Basic Research
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 15, 2003; 9(4): 818-823
Published online Apr 15, 2003. doi: 10.3748/wjg.v9.i4.818
Analysis of gene expression profile of pancreatic carcinoma using cDNA microarray
Zhi-Jun Tan, Xian-Gui Hu, Gui-Song Cao, Yan Tang
Zhi-Jun Tan, Xian-Gui Hu, Gui-Song Cao, Yan Tang, Department of General Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Xian-Gui Hu, Department of General Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China. hxgchw@sh163.net
Telephone: +86-21-25070571 Fax: +86-21-25070571
Received: November 6, 2002
Revised: December 1, 2002
Accepted: December 7, 2002
Published online: April 15, 2003
Abstract

AIM: To identify new diagnostic markers and drug targets, the gene expression profiles of pancreatic cancer were compared with that of adjacent normal tissues utilizing cDNA microarray analysis.

METHODS: cDNA probes were prepared by labeling mRNA from samples of six pancreatic carcinoma tissues with Cy5-dUTP and mRNA from adjacent normal tissues with Cy3-dUTP respectively through reverse transcription. The mixed probes of each sample were then hybridized with 12800 cDNA arrays (12648 unique human cDNA sequences), and the fluorescent signals were scanned by ScanArray 3000 scanner (General Scanning, Inc.). The values of Cy5-dUTP and Cy3-dUTP on each spot were analyzed and calculated by ImaGene 3.0 software (BioDiscovery, Inc.). Differentially expressed genes were screened according to the criterion that the absolute value of natural logarithm of the ratio of Cy5-dUTP to Cy3-dUTP was greater-than 0.69.

RESULTS: Among 6 samples investigated, 301 genes, which accounted for 2.38% of genes on the microarry slides, exhibited differentially expression at least in 5. There were 166 over-expressed genes including 136 having been registered in Genebank, and 135 under-expressed genes including 79 in Genebank in cancerous tissues.

CONCLUSION: Microarray analysis may provide invaluable information on disease pathology, progression, resistance to treatment, and response to cellular microenvironments of pancreatic carcinoma and ultimately may lead to improving early diagnosis and discovering innovative therapeutic approaches for cancer.

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