Department of Pathology and Laboratory Medicine, UMDNJ-New Jersey, Medical School, Newark, NJ 07103, USA.
J Steroid Biochem Mol Biol. 2010 Jul;121(1-2):395-8. doi: 10.1016/j.jsbmb.2010.03.016. Epub 2010 Mar 19.
The role of MAP kinase pathways in 1,25-dihydroxyvitamin D3 (1,25D)-induced differentiation of myeloid leukemia cells is well established, but the mechanisms by which 1,25D activates these pathways are not entirely clear. Following the finding that kinase suppressors of ras (KSR) 1 and 2 are directly regulated by 1,25D and participate in the monocytic differentiation process, we investigated if the COT1 oncogene (Tpl2 in the rat), known to interact with human KSR2 (hKSR2), is also involved in 1,25D-induced differentiation in leukemia cells. Here we report that the exposure of HL60 and U937 myeloid leukemia cells to 1,25D increases COT1 expression in a concentration-dependent manner. However, COT1 appears to have a differentiation-limiting role in these cells, as an exposure of HL60 and U937 cells to a pharmacological inhibitor of COT1 kinase activity, 4-(3-chloro-4-fluorophenylamino)-6-(pyridin-3-yl-methylamino-3-cyano-[1-7]-naphthyridine, results in increased 1,25D-induced differentiation. These findings provide an additional insight into the 1,25D-regulation of MAPK pathways that contribute to monocytic differentiation process of myeloid leukemia cells.
MAP 激酶途径在 1,25-二羟维生素 D3(1,25D)诱导髓样白血病细胞分化中的作用已得到充分证实,但 1,25D 激活这些途径的机制尚不完全清楚。在发现激酶抑制剂 Ras(KSR)1 和 2 被 1,25D 直接调节并参与单核细胞分化过程后,我们研究了 COT1 癌基因(大鼠中的 Tpl2)是否也参与白血病细胞中 1,25D 诱导的分化。在这里,我们报告说,HL60 和 U937 髓样白血病细胞暴露于 1,25D 会以浓度依赖性方式增加 COT1 的表达。然而,COT1 在这些细胞中似乎具有分化限制作用,因为 HL60 和 U937 细胞暴露于 COT1 激酶活性的药理学抑制剂 4-(3-氯-4-氟苯基氨基)-6-(吡啶-3-基甲基氨基-3-氰基-[1-7]-萘啶)会导致 1,25D 诱导的分化增加。这些发现为 1,25D 调节 MAPK 途径提供了更多的见解,这些途径有助于髓样白血病细胞的单核细胞分化过程。