Analyzing Gene Expression Profile in K562 Cells Exposed to Sodium Valproate Using Microarray Combined with the Connectivity Map Database

被引:56
|
作者
Zhang, Xiang-Zhong [2 ]
Yin, Ai-Hua [3 ,4 ]
Lin, Dong-Jun [2 ]
Zhu, Xiao-Yu [1 ,5 ]
Ding, Qian [1 ,6 ]
Wang, Chun-Huai [1 ]
Chen, Yun-Xian [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Hematol, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Hematol, Guangzhou 510630, Guangdong, Peoples R China
[3] Women & Children Hosp Guangdong Prov, Prenatal Diag Ctr, Guangzhou 510010, Guangdong, Peoples R China
[4] Dept Hlth Guangdong Prov Maternal & Children Meta, Key Lab, Guangzhou 510010, Guangdong, Peoples R China
[5] Anhui Med Univ, Anhui Prov Hosp, Dept Hematol, Hefei 230001, Anhui, Peoples R China
[6] Guizhou Prov Hosp, Anhui Prov Hosp, Guiyang 550002, Guizhou, Peoples R China
来源
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY | 2012年
关键词
ACUTE MYELOID-LEUKEMIA; TRANS-RETINOIC ACID; HISTONE DEACETYLASE INHIBITOR; INDUCED GROWTH ARREST; OXIDATIVE STRESS; MYELODYSPLASTIC SYNDROME; ANTILEUKEMIC ACTIVITY; KINASE-ACTIVITY; CLINICAL-TRIAL; APOPTOSIS;
D O I
10.1155/2012/654291
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To explore the mechanism underlying antileukaemia effect of sodium valproate, the growth and survival of the K562 cell line were investigated. Global profiles of gene expression in K562 cells exposed to sodium valproate were assessed and validated. The differentially expressed genes identified were further used to query the connectivity map database to retrieve a ranked list of compounds that act on the same intracellular targets as sodium valproate. A significant increase in cell apoptosis and a change in gene expression profile were observed in valproate-exposed K562 cells. The significant enrichment analysis of gene ontology terms for the differentially expressed genes showed that these genes were involved in many important biological processes. Eight differentially expressed genes involved in apoptosis were verified by quantitative real-time PCR. The connectivity map analysis showed gene expression profile in K562 cells exposed to sodium valproate was most similar to that of HDACi and PI3K inhibitors, suggesting that sodium valproate might exert antileukaemic action by inhibiting HDAC as well as inhibiting PI3K pathway. In conclusion, our data might provide clues to elucidate the molecular and therapeutic potential of VPA in leukaemia treatment, and the connectivity map is a useful tool for exploring the molecular mechanism of drug action.
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页数:8
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