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Induction of Erythroid Differentiation in Leukemic K562 Cells by an S-Adenosylhomocysteine Hydrolase Inhibitor, Aristeromycin
Ist Teil von
Biochemical and biophysical research communications, 1995-02, Vol.207 (1), p.69-74
Ort / Verlag
Elsevier Inc
Erscheinungsjahr
1995
Link zum Volltext
Quelle
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
Beschreibungen/Notizen
We have isolated an unusual nucleoside, aristeromycin, from the culture filtrate of
Actinomycetes as a compound that induces normal morphology in v-abl
ts-NIH3T3 cells. Aristeromycin also induced erythroid differentiation in abl-expressing human chronic myelogenous leukaemia K562 cells. It did not affect the amount of Abl or the Abl-associated tyrosine kinase activity in either v-abl
ts-NIH3T3 or K562 cells. As a potent inhibitor of S-adenosylhomocysteine hydrolase, aristeromycin inhibited methylation of phosphatidylethanolamine to form phosphatidylcholine in K562 cells. Among aristeromycin analogues, the activity to inhibit S-adenosylhomocysteine hydrolase was paralleled with the induction of erythroid differentiation. Thus, aristeromycin inhibits abl functions indirectly, possibly by inhibiting biological methylations.