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Vitamin D favorably alters the cancer promoting prostaglandin cascade.

AbstractBACKGROUND:
Preclinical studies suggest that 1,25-dihydroxyvitamin D [1,25(OH)2D] and celecoxib inhibit prostaglandins (PGs) associated with cancer through different mechanisms. We determined if there was synergy in their use.
PATIENTS AND METHODS:
A total of 36 healthy women received daily for one month/menstrual cycle: placebo, 400 international units (IU) vitamin D-3, 2,000 IU vitamin D-3, or 2,000 IU vitamin D-3 plus 400 mg celecoxib. Serum and nipple aspirate fluid (NAF) were analyzed for PGE2 and transforming growth factor (TGF)β1 and -2; serum for 25(OH)D (total, -D-2, -D-3), plasma for celecoxib; and mammary duct RNA for cyclooxygenase (COX)2.
RESULTS:
25(OH)D-3 increased (p<0.01) only in the groups receiving 2,000 IU vitamin D-3. PGE2 decreased in the breast (p=0.01) only after receiving 2,000 IU vitamin D-3; 2,000 IU vitamin D-3 alone was more effective in decreasing PGE2 than 2,000 IU vitamin D-3 plus celecoxib (p=0.018). COX2 expression decreased only in the breasts of women taking 2,000 IU vitamin D-3. Change in circulating 25(OH)D-3 correlated with change in TGFβ2 in the breast.
CONCLUSION:
Vitamin D-3 reduces the PG cascade and increases TGFβ2 in a dose-dependent fashion. Adding celecoxib did not provide synergy.
AuthorsWenyi Qin, Claris Smith, Mark Jensen, Michael F Holick, Edward R Sauter
JournalAnticancer research (Anticancer Res) Vol. 33 Issue 9 Pg. 3861-6 (Sep 2013) ISSN: 1791-7530 [Electronic] Greece
PMID24023320 (Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Placebos
  • Prostaglandin Antagonists
  • Pyrazoles
  • Sulfonamides
  • Transforming Growth Factor beta
  • Vitamin D
  • Cholecalciferol
  • RNA
  • 25-hydroxyvitamin D
  • Cyclooxygenase 2
  • Celecoxib
  • Dinoprostone
Topics
  • Adult
  • Celecoxib
  • Cholecalciferol (pharmacology)
  • Cyclooxygenase 2 (genetics)
  • Dinoprostone (blood, metabolism)
  • Double-Blind Method
  • Female
  • Humans
  • Middle Aged
  • Neoplasms (metabolism)
  • Placebos
  • Prostaglandin Antagonists (pharmacology)
  • Pyrazoles (pharmacology)
  • RNA (blood)
  • Reference Values
  • Sulfonamides (pharmacology)
  • Transforming Growth Factor beta (blood)
  • Vitamin D (analogs & derivatives, blood)

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