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二羟胆钙化醇对人慢性粒细胞白血病细胞中JunD的差异调节作用

Differential regulation of JunD by dihydroxycholecalciferol in human chronic myelogenous leukemia cells.

作者信息

Lasky S R, Iwata K, Rosmarin A G, Caprio D G, Maizel A L

机构信息

Roger Williams Medical Center, Section of Experimental Pathology, Providence, Rhode Island 02908, USA.

出版信息

J Biol Chem. 1995 Aug 25;270(34):19676-9. doi: 10.1074/jbc.270.34.19676.

Abstract

1,25-Dihydroxyvitamin D3 inhibits the proliferation of the chronic myelogenous leukemia cell line RWLeu-4 but not the resistant variant, JMRD3. Although these cells exhibit no detectable differences in the vitamin D receptor, alterations in the interaction of nuclear extracts with the osteocalcin-1,25-dihydroxyvitamin D3-response element are noted. It is shown herein that the 1,25-dihydroxyvitamin D3 receptor binds to the osteocalcin-1,25-dihydroxyvitamin D3-response element along with activator protein-1 (AP-1) complexes and that the DNA binding activities of members of the Jun and Fos proto-oncogene families, which make up the AP-1 transcription factor, are differentially regulated by 1,25-dihydroxyvitamin D3. It is shown that JunD DNA binding activity is enhanced by 1,25-dihydroxyvitamin D3 during cell cycle arrest in the sensitive cells but is decreased in the resistant cells. These results suggest that the level of JunD DNA binding activity may be a critical factor in the regulation of proliferation.

摘要

1,25 - 二羟基维生素D3可抑制慢性粒细胞白血病细胞系RWLeu - 4的增殖,但对耐药变体JMRD3无效。尽管这些细胞在维生素D受体上未表现出可检测到的差异,但核提取物与骨钙素 - 1,25 - 二羟基维生素D3反应元件的相互作用存在改变。本文表明,1,25 - 二羟基维生素D3受体与激活蛋白 - 1(AP - 1)复合物一起结合到骨钙素 - 1,25 - 二羟基维生素D3反应元件上,并且组成AP - 1转录因子的Jun和Fos原癌基因家族成员的DNA结合活性受到1,25 - 二羟基维生素D3的不同调节。结果显示,在敏感细胞的细胞周期停滞期间,1,25 - 二羟基维生素D3可增强JunD的DNA结合活性,但在耐药细胞中则降低。这些结果表明,JunD DNA结合活性水平可能是增殖调控的关键因素。

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