Microarray and pathway analysis of Differential Gene Expression between two kinds of prostate cancer cell lines sensitive and insensitive to docetaxel

被引:0
作者
机构
[1] Department of Microbiology and Immunology, Basic Medical College of Zhengzhou University
[2] Department of Hepatobiliary Surgery, Henan Provincial Cancer Hospital, Zhengzhou
[3] Center of Functional Experiment, Basic Medical College of Zhengzhou University
来源
Zhu, S. | 1600年 / Asian Network for Scientific Information卷 / 12期
关键词
Differential gene expression; Docetaxel; Microarray; Prostate cancer;
D O I
10.3923/itj.2013.8281.8286
中图分类号
学科分类号
摘要
Analyzing Differential Expression Gene (DEG) and identifying candidate gene in prostate cancer cell lines that were resistant to docetaxel, which might be used for the purposes of screening targeted therapy. Gene expression pro?les of the tumors from docetaxel treated mice were performed using Agilent human whole genomic oligonucleotide microarrays. The microarray data were validated and the differential expression genes were analyzed using IPA software. The prostate cancer cell lines PCS and LNCaP were sensitive to docetaxel but VcaP and CWR22 were resistant to docetaxel cell lines. It indicated that some genes up-regulated or down-regulated in docetaxel resistant cell lines may be candidate genes for targeted therapy, after evaluating by Gene Expression Microarray and signal pathway. The significantiy up-regulated genes including Bcl-11 A, EPHA4 and CX3CL1 may be the potential candidates for further investigation in docetaxel-resistant tumor cells. © 2013 Asian Network for Scientific Information.
引用
收藏
页码:8281 / 8286
页数:5
相关论文
共 13 条
[1]  
Albrecht M., Jiang W., Kumi-Diaka J., Lansky E.P., Gommersall L.M., Patel A., Mansel R.E., Neeman I., Geldof A.A., Campbell M.J., Pomegranate extracts potently suppress proliferation, xenograft growth, and invasion of human prostate cancer cells, Journal of Medicinal Food, 7, 3, pp. 274-283, (2004)
[2]  
Brasier A.R., The NF-eB regulatory network, Cardiovasc. Toxicol., 6, pp. 111-130, (2006)
[3]  
Gilmore T.D., Introduction to NF-κB: Players, pathways, perspectives, Oncogene, 25, 51, pp. 6680-6684, (2006)
[4]  
Goldshmit Y., Spanevello M.D., Tajouri S., Li L., Rogers F., Et al., EphA4 blockers promote axonal regeneration and functional recovery following spinal cord injury in mice, PloS One, 6, (2011)
[5]  
Kudo F.A., Muto A., Maloney S.P., Pimiento J.M., Bergaya S., Fitzgerald T.N., Westvik T.S., Frattini J.C., Breuer C.K., Cha C.H., Nishibe T., Tellides G., Sessa W.C., Dardik A., Venous identity is lost but arterial identity is not gained during vein graft adaptation, Arteriosclerosis, Thrombosis, and Vascular Biology, 27, 7, pp. 1562-1571, (2007)
[6]  
Mohsenzadegan M., Madjd Z., Asgari M., Abolhasani M., Shekarabi M., Taeb J., Shariftabrizi A., Reduced expression of NGEP is associated with high-grade prostate cancers: A tissue microarray analysis, Cancer Immunol. Immunotherapy, 62, pp. 1609-1618, (2013)
[7]  
Orton R.J., Sturm O.E., Vyshemirsky V., Calder M., Gilbert D.R., Kolch W., Computational modelling of the receptor-tyrosine-kinase-activated MAPK pathway, Biochemical Journal, 392, 2, pp. 249-261, (2005)
[8]  
Oshima T., Akaike M., Yoshihara K., Shiozawaand M., Yamamoto N., Et al., Overexpression ofEphA4 gene and reduced expression of EphB2 gene correlates with liver metastasis in colorectal cancer, Int. J. Oncol., 33, pp. 573-577, (2008)
[9]  
Ploussard G., Teny S., Maiue P., Uory Y.A., Sirab N., Et al., Class III [3-tubulin expression predicts prostate tumor aggressiveness and patient response to docetaxel-based chemotherapy, Cancer Res, 70, pp. 9253-6410, (2010)
[10]  
Suarez C., Morales-Barrera R., Ramos V., Nunez I., Valverde C., Et al., Role of immunotherapy in castration-resistant prostate cancer, BJU Int., (2013)