Abstract |
In prostate cancer progression, the basal lamina switches from predominantly laminin-5 to laminin-10. DU-145 prostate cancer cells were treated with either soluble laminin-5 (20 ng/ml) or laminin-10 (1 microg/ml) for 6, 24, and 48 hr. Total RNA was harvested for a 7,500 human cDNA microarray. Hybridizations were carried out in accordance with a 10 sample analysis of variance (ANOVA) statistical model. One thousand one hundred sixteen genes had measurable expression 2 standard deviations above background and 50% of spots for any given sample for all hybridizations were positive. Expression values of significantly varying genes were clustered and a list of 408 genes (P < 0.05) with a 1.5 or greater fold change in at least one time point were chosen for further analysis. Seventy eight changed in a time-dependent manner with laminin-10 treatment, 85 changed with laminin-5, and 13 showed changes with both treatments. The 408 genes that passed a paired t-test in at least one time-dependent category were further analyzed using Pathway Miner. One of the largest gene association networks involved signal transduction in the growth factor-MAP kinase pathways. EGFR was validated by real-time PCR and laminin-10 mediated cell adhesion activated EGFR in DU-145 cells. Both laminins appear to be important signal transducers in prostate cancer.
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Authors | Robert Calaluce, Shaleen K Beck, Elisabeth L Bair, Ritu Pandey, Kevin A Greer, Adam M Hoying, James B Hoying, David W Mount, Raymond B Nagle |
Journal | The Prostate
(Prostate)
Vol. 66
Issue 13
Pg. 1381-90
(Sep 15 2006)
ISSN: 0270-4137 [Print] United States |
PMID | 16804886
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Cell Adhesion Molecules
- DNA, Neoplasm
- Laminin
- RNA, Neoplasm
- kalinin
- laminin 10
- ErbB Receptors
- Calpain
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Topics |
- Calpain
(genetics, metabolism)
- Cell Adhesion Molecules
(physiology)
- Cell Line, Tumor
- DNA, Neoplasm
(genetics)
- ErbB Receptors
(genetics, metabolism)
- Gene Expression Profiling
- Gene Expression Regulation, Neoplastic
(drug effects, genetics)
- Humans
- Laminin
(physiology)
- MAP Kinase Signaling System
(genetics)
- Male
- Oligonucleotide Array Sequence Analysis
- Prostatic Neoplasms
(genetics, metabolism, pathology)
- RNA, Neoplasm
(genetics)
- Signal Transduction
(genetics)
- Time Factors
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