Mara Banks1, Michael F Holick2. 1. Vitamin D, Skin and Bone Research Laboratory, Division of Endocrinology, Diabetes and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, MA, U.S.A. 2. Vitamin D, Skin and Bone Research Laboratory, Division of Endocrinology, Diabetes and Nutrition, Department of Medicine, Boston University School of Medicine, Boston, MA, U.S.A. mfholick@bu.edu.
Abstract
BACKGROUND/AIM: 1α,25(OH)2D has been shown to induce cell-cycle regulation, apoptosis and differentiation in prostate cancer cells. Previous studies have demonstrated that prostate and some prostate cancer cells have the ability to convert 25(OH)D3 to 1α,25(OH)2D3. The aim of the present study was to elucidate the role of 1α,25(OH)2D3 production by 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1) on prostate cancer cell growth. MATERIALS AND METHODS: LNCaP cells were stably transfected with CYP27B. RESULTS: Stably-transfected 1α-OHase LNCaP cells converted 25(OH)D3 to 1α,25(OH)2D3 unlike untransfected LNCaP cells. There was a dose-dependent decrease in (3)H-thymidine incorporation in 1α,25(OH)2D3-treated LNCaP cells, not seen with 25(OH)D3 treatment, and in stably transfected 1α-OHase LNCaP cells treated with 25(OH)D3. 1α,25(OH)2D3-treated LNCaP cells and 25(OH)D3-treated stably-transfected 1α-OHase LNCaP cells demonstrated an increased G1 phase accumulation and apoptosis, while 25(OH)D3 treatment had no effect in LNCaP cells. CONCLUSION: The present study supports the hypothesis that local production of 1α,25(OH)2D is important in inhibiting prostate cancer development and growth. Copyright
BACKGROUND/AIM: 1α,25(OH)2D has been shown to induce cell-cycle regulation, apoptosis and differentiation in prostate cancer cells. Previous studies have demonstrated that prostate and some prostate cancer cells have the ability to convert 25(OH)D3 to 1α,25(OH)2D3. The aim of the present study was to elucidate the role of 1α,25(OH)2D3 production by 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1) on prostate cancer cell growth. MATERIALS AND METHODS: LNCaP cells were stably transfected with CYP27B. RESULTS: Stably-transfected 1α-OHase LNCaP cells converted 25(OH)D3 to 1α,25(OH)2D3 unlike untransfected LNCaP cells. There was a dose-dependent decrease in (3)H-thymidine incorporation in 1α,25(OH)2D3-treated LNCaP cells, not seen with 25(OH)D3 treatment, and in stably transfected 1α-OHase LNCaP cells treated with 25(OH)D3. 1α,25(OH)2D3-treated LNCaP cells and 25(OH)D3-treated stably-transfected 1α-OHase LNCaP cells demonstrated an increased G1 phase accumulation and apoptosis, while 25(OH)D3 treatment had no effect in LNCaP cells. CONCLUSION: The present study supports the hypothesis that local production of 1α,25(OH)2D is important in inhibiting prostate cancer development and growth. Copyright
Authors: Visalini Nair-Shalliker; Albert Bang; Sam Egger; Mark Clements; Robert A Gardiner; Anne Kricker; Markus J Seibel; Suzanne K Chambers; Michael G Kimlin; Bruce K Armstrong; David P Smith Journal: Sci Rep Date: 2020-05-08 Impact factor: 4.379
Authors: Tara McCray; Julian V Pacheco; Candice C Loitz; Jason Garcia; Bethany Baumann; Michael J Schlicht; Klara Valyi-Nagy; Michael R Abern; Larisa Nonn Journal: iScience Date: 2021-01-05