1α,25-Dihydroxyvitamin D3 is a preventive factor in the metastasis of lung cancer

被引:109
作者
Nakagawa, K
Kawaura, A
Kato, S
Takeda, E
Okano, T
机构
[1] Kobe Pharmaceut Univ, Dept Hyg Sci, Higashinada Ku, Kobe, Hyogo 6588558, Japan
[2] Univ Tokyo, Inst Mol & Cellular Biosci, Tokyo, Japan
[3] Univ Tokushima, Sch Med, Dept Clin Nutr, Tokushima, Japan
关键词
D O I
10.1093/carcin/bgh332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
1alpha,25-Dihydroxyvitamin D-3 [1alpha,25(OH)(2)D-3], the major regulator of calcium homeostasis, has potent antiproliferative and anti-invasive properties in vitro in cancer cells. Studies in vivo demonstrated that 1alpha,25(OH)(2)D-3 slows the progression of breast, prostate and other carcinomas. A key question is whether 1alpha,25(OH)(2)D-3 exerts its anticarcinogenic effects in vivo by a mechanism that is dependent on its capacity to limit the proliferation and invasiveness of cancer cells in vitro. It has not been clear whether the calcemic activity and regulation of the host defenses by 1alpha,25(OH)(2)D-3 contribute to the effect on cancer cells. In this study we have focused on the influence of 1alpha,25(OH)(2)D-3 on the metastasis of lung cancer, without involvement of the calcemic activity and other effects of 1alpha,25(OH)(2)D-3 in the host. We used metastatic Lewis lung carcinoma cells expressing green fluorescent protein (LLC-GFP cells) and examined metastatic activity in vitamin D receptor (VDR) null mutant (VDR-/-) mice and their wild-type counterparts (VDR+/+ mice). VDR-/- mice exhibit hypocalcemia and extremely high serum levels of 1alpha,25(OH)(2)D-3. We expected that serum 1alpha,25(OH)(2)D-3 would act in vivo to directly inhibit the metastatic growth of VDR-positive LLC-GFP cells in VDR-/- mice. The metastatic activities of LLC-GFP cells were remarkably reduced in VDR-/- mice compared with VDR+/+ mice. To test the hypothesis that serum 1alpha,25(OH)(2)D-3 is an intrinsic factor that inhibits metastatic growth of lung cancer cells, we corrected hypocalcemia and/or hypervitaminosis D in VDR-/- mice by dietary manipulation. The metastatic growth of LLC-GFP cells was remarkably reduced in response to serum levels of 1alpha,25(OH)(2)D-3, but not to serum calcium levels. Furthermore, we found that VDR+/+ mice fed the manipulated diets displayed an apparent inverse relationship between the physiological levels of serum 1alpha,25(OH)(2)D-3 (8-15 pg/ml) and tumorigenesis. Here we show that 1alpha,25(OH)(2)D-3 inhibits the metastatic growth of lung cancer cells in a defined animal model.
引用
收藏
页码:429 / 440
页数:12
相关论文
共 55 条
[1]   Migration of human monocytes in response to vascular endothelial growth factor (VEGF) is mediated via the VEGF receptor flt-1 [J].
Barleon, B ;
Sozzani, S ;
Zhou, D ;
Weich, HA ;
Mantovani, A ;
Marme, D .
BLOOD, 1996, 87 (08) :3336-3343
[2]   Calcium supplements for the prevention of colorectal adenomas [J].
Baron, JA ;
Beach, M ;
Mandel, JS ;
van Stolk, RU ;
Haile, RW ;
Sandler, RS ;
Rothstein, R ;
Summers, RW ;
Snover, DC ;
Beck, GJ ;
Bond, JH ;
Greenberg, ER .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (02) :101-107
[3]   STRUCTURE-FUNCTION-RELATIONSHIPS IN THE VITAMIN-D ENDOCRINE SYSTEM [J].
BOUILLON, R ;
OKAMURA, WH ;
NORMAN, AW .
ENDOCRINE REVIEWS, 1995, 16 (02) :200-257
[4]  
Boyapati SM, 2003, CANCER EPIDEM BIOMAR, V12, P631
[5]   Dairy products, calcium, phosphorous, vitamin D, and risk of prostate cancer (Sweden) [J].
Chan, JM ;
Giovannucci, E ;
Andersson, SO ;
Yuen, J ;
Adami, HO ;
Wolk, A .
CANCER CAUSES & CONTROL, 1998, 9 (06) :559-566
[6]  
Colton KW, 1999, CURR TOP STEROID RES, V2, P141
[7]   Regulation of extrarenal synthesis of 1,25-dihydroxyvitamin D3-relevance for colonic cancer prevention and therapy [J].
Cross, Heide S. ;
Kallay, Enikoe ;
Khorchide, Maya ;
Lechner, Daniel .
MOLECULAR ASPECTS OF MEDICINE, 2003, 24 (06) :459-465
[8]  
Cross HS, 2003, RECENT RES CANCER, V164, P413
[9]  
EISMAN JA, 1987, CANCER RES, V47, P21
[10]   The noncalcemic vitamin D analogs EB1089 and 22-oxacalcitriol suppress serum-induced parathyroid hormone-related peptide gene expression in a lung cancer cell line [J].
Falzon, M ;
Zong, J .
ENDOCRINOLOGY, 1998, 139 (03) :1046-1053