Vitamin D and prostate cancer: The role of membrane initiated signaling pathways in prostate cancer progression

被引:14
作者
Karlsson, Sandra [1 ]
Olausson, Josefin [1 ]
Lundh, Dan [1 ]
Sogard, Peter [1 ]
Mandal, Abut [1 ]
Holmstrom, Kjell-Ove [1 ]
Stahel, Anette [1 ]
Bengtsson, Jenny [1 ]
Larsson, Dennis [1 ]
机构
[1] Univ Skovde, Sch Life Sci, Syst Biol Res Ctr Biomed, S-54128 Skovde, Sweden
关键词
1,25(OH)(2)D-3; Prostate cancer; Membrane receptors; PDIA3; nVDR; Receptor modeling; 1,25D(3)-MEMBRANE-ASSOCIATED RAPID RESPONSE; D-RECEPTOR; 1-ALPHA; 25-DIHYDROXYVITAMIN D-3; CALCIUM-TRANSPORT; BINDING; PROTEIN; 1,25D(3)-MARRS; IDENTIFICATION; TRANSDUCTION; MATURATION;
D O I
10.1016/j.jsbmb.2010.03.083
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
1,25-Dihydroxyvitamin D-3 (1,25(OH)(2)D-3) has been demonstrated to mediate both genomic and non-genomic responses in prostate cancer (CaP) cells. Here, we give an overview of membrane initiated 1,25(OH)(2)D-3 signaling in prostate cancer cell progression. The presence of PDIA3 was investigated and homologous modeling of the putative PDIA3 receptor complex was conducted. Furthermore, the cellular distribution of nVDR was analyzed. We could show that both nVDR and PDIA3 are expressed in the prostate cancer cell lines investigated. The homologous modeling of PDIA3 showed that the receptor complex exists in a trimer formation, which suggests for allosteric activity. Our findings support previous reports and suggest that 1,25(OH)(2)D-3 is an important therapeutic agent in inhibiting prostate cancer progression. Furthermore, our data show that 1,25(OH)(2)D-3 regulate prostate cell biology via multiple pathways and targeting specific pathways for 1,25(OH)(2)D-3 might provide more effective therapies compared to the vitamin D therapies currently clinically tested. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:413 / 416
页数:4
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