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Vitamin D receptor activation reduces VCaP xenograft tumor growth and counteracts ERG activity despite induction of TMPRSS2:ERG.

Abstract
Whether vitamin D is chemopreventive and/or has potential therapeutically in prostate cancer is unresolved. One confounding factor is that many prostate cancers express a TMPRSS2:ERG fusion gene whose expression is increased both by androgens and by vitamin D receptor (VDR) activation. Two challenges that limit VDR agonist use clinically are hypercalcemia and the cooperation of VDR with ERG to hyper-induce the 1α,25-dihydroxyvitamin D3 metabolizing enzyme, CYP24A1, thus reducing VDR activity. Using the VCaP TMPRSS2:ERG positive cell line as a model, we found that a nonsecosteroidal CYP24A1 resistant VDR agonist, VDRM2, substantially reduces growth of xenograft tumors without inducing hypercalcemia. Utilizing next generation RNA sequencing, we found a very high overlap of 1,25D(OH)2D3 and VDRM2 regulated genes and by drawing upon previously published datasets to create an ERG signature, we found activation of VDR does not induce ERG activity above the already high basal levels present in VCaP cells. Moreover, we found VDR activation opposes 8 of the 10 most significant ERG regulated Hallmark gene set collection pathways from Gene Set Enrichment Analysis (GSEA). Thus, a CYP24A1 resistant VDR agonist may be beneficial for treatment of TMPRSS2:ERG positive prostate cancer; one negative consequence of TMPRSS2:ERG expression is inactivation of VDR signaling.
AuthorsJustin M Roberts, Rebeca San Martin, D Badrajee Piyarathna, James G MacKrell, Guilherme V Rocha, Jeffery A Dodge, Cristian Coarfa, Venkatesh Krishnan, David R Rowley, Nancy L Weigel
JournalOncotarget (Oncotarget) Vol. 8 Issue 27 Pg. 44447-44464 (Jul 04 2017) ISSN: 1949-2553 [Electronic] United States
PMID28591703 (Publication Type: Journal Article)
Chemical References
  • Oncogene Protein p55(v-myc)
  • Receptors, Calcitriol
  • Transcriptional Regulator ERG
  • dihydroxy-vitamin D3
  • Vitamin D
  • Vitamin D3 24-Hydroxylase
  • Serine Endopeptidases
  • TMPRSS2 protein, human
Topics
  • Animals
  • Cell Line, Tumor
  • Cell Proliferation
  • Disease Models, Animal
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic
  • Heterografts
  • Humans
  • Male
  • Mice
  • Models, Biological
  • Oncogene Protein p55(v-myc) (metabolism)
  • Receptors, Calcitriol (agonists, metabolism)
  • Serine Endopeptidases (genetics)
  • Signal Transduction (drug effects)
  • Transcriptional Regulator ERG (genetics, metabolism)
  • Transcriptome
  • Tumor Burden
  • Vitamin D (analogs & derivatives, chemistry, pharmacology)
  • Vitamin D3 24-Hydroxylase (genetics, metabolism)
  • Xenograft Model Antitumor Assays

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