| Literature DB >> 14342251 |
Abstract
1. A strain of Ehrlich ascites-tumour cells that showed little inhibition of growth in the presence of 6-mercaptopurine accumulated less than 5% as much 6-thioinosine 5'-phosphate in vivo, in the presence of 6-mercaptopurine, as did the sensitive strain from which it was derived. 2. Specific activities of the phosphoribosyltransferases that convert adenine, guanine, hypoxanthine and 6-mercaptopurine into AMP, GMP, IMP and 6-thioinosine 5'-phosphate were similar in extracts of the resistant and the sensitive cells. 3. As found previously with sensitive cells, 6-mercaptopurine is a competitive inhibitor of guanine phosphoribosyltransferase and hypoxanthine phosphoribosyltransferase from the resistant cells and does not inhibit the adenine phosphoribosyltransferase from these cells. Michaelis constants and inhibitor constants of the purine phosphoribosyltransferases from resistant cells did not differ significantly from those measured with the corresponding enzymes from sensitive cells. 4. Resistance to 6-mercaptopurine in this case is probably not due to qualitative or quantitative changes in these transferases.Entities:
Keywords: ADENINE; ADENINE NUCLEOTIDES; CARCINOMA, EHRLICH TUMOR; CHROMATOGRAPHY; ELECTROPHORESIS; ENZYME INHIBITORS; EXPERIMENTAL LAB STUDY; GLUCOSYLTRANSFERASES; GUANINE; GUANINE NUCLEOTIDES; HYPOXANTHINES; ION EXCHANGE RESINS; KINETICS; MERCAPTOPURINE; METABOLISM; NUCLEOTIDES; PHARMACOLOGY; XANTHINES
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Year: 1965 PMID: 14342251 PMCID: PMC1206407 DOI: 10.1042/bj0940071
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857