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Home › Dataset Library › Identification of an SRF- and androgen-dependent gene signature in prostate cancer

Dataset: Identification of an SRF- and androgen-dependent gene signature in prostate cancer

The androgen receptor (AR) is the principal target for treatment of non-organ confined prostate cancer (PCa). Systems and bioinformatics...

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The androgen receptor (AR) is the principal target for treatment of non-organ confined prostate cancer (PCa). Systems and bioinformatics approaches suggest that considerable variation exists in the mechanisms by which AR regulates expression of effector genes and point towards a role for secondary transcription factors (TFs) therein. We identified a novel indirect mechanism of androgen action in which effects of androgens on PCa cells are mediated by Serum Response Factor (SRF). To identify and characterize genes and cellular processes that are androgen-regulated in an SRF-dependent manner in PCa, Affymetrix HG-U133 Plus 2.0 GeneChip Array analysis was performed starting from RNA obtained from LNCaP cells in which androgen stimulation was combined with siRNA-mediated SRF silencing. To this end, LNCaP cells were seeded in 60 mm dishes at a density of 550,000 cells per dish in antibiotic-free medium. The next day, cells were transfected with siGenome SmartPool siRNA targeting SRF (Dharmacon, Lafayette, CO) or a custom-made control SmartPool targeting luciferase (LUC condition) using Lipofectamine 2000 (Invitrogen, Carlsbad, CA) following the manufacturer’s instructions. Forty-two hours after transfection, cells were treated with 5nM R1881 or ethanol vehicle. 3 biological triplicates were included per treatment group. Forty-eight hours later, cells were harvested in Trizol reagent (Invitrogen). RNA was isolated, purified on RNeasy columns (Qiagen, Germantown, MD) and checked for integrity by Agilent testing (Affymetrix, Santa Clara, CA). cDNA was generated and hybridized to Human Genome U133 Plus 2.0 arrays (Affymetrix) according to the manufacturer’s instructions at the Mayo Clinic Advanced Genomics Technology Microarray Shared Resource core facility. Two-factor factorial design with three biological replicates (12 total samples) using LNCaP or SRF Silenced cells treated with either R1881 or ethanol vehicle.

Species:
human

Samples:
12

Source:
E-GEOD-22606

PubMed:
21324924

Updated:
Dec.12, 2014

Registered:
Sep.15, 2014


Factors: (via ArrayExpress)
Sample AGENT TREATMENT SIRNA TRANSFECTION PROTOCOL
GSM560828 EtOH vehicle control siRNA
GSM560828 EtOH vehicle control siRNA
GSM560828 EtOH vehicle control siRNA
GSM56083 R1881 control siRNA
GSM56083 R1881 control siRNA
GSM56083 R1881 control siRNA
GSM560834 EtOH vehicle SRF Silencing
GSM560834 EtOH vehicle SRF Silencing
GSM560834 EtOH vehicle SRF Silencing
GSM560837 R1881 SRF Silencing
GSM560837 R1881 SRF Silencing
GSM560837 R1881 SRF Silencing

Tags

  • androgen
  • cancer
  • dish
  • genome
  • organ
  • pca
  • point
  • prostate
  • prostate cancer
  • serum

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