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Studies on the mechanism of cytotoxicity of 3-deazaguanosine in human cancer cells
The mechanism of toxicity of 3-deazaguanosine was studied in a number of human tumor cell lines by determination of the effects of various purine compounds on the growth of the cells in the presence of the drug and by studies of the effects of 3-deazaguanosine on the metabolism of radiolabeled precu...
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Published in: | Cancer chemotherapy and pharmacology 1985-05, Vol.15 (1), p.59-62 |
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container_title | Cancer chemotherapy and pharmacology |
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creator | PAGE, T JACOBSEN, S. J SMEJKAL, R. M SCHEELE, J NYHAN, W. L MANGUM, J. H ROBINS, R. K |
description | The mechanism of toxicity of 3-deazaguanosine was studied in a number of human tumor cell lines by determination of the effects of various purine compounds on the growth of the cells in the presence of the drug and by studies of the effects of 3-deazaguanosine on the metabolism of radiolabeled precursors in these cells. The drug was found to be toxic to all of the cell lines tested. The toxicity was reversible with removal of the drug. None of the purine bases tested could restore normal growth after 48 h exposure to 3-deazaguanosine; the bases were more effective in preventing cytotoxicity when added simultaneously with the drug. Metabolic studies indicated decreased synthesis of DNA, variable inhibition of de novo purine synthesis, and complete inhibition of the enzyme guanosine monophosphate reductase by 3-deazaguanosine. |
doi_str_mv | 10.1007/BF00257296 |
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Metabolic studies indicated decreased synthesis of DNA, variable inhibition of de novo purine synthesis, and complete inhibition of the enzyme guanosine monophosphate reductase by 3-deazaguanosine.</description><identifier>ISSN: 0344-5704</identifier><identifier>EISSN: 1432-0843</identifier><identifier>DOI: 10.1007/BF00257296</identifier><identifier>PMID: 4006050</identifier><identifier>CODEN: CCPHDZ</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Adenine - metabolism ; Antineoplastic agents ; Biological and medical sciences ; Cell Division - drug effects ; Cells, Cultured ; DNA - biosynthesis ; Formates - metabolism ; General aspects ; GMP Reductase ; Guanine - metabolism ; Guanosine - analogs & derivatives ; Guanosine - pharmacology ; Humans ; Medical sciences ; NADH, NADPH Oxidoreductases - metabolism ; Neoplasms - drug therapy ; Pharmacology. 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None of the purine bases tested could restore normal growth after 48 h exposure to 3-deazaguanosine; the bases were more effective in preventing cytotoxicity when added simultaneously with the drug. Metabolic studies indicated decreased synthesis of DNA, variable inhibition of de novo purine synthesis, and complete inhibition of the enzyme guanosine monophosphate reductase by 3-deazaguanosine.</description><subject>Adenine - metabolism</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Cell Division - drug effects</subject><subject>Cells, Cultured</subject><subject>DNA - biosynthesis</subject><subject>Formates - metabolism</subject><subject>General aspects</subject><subject>GMP Reductase</subject><subject>Guanine - metabolism</subject><subject>Guanosine - analogs & derivatives</subject><subject>Guanosine - pharmacology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>NADH, NADPH Oxidoreductases - metabolism</subject><subject>Neoplasms - drug therapy</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Purines - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PAGE, T</creatorcontrib><creatorcontrib>JACOBSEN, S. J</creatorcontrib><creatorcontrib>SMEJKAL, R. M</creatorcontrib><creatorcontrib>SCHEELE, J</creatorcontrib><creatorcontrib>NYHAN, W. L</creatorcontrib><creatorcontrib>MANGUM, J. H</creatorcontrib><creatorcontrib>ROBINS, R. K</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Cancer chemotherapy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PAGE, T</au><au>JACOBSEN, S. J</au><au>SMEJKAL, R. M</au><au>SCHEELE, J</au><au>NYHAN, W. L</au><au>MANGUM, J. H</au><au>ROBINS, R. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on the mechanism of cytotoxicity of 3-deazaguanosine in human cancer cells</atitle><jtitle>Cancer chemotherapy and pharmacology</jtitle><addtitle>Cancer Chemother Pharmacol</addtitle><date>1985-05</date><risdate>1985</risdate><volume>15</volume><issue>1</issue><spage>59</spage><epage>62</epage><pages>59-62</pages><issn>0344-5704</issn><eissn>1432-0843</eissn><coden>CCPHDZ</coden><abstract>The mechanism of toxicity of 3-deazaguanosine was studied in a number of human tumor cell lines by determination of the effects of various purine compounds on the growth of the cells in the presence of the drug and by studies of the effects of 3-deazaguanosine on the metabolism of radiolabeled precursors in these cells. The drug was found to be toxic to all of the cell lines tested. The toxicity was reversible with removal of the drug. None of the purine bases tested could restore normal growth after 48 h exposure to 3-deazaguanosine; the bases were more effective in preventing cytotoxicity when added simultaneously with the drug. Metabolic studies indicated decreased synthesis of DNA, variable inhibition of de novo purine synthesis, and complete inhibition of the enzyme guanosine monophosphate reductase by 3-deazaguanosine.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>4006050</pmid><doi>10.1007/BF00257296</doi><tpages>4</tpages></addata></record> |
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source | Springer LINK Archives |
subjects | Adenine - metabolism Antineoplastic agents Biological and medical sciences Cell Division - drug effects Cells, Cultured DNA - biosynthesis Formates - metabolism General aspects GMP Reductase Guanine - metabolism Guanosine - analogs & derivatives Guanosine - pharmacology Humans Medical sciences NADH, NADPH Oxidoreductases - metabolism Neoplasms - drug therapy Pharmacology. Drug treatments Purines - pharmacology |
title | Studies on the mechanism of cytotoxicity of 3-deazaguanosine in human cancer cells |
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