TY - JOUR
T1 - The role of vitamine D3 in the proliferation of a human colon cancer cell line in vitro
AU - Lointier, P.
AU - Wargovich, M. J.
AU - Saez, S.
AU - Levin, B.
AU - Wildrick, D. M.
AU - Boman, B. M.
PY - 1987/1/1
Y1 - 1987/1/1
N2 - LoVo, a cultured colon cancer cell line, is shown to posses a receptor for 1,25-dihydroxy vitamin D3 (1α,25(OH)2D3) with a low capacity (28 fmol/mg protein) and high affinity (Kd: 1.9 x 10(-21O)M). When these cells were grown in monolayer culture in a chemically defined serum-free medium, a significant inhibition of proliferation was seen in the presence of 10 nM to 1μM of 1α,25(OH)2D3 (p<0.005). Furthermore, 1α,25(OH)2D3 delayed early attachment of cells. After 8 days of treatment, aggregated cuboidal cells showed a marked change to an apparently spindle like morphology. The 1α,25(OH)2D3 growth-inhibitory effect was modulated by verapamil (1 μM), a calcium channel blocker, hydrocortisone (1 μM) and moxestrol (1 mM), an estrogen analogue, and 2% charcoal-treated fetal bovine serum. This study represents the first demonstration of 1α,25(OH)2D3 modulation of growth of human colon cells.
AB - LoVo, a cultured colon cancer cell line, is shown to posses a receptor for 1,25-dihydroxy vitamin D3 (1α,25(OH)2D3) with a low capacity (28 fmol/mg protein) and high affinity (Kd: 1.9 x 10(-21O)M). When these cells were grown in monolayer culture in a chemically defined serum-free medium, a significant inhibition of proliferation was seen in the presence of 10 nM to 1μM of 1α,25(OH)2D3 (p<0.005). Furthermore, 1α,25(OH)2D3 delayed early attachment of cells. After 8 days of treatment, aggregated cuboidal cells showed a marked change to an apparently spindle like morphology. The 1α,25(OH)2D3 growth-inhibitory effect was modulated by verapamil (1 μM), a calcium channel blocker, hydrocortisone (1 μM) and moxestrol (1 mM), an estrogen analogue, and 2% charcoal-treated fetal bovine serum. This study represents the first demonstration of 1α,25(OH)2D3 modulation of growth of human colon cells.
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M3 - Article
C2 - 2823686
AN - SCOPUS:0023369048
SN - 0250-7005
VL - 7
SP - 817
EP - 522
JO - Anticancer Research
JF - Anticancer Research
IS - 4 B
ER -