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  • Title: Induction of differentiation of human myeloid leukemia HL-60 cells by novel pyrimidine nucleoside analogs.
    Author: Makishima M, Honma Y, Hozumi M, Sampi K, Hattori M, Ishikawa I, Ogura H, Kawahara N, Kanaiwa T, Motoyoshi K.
    Journal: Biochim Biophys Acta; 1991 Aug 13; 1094(1):1-7. PubMed ID: 1883847.
    Abstract:
    New pyrimidine nucleoside analogs (18 compounds) were synthesized and their growth-inhibiting and differentiation-inducing activities on human myeloid leukemia HL-60 cells were examined. Some of the analogs were found to induce nitroblue tetrazolium (NBT) reducing activity in the HL-60 cells. The inducing activities of these compounds were compared at their concentrations for 50% inhibition of cell growth. TI-79 (3-benzyl-5-methyl-3-(beta-D-ribofuranosyl)pyrido[2,3-d]pyrimidine- 2,4(1H,3H)-dione) was a very effective inducer of NBT-reduction and of differentiation of the cells into mature granulocytes. The induction of NBT-reducing activity by TI-79 was inhibited by high concentrations of the natural nucleoside, adenosine. Other differentiation inducers, such as retinoic acid, 1 alpha,25-dihydroxyvitamin D-3 and staurosporin markedly enhanced the induction of differentiation of HL-60 cells by TI-79. Nucleoside analogs such as TI-79 should be useful for differentiation therapy of some types of myelogenous leukemia.
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