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Home › Dataset Library › Transcription profiling of mouse prostate from wild type vs. Nkx3.1 Pten compound mutant suggests a role for AP-1 transcription factors...

Dataset: Transcription profiling of mouse prostate from wild type vs. Nkx3.1 Pten compound mutant suggests a role for AP-1 transcription factors (c-Jun, c-Fos) in prostate cancer progression and clinical outcome of prostate tumor

In our investigations of the molecular pathways of prostate tumorigenesis in Nkx3.1; Pten mutant mice using gene expression profiling, we...

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In our investigations of the molecular pathways of prostate tumorigenesis in Nkx3.1; Pten mutant mice using gene expression profiling, we now find that the AP-1 transcription factors, c-Jun and c-Fos, are significantly up-regulated during cancer progression. Forced expression of c-Fos and c-Jun in prostate cancer cells results in increased tumorigenicity, activation of Erk MAP kinase, and enhanced survival in the absence of androgens, which are hallmarks of disease progression. In humans, Jun and Fos proteins are significantly up-regulated during prostate cancer progression and significantly correlated with activation of Erk MAP kinase. Most notably, expression of Jun is associated with disease recurrence independent of other currently used prognostic indicators. These analyses reveal a hitherto unappreciated role for AP-1 transcription factors in prostate cancer progression vis-à-vis Erk MAP kinase signaling, as well as the identification of a novel marker of disease recurrence, namely c-Jun. Experiment Overall Design: Mouse prostate was collected from wild-type or the Nkx3.1; Pten compound mutant mice at the age of 8-16 months. One lobe of dosolateral prostate was snap-frozen in OCT and stored at -80ºC for laser capture microdissection (LCM). To obtain androgen-independent lesions, mice were castrated at 7 to 14 months of age. Mice were sacrificed for analysis at 8 to 16 months of age and one dosolateral prostatic lobe was snap-frozen in OCT and stored at -80ºC for LCM. Approximate 1000 Prostate epithelial cells were isolated from normal prostate, dysplasia, prostatic intraepithelial neoplasia (PIN) or cancer lesions using PixCell IIE LCM system (Arcturus), followed by RNA linear amplification and labeling using Small Sample Labeling Protocol VII (Affymetrix). Samples were labeled using a BioArray High Yield RNA transcript labeling kit (Enzo Life Scientific) and were hybridized to MOE430A GeneChips containing 22,690 well characterized mouse genes/ESTs (Affymetrix).

Species:
mouse

Samples:
26

Source:
E-GEOD-11836

Updated:
Dec.12, 2014

Registered:
Nov.24, 2014


Factors: (via ArrayExpress)
Sample
GSE11836GSM299067
GSE11836GSM299068
GSE11836GSM299069
GSE11836GSM299070
GSE11836GSM299063
GSE11836GSM299064
GSE11836GSM299065
GSE11836GSM299066
GSE11836GSM299049
GSE11836GSM299050
GSE11836GSM299051
GSE11836GSM299052
GSE11836GSM299053
GSE11836GSM299058
GSE11836GSM299059
GSE11836GSM299060
GSE11836GSM299061
GSE11836GSM299062
GSE11836GSM299054
GSE11836GSM299055
GSE11836GSM299056
GSE11836GSM299057
GSE11836GSM299045
GSE11836GSM299046
GSE11836GSM299047
GSE11836GSM299048

Tags

  • androgen
  • cancer
  • disease
  • lcm
  • prostate
  • prostate cancer

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