1,25-Dihydroxyvitamin D3 induced cell cycle arrest in the human primary liver cancer cell line HepG2

被引:18
作者
Caputo, A [1 ]
Pourgholami, MH [1 ]
Akhter, J [1 ]
Morris, DL [1 ]
机构
[1] Univ New S Wales, St George Hosp, Dept Surg, Sydney, NSW 2217, Australia
关键词
hepatocellular carcinoma; vitamin D3 receptor; cell cycle; VITAMIN-D-RECEPTOR; HEPATOCELLULAR-CARCINOMA; IN-VITRO; 1-ALPHA; 25-DIHYDROXYVITAMIN D-3; GROWTH-INHIBITION; ANALOG EB-1089; APOPTOSIS; MCF-7; PROLIFERATION; SUPPRESSION;
D O I
10.1016/S1386-6346(02)00328-5
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The inhibitory effect of 1,25-dihydroxyvitamin D-3 (1,25-(OH)(2)D-3) on the proliferation of a number of human and rat liver cancer cell lines has recently been reported. In this study we have demonstrated that these cell lines express functional receptors able to specifically bind [H-3]1,25-(OH)(2)D-3. The highest level of functional receptor were found in the human liver cancer cell line HepG2 which had previously been shown to be the most sensitive in 1,25-(OH)2D3 growth inhibition assays. The identity of the binding protein with the Vitamin D3 receptor was confirmed by PCR analysis of HepG2 cell mRNA. Additionally, the inhibitory effect of 1,25-(OH)(2)D-3 on growth of the human liver cancer cell line HepG2 resulted from arrest in the G0/G1 phase of the cell cycle. Increases in the fraction of cells in G0/G1 were dependent upon the concentration of 1,25-(OH)(2)D-3 and were accompanied by complementary decreases in the number of cells in S phase. There was no change in the number of cells in G2+M at any concentration of the hormone. Clonal growth of HepG2 cells in response to 1,25-(OH)(2)D-3 was also dose dependent over three orders of magnitude, thus indicating heterogeneity in cell cycle arrest by this hormone. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
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页码:34 / 39
页数:6
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