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Cytidine triphosphate synthetase activity in lymphoproliferative disorders
Cytidine triphosphate synthetase (CTP synthetase) activity was measured in extracts from normal and malignant lymphoid cells. A range of enzyme activities was found in the majority of the lymphoproliferative disorders examined, with acute lymphocytic leukemia, nodular poorly differentiated lymphocyt...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 1983-03, Vol.43 (3), p.1432-1435 |
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container_title | Cancer research (Chicago, Ill.) |
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creator | Ellims, P H Gan, T E Medley, G |
description | Cytidine triphosphate synthetase (CTP synthetase) activity was measured in extracts from normal and malignant lymphoid cells. A range of enzyme activities was found in the majority of the lymphoproliferative disorders examined, with acute lymphocytic leukemia, nodular poorly differentiated lymphocytic lymphoma, and diffuse histiocytic (large cell) lymphoma (DHL) types exhibiting the widest ranges. It is suggested that CTP synthetase activity is a biochemical marker of the clinical aggressiveness of malignant lymphoma. There was not a close correlation (r super(2) = 0.52) between CTP synthetase and thymidine kinase activities, indicating that other biological factors in addition to cell proliferative rate influence the intracellular CTP synthetase level. Furthermore, in view of the heterogeneity of CTP synthetase activity in leukemia and lymphoma, it is likely that the preexisting enzyme level will be an important determinant of the efficacy of the investigational antileukemic agent 3-deazauridine, which is thought to act by inhibiting CTP synthetase. |
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A range of enzyme activities was found in the majority of the lymphoproliferative disorders examined, with acute lymphocytic leukemia, nodular poorly differentiated lymphocytic lymphoma, and diffuse histiocytic (large cell) lymphoma (DHL) types exhibiting the widest ranges. It is suggested that CTP synthetase activity is a biochemical marker of the clinical aggressiveness of malignant lymphoma. There was not a close correlation (r super(2) = 0.52) between CTP synthetase and thymidine kinase activities, indicating that other biological factors in addition to cell proliferative rate influence the intracellular CTP synthetase level. Furthermore, in view of the heterogeneity of CTP synthetase activity in leukemia and lymphoma, it is likely that the preexisting enzyme level will be an important determinant of the efficacy of the investigational antileukemic agent 3-deazauridine, which is thought to act by inhibiting CTP synthetase.</description><identifier>ISSN: 0008-5472</identifier><identifier>PMID: 6572096</identifier><language>eng</language><publisher>United States</publisher><subject>Carbon-Nitrogen Ligases ; Hodgkin Disease - enzymology ; Humans ; Leukemia, Lymphoid - enzymology ; Ligases - metabolism ; Lymph Nodes - enzymology ; Lymphocytes - enzymology ; Lymphoma - enzymology ; Lymphoproliferative Disorders - enzymology ; Thymidine Kinase - metabolism</subject><ispartof>Cancer research (Chicago, Ill.), 1983-03, Vol.43 (3), p.1432-1435</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6572096$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ellims, P H</creatorcontrib><creatorcontrib>Gan, T E</creatorcontrib><creatorcontrib>Medley, G</creatorcontrib><title>Cytidine triphosphate synthetase activity in lymphoproliferative disorders</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Cytidine triphosphate synthetase (CTP synthetase) activity was measured in extracts from normal and malignant lymphoid cells. A range of enzyme activities was found in the majority of the lymphoproliferative disorders examined, with acute lymphocytic leukemia, nodular poorly differentiated lymphocytic lymphoma, and diffuse histiocytic (large cell) lymphoma (DHL) types exhibiting the widest ranges. It is suggested that CTP synthetase activity is a biochemical marker of the clinical aggressiveness of malignant lymphoma. There was not a close correlation (r super(2) = 0.52) between CTP synthetase and thymidine kinase activities, indicating that other biological factors in addition to cell proliferative rate influence the intracellular CTP synthetase level. Furthermore, in view of the heterogeneity of CTP synthetase activity in leukemia and lymphoma, it is likely that the preexisting enzyme level will be an important determinant of the efficacy of the investigational antileukemic agent 3-deazauridine, which is thought to act by inhibiting CTP synthetase.