Regulation of proliferation of prostate epithelial cells by 1,25-dihydroxyvitamin D3 is accompanied by an increase in insulin-like growth factor binding protein-3

被引:35
|
作者
Sprenger, CC
Peterson, A
Lance, AR
Ware, JL
Drivdahl, RH
Plymate, SR
机构
[1] Amer Lake VAMC, GRECC 182B, VAPSHCS, Tacoma, WA 98493 USA
[2] Madigan Army Med Ctr, Dept Urol, Tacoma, WA 98431 USA
[3] VCU, MCV, Dept Pathol, Richmond, VA USA
[4] Univ Washington, Dept Med, Seattle, WA USA
关键词
D O I
10.1677/joe.0.1700609
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The biologically active form of vitamin D, 1,25-dihydroxyvitamin D-3 (1,25-(OH)A) has been shown to regulate the proliferation of human prostate epithelial cell lines. Since the insulin-like growth factor (IGF) system is involved in the transformation process of epithelial cells, the following study was undertaken to determine if the IGF system, in particular IGF binding protein-3 (IGFBP-3), is altered by 1,25-(OH)(2)D-3 in normal prostate epithelial cells as part of a mechanism for inhibition of transformation. Two cell systems were used in this study: (1) primary Cultures of benign human prostate epithelial cells (PECs) and (2) an SV40-T immortalized prostate epithelial cell Line (P153) that is non-tumorigenic. 1,25-(OH)(2)D-3 was added to parallel sets of PECs and P153 cells in addition to the presence or absence of IGF-I or des(1-3)IGF-I. Treatment with 1,25-(OH)2D3 resulted in significant growth inhibition of both PECs and P153 cells. Furthermore, 1,25-(OH)2D3 inhibited IGF-induced proliferation, but this was partially reversed by high concentrations of IGF-I. Western ligand blots of condition media demonstrated a significant increase in IGFBP-3; likewise Northern blots demonstrated an increase in mRNA for IGFBP-3. Proliferation assays using an antibody designed to block the IGF-independent effects of IGFBP-3 failed to reverse the inhibitory effect of 1,25-(OH)(2)D-3. Thus, IGFBP-3 acts in an IGF-dependent manner to inhibit cell growth of benign prostate epithelial cells.
引用
收藏
页码:609 / 618
页数:10
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