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应用基因芯片技术筛选胰腺癌多药耐药相关基因
引用本文:Feng B,Zhao YP,Chen G,Zhang TP,Wu YD. 应用基因芯片技术筛选胰腺癌多药耐药相关基因[J]. 中华外科杂志, 2007, 45(23): 1629-1633
作者姓名:Feng B  Zhao YP  Chen G  Zhang TP  Wu YD
作者单位:1. 中国协和医科大学,北京协和医院外科,中国医学科学院,100730
2. 中国协和医科大学,基础医学院,中国医学科学院,100730
摘    要:目的应用基因芯片技术筛选胰腺导管腺癌(PDAC)获得性多药耐药(MDR)相关基因。方法通过含人类全基因组的寡聚核苷酸基因芯片(Affymetrix HG U133 2.0plus)筛查人胰腺癌细胞株SW1990与多药耐药细胞亚株SW1990/5-FU,SW1990/ADM和SW1990/GEM之间的表达基因差异,并进行生物信息学分析。结果与亲本株SW1990相比,3株耐药细胞亚株中表达均有差异的基因共有165条;其中上调表达基因43个,下调表达基因122个。差异表达基因的功能分类包括:抗氧化还原、细胞凋亡、细胞周期、信号转导、细胞黏附相关的基因等。聚类分析发现差异基因中的PRDX4簇、TNKS2簇及CCDC5簇可能与耐药发生密切相关。结论胰腺癌对化疗的多药耐药是复杂的多基因作用的结果。本试验初步建立了胰腺癌多药耐药发生相关的总体基因表达改变图谱,为胰腺癌多药耐药发生机制的研究提供了新的靶点。

关 键 词:胰腺肿瘤  多药耐药  基因芯片  差异表达基因  聚类分析

Selection of genes related to multidrug resistance of pancreatic ductal adenocarcinoma by microarray analysis
Feng Bin,Zhao Yu-pei,Chen Ge,Zhang Tai-ping,Wu Yuan-de. Selection of genes related to multidrug resistance of pancreatic ductal adenocarcinoma by microarray analysis[J]. Chinese Journal of Surgery, 2007, 45(23): 1629-1633
Authors:Feng Bin  Zhao Yu-pei  Chen Ge  Zhang Tai-ping  Wu Yuan-de
Affiliation:Department of Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Science, Beijing, China.
Abstract:OBJECTIVE: To investigate the genes concerning multidrug resistance (MDR) of pancreatic ductal adenocarcinoma with microarray analysis. METHODS: Gene expression profile of pancreatic cancer cell line SW1990 and resistance subline SW1990/5-FU, SW1990/ADM, SW1990/GEM were screened in two independent replicates using oligonucleotide microarray (Affymetrix HG U133 2.0 plus) which contained 38,500 human genes. And advanced bioinformatics analysis was conducted. RESULTS: Totally, 165 genes and expressed sequence tags (ESTs), which were seldom reported to be related with drug resistance before,were statistically difference and the fold change was up- or down-regulated at least 2 folds in all 3 resistant sub-lines when compared with SW1990. According gene ontology, the genes related to oxidoreductase activity, apoptosis, cell cycle, signal transduction and cell adhesion might be some epigenetic changes for MDR development. Hierarchical clustering analysis, showed several interesting clusters, namely, TNKS2, PRDX4 and CCDC4. CONCLUSIONS: MDR of pancreatic cancer is a complicated and multifactorial process. In the present study, a widespread differential gene expression pattern was constructed in PDAC multidrug resistant cells. Advanced study will provide new targets for MDR research and cast insights into research of the molecular mechanism of MDR.
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