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Induction of erythroid differentiation and modulation of gene expression by tiazofurin in K-562 leukemia cells.

1988; National Academy of Sciences; Volume: 85; Issue: 17 Linguagem: Inglês

10.1073/pnas.85.17.6533

1091-6490

Edith Olàh, Yutaka Natsumeda, Tadashi Ikegami, Zsofia Kote, M. Horányi, Judit Szelényi, Edith Paulik, T. Kremmer, S. R. Hollan, J Sugár,

Acute Lymphoblastic Leukemia research

Tiazofurin (2-beta-D-ribofuranosyl-4-thiazole-carboxamide; NSC 286193), an antitumor carbon-linked nucleoside that inhibits IMP dehydrogenase (IMP:NAD+ oxidoreductase; EC 1.1.1.205) and depletes guanylate levels, can activate the erythroid differentiation program of K-562 human leukemia cells. Tiazofurin-mediated cell differentiation is a multistep process. The inducer initiates early (less than 6 hr) metabolic changes that precede commitment to differentiation; among these early changes are decreases in IMP dehydrogenase activity and in GTP concentration, as well as alterations in the expression of certain protooncogenes (c-Ki-ras). K-562 cells do express commitment-i.e., cells exhibit differentiation without tiazofurin. Guanosine was effective in preventing the action of tiazofurin, thus providing evidence that the guanine nucleotides are critically involved in tiazofurin-initiated differentiation. Activation of transcription of the erythroid-specific gene that encodes A gamma-globin is a late (48 hr) but striking effect of tiazofurin. Down-regulation of the c-ras gene appears to be part of the complex process associated with tiazofurin-induced erythroid differentiation and relates to the perturbations of GTP metabolism.