-gen  ZHANG Xin  ZHANG Ying  YU Xiao-yu and JIA Ying-jie
Institution:The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China,The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China,The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China,The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China,The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China,The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China and The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China
Abstract:Objective] Through the cisplatin resistance of the human lung adenocarcinoma cells A549/DDP multi-resistant and influence of autophagy protein by Xiaoyan decoction, finding out the influence of elimination of cisplatin resistance of lung adenocarcinoma A549/DDP resistance reversal agents and explore relevant molecular pathways. Methods] Establish a stable cell resistance model, continuous lavaging Xiaoyan decoction with different concentrations in 10 days, by serum pharmacology experiment method with drug-containing serum on lung adenocarcinoma cells resistant cells A549/DDP, through the QRT-PCR and Werstern Blot western Blot method to detect A549/DDP resistant, autophagy protein expression of related genes and related pathways. Results] Resistance effect on lung adenocarcinoma cells A549/DDP with high dose Xiaoyan decoction, low dose Xiaoyan Decoction and normal saline, elimination saline resistance effect on lung adenocarcinoma cells A549/DDP, detecting drug-resistant related proteins in A549/DDP cell P-gp, LRP and Beclin1 protein involved in autophagy, HMGB1mRNA and protein expression changes,through the detection of A549/DDP cells drug-resistant related proteins P-gp, LRP and Beclin1 protein involved in autophagy, HMGB1mRNA and protein expression changes, high dose group of rock soup elimination processing cell lines after P-gp, LRP and Beclin1 protein involved in autophagy, both the HMGB1 mRNA and protein were lower (P<0.05). Further found that Xiaoyan decoction can affect the AKT1-elimination mTOR related genes and significantly reduce the AKT1, mTOR protein expression. Conclusion] We hypothesized that Xiaoyan decoction influence elimination drug-resistant related proteins P-gp, LRP and Beclin1 protein involved in autophagy, HMGB1 genetic changes by AKT1- mTOR molecular pathways.
Keywords:Xiaoyan decoction  autophagy  resistance  molecular pathway
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