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PMID: 10820484 Published · ppublish English Journal Article

Development of a prostate cDNA microarray and statistical gene expression analysis package.

Molecular carcinogenesis ·Vol. 28 ·No. 1 ·2000-05-00 ·Pages 12-22

Carlisle AJ, Prabhu VV, Elkahloun A, Hudson J, Trent JM, Linehan WM, Williams ED, Emmert-Buck MR, Liotta LA, Munson PJ, Krizman DB

Abstract

A cDNA microarray comprising 5184 different cDNAs spotted onto nylon membrane filters was developed for prostate gene expression studies. The clones used for arraying were identified by cluster analysis of > 35 000 prostate cDNA library-derived expressed sequence tags (ESTs) present in the dbEST database maintained by the National Center for Biotechnology Information. Total RNA from two cell lines, prostate line 8.4 and melanoma line UACC903, was used to make radiolabeled probe for filter hybridizations. The absolute intensity of each individual cDNA spot was determined by phosphorimager scanning and evaluated by a bioinformatics package developed specifically for analysis of cDNA microarray experimentation. Results indicated 89% of the genes showed intensity levels above background in prostate cells compared with only 28% in melanoma cells. Replicate probe preparations yielded results with correlation values ranging from r = 0.90 to 0.93 and coefficient of variation ranging from 16 to 28%. Findings indicate that among others, the keratin 5 and vimentin genes were differentially expressed between these two divergent cell lines. Follow-up northern blot analysis verified these two expression changes, thereby demonstrating the reliability of this system. We report the development of a cDNA microarray system that is sensitive and reliable, demonstrates a low degree of variability, and is capable of determining verifiable gene expression differences between two distinct human cell lines. This system will prove useful for differential gene expression analysis in prostate-derived cells and tissue.

MeSH Terms
DNA, Complementary/genetics,isolation & purification Gene Expression Profiling Gene Expression Regulation, Neoplastic Humans Male Oligonucleotide Array Sequence Analysis/methods Prostate Prostatic Neoplasms/genetics
Chemicals
DNA, Complementary
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Carlisle A J
Laboratory of Pathology, National Cancer Institute, Rockville, Maryland, USA.
Prabhu V V
Elkahloun A
Hudson J
Trent J M
Linehan W M
Williams E D
Emmert-Buck M R
Liotta L A
Munson P J
Krizman D B
Article Info
Journal
Molecular carcinogenesis
Abbr.
Mol Carcinog
ISSN
0899-1987
Published
2000-05-00
Pages
12-22
Language
English
Region
United States
NLM ID
8811105
Subset
IM
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