Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling by array of prostate from mice at different stages of JOCK1 prostate cancer progression to identify FGFR1-mediated gene expression changes


ABSTRACT: FGFR1 mediated changes in gene expression at different stages of JOCK1 prostate cancer progression JOCK1 mice which express a prostate localize inducible version of the FGFR1 gene (iFGFR1) were used to determine what are the changes in gene expression at distinct stages of JOCK1 tumor progression. Activation of iFGFR1 is mediated by biweekly treatements of JOCK1 mice with AP20187 (50mg/kg). Wild type mice were treated for 24 hours with CID as a control, while JOCK1 were treated with CID for 4, 12, 24 and 52 weeks. All these treatments began at 12 weeks of age. After treatment mouse prostates (ventral and dorso-lateral prostate lobes), were dissected, placed in RNAlater and incubated at -800C. Tissue was thawed and placed in TRIzol (Invitrogen) for RNA isolation according to the manufacture. Once RNA was removed, a RNA cleaning step was performed using Qiagen RNEasy columns as described by the manufacturer. Time points were performed in triplicate and each array represents a single prostate. Labeling and hybridization to the mouse Affymetrix gene array 430 2.0 was performed by the Baylor College of Medicine microarray core. All hybridizations were performed at the same time.

ORGANISM(S): Mus musculus

DISEASE(S): prostate cancer

SUBMITTER: Victor Acevedo 

PROVIDER: E-MEXP-1296 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Inducible FGFR-1 activation leads to irreversible prostate adenocarcinoma and an epithelial-to-mesenchymal transition.

Acevedo Victor D VD   Gangula Rama D RD   Freeman Kevin W KW   Li Rile R   Zhang Youngyou Y   Wang Fen F   Ayala Gustavo E GE   Peterson Leif E LE   Ittmann Michael M   Spencer David M DM  

Cancer cell 20071201 6


Fibroblast Growth Factor Receptor-1 (FGFR1) is commonly overexpressed in advanced prostate cancer (PCa). To investigate causality, we utilized an inducible FGFR1 (iFGFR1) prostate mouse model. Activation of iFGFR1 with chemical inducers of dimerization (CID) led to highly synchronous, step-wise progression to adenocarcinoma that is linked to an epithelial-to-mesenchymal transition (EMT). iFGFR1 inactivation by CID withdrawal led to full reversion of prostatic intraepithelial neoplasia, whereas P  ...[more]

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