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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2010, Vol. 15 ›› Issue (3): 266-271.

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Gene expression profiles-based approach identifies candidate therapeutic compounds for lung adenocarcinoma

WANG Gui-ping1,2, YE Yun1,3, YANG Xiao-qing1, CHEN Xin-mei1, LIA NG Shuang1, ZHENG Wen-ling1, MA Wen-li1   

  1. 1Institute of Genetic Engineering, Southern Medical University, Guangzhou 510515, Guangdong, China;
    2GuangZhou Medical College, Guangzhou 510180, Guangdong, China;
    3Department of Biological and Chemical Engineering, Guangxi University of Technology, Liuzhou 545006,Guangxi,China
  • Received:2010-01-11 Revised:2010-01-11 Published:2020-10-14

Abstract: AIM: To screen the candidate therapeutic compounds for lung adeno carcinoma with gene expression profiles-based approach. METHODS: Two published microarray data (GSE7670 and GSE10072) were downloaded from Gene Expression Omnibus(GEO)web. A meta-analysis were performed with the dchips of tware, and pathway enrichment analysis was done with gene set enrichment analysis method (GSEA).Finally, candidate therapeutic compounds for lung adenocarcinoma were screened by Connectivity map analysis. RESULTS: The rewere 379 differential gene expression, including 94 up-regulated gene and 285 down-regulated gene. Pathway enrichment analy sis showed that there were 18 biological pathw aysrelated with lung adenocarcinoma. With Connectivity map analysis, We screened out eight candida te compounds, including Vorinostat, 15-delta prostaglandin J2, trichostatin A, tanespimycin, etc. In the following experiment, we demo nst rated that 15-delta prostaglandin J2 can inhibit A549 cell prolification. CONCLUSION: Our results demonstrated that gene expression profiles-based approach is perspective for screening the candidate the rapeutic compounds, which accelerates the introduction of compounds into the clinic.

Key words: Gene expression profiles, Lung adenocarcinoma, Connectivity map

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