</description><subject>Carbon-Nitrogen Ligases</subject><subject>Hodgkin Disease - enzymology</subject><subject>Humans</subject><subject>Leukemia, Lymphoid - enzymology</subject><subject>Ligases - metabolism</subject><subject>Lymph Nodes - enzymology</subject><subject>Lymphocytes - enzymology</subject><subject>Lymphoma - enzymology</subject><subject>Lymphoproliferative Disorders - enzymology</subject><subject>Thymidine Kinase - metabolism</subject><issn>0008-5472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLxTAUhLNQrterP0Hoyl3hJGnSdCnFJxfc6LqkyQmN9GWSCv33Fuze1TDMxzDMBTkCgMpFUbIrch3j12YFBXEgBylKBpU8krd6Td76EbMU_NxNce50wiyuY-ow6YiZNsn_-LRmfsz6ddiYOUy9dxj0FmBmfZyCxRBvyKXTfcTbXU_k8-nxo37Jz-_Pr_XDOe9YCSm3ilFOhQPGigKFQ9YqCw4MkxWnVJRUVqCgBOmwBVOgZYCVcsZQ5AYFP5H7v95tx_eCMTWDjwb7Xo84LbFRwEsmOfwLUi5kIZTcwLsdXNoBbTMHP-iwNvtL_BcHs2N0</recordid><startdate>19830301</startdate><enddate>19830301</enddate><creator>Ellims, P H</creator><creator>Gan, T E</creator><creator>Medley, G</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19830301</creationdate><title>Cytidine triphosphate synthetase activity in lymphoproliferative disorders</title><author>Ellims, P H ; Gan, T E ; Medley, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h270t-d821315f02244e5fe2b8d0f0c26931157169080706feb0c4ed20e98fcc1e3ce53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Carbon-Nitrogen Ligases</topic><topic>Hodgkin Disease - enzymology</topic><topic>Humans</topic><topic>Leukemia, Lymphoid - enzymology</topic><topic>Ligases - metabolism</topic><topic>Lymph Nodes - enzymology</topic><topic>Lymphocytes - enzymology</topic><topic>Lymphoma - enzymology</topic><topic>Lymphoproliferative Disorders - enzymology</topic><topic>Thymidine Kinase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ellims, P H</creatorcontrib><creatorcontrib>Gan, T E</creatorcontrib><creatorcontrib>Medley, G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ellims, P H</au><au>Gan, T E</au><au>Medley, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytidine triphosphate synthetase activity in lymphoproliferative disorders</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1983-03-01</date><risdate>1983</risdate><volume>43</volume><issue>3</issue><spage>1432</spage><epage>1435</epage><pages>1432-1435</pages><issn>0008-5472</issn><abstract>Cytidine triphosphate synthetase (CTP synthetase) activity was measured in extracts from normal and malignant lymphoid cells. A range of enzyme activities was found in the majority of the lymphoproliferative disorders examined, with acute lymphocytic leukemia, nodular poorly differentiated lymphocytic lymphoma, and diffuse histiocytic (large cell) lymphoma (DHL) types exhibiting the widest ranges. It is suggested that CTP synthetase activity is a biochemical marker of the clinical aggressiveness of malignant lymphoma. There was not a close correlation (r super(2) = 0.52) between CTP synthetase and thymidine kinase activities, indicating that other biological factors in addition to cell proliferative rate influence the intracellular CTP synthetase level. Furthermore, in view of the heterogeneity of CTP synthetase activity in leukemia and lymphoma, it is likely that the preexisting enzyme level will be an important determinant of the efficacy of the investigational antileukemic agent 3-deazauridine, which is thought to act by inhibiting CTP synthetase.</abstract><cop>United States</cop><pmid>6572096</pmid><tpages>4</tpages></addata></record> |
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subjects | Carbon-Nitrogen Ligases Hodgkin Disease - enzymology Humans Leukemia, Lymphoid - enzymology Ligases - metabolism Lymph Nodes - enzymology Lymphocytes - enzymology Lymphoma - enzymology Lymphoproliferative Disorders - enzymology Thymidine Kinase