Tumor and Stem Cell Biology Interleukin-1a Mediates the Antiproliferative Effects of 1,25- Dihydroxyvitamin D3 in Prostate Progenitor/Stem Cells

نویسندگان

  • Sophia L. Maund
  • Wendy W. Barclay
  • Laura D. Hover
  • Linara S. Axanova
  • Guangchao Sui
  • Jason D. Hipp
  • James C. Fleet
  • Andrew Thorburn
  • Scott D. Cramer
چکیده

Vitamin D3 is a promising preventative and therapeutic agent for prostate cancer, but its implementation is hampered by a lack of understanding about its mechanism of action. Upon treatment with 1a,25-dihydroxyvitamin D3 [1,25(OH)2D3, vitamin D3], the metabolically active form of vitamin D3, adult prostate progenitor/ stem cells (PrP/SC) undergo cell-cycle arrest, senescence, and differentiation to an androgen receptor–positive luminal epithelial cell fate. Microarray analyses of controland vitamin D3–treated PrP/SCs revealed global gene expression signatures consistent with induction of differentiation. Interestingly, one of the most highly upregulated genes by vitamin D3 was the proinflammatory cytokine interleukin-1a (IL-1a). Systems biology analyses supported a central role for IL-1a in the vitamin D3 response in PrP/SCs. siRNA-mediated knockdown of IL-1a abrogated vitamin D3–induced growth suppression, establishing a requirement for IL-1a in the antiproliferative effects of vitamin D3 in PrP/SCs. These studies establish a system to study the molecular profile of PrP/SC differentiation, proliferation, and senescence, and they point to an important new role for IL-1a in vitamin D3 signaling in PrP/SCs. Cancer Res; 71(15); 5276–86. 2011 AACR.

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تاریخ انتشار 2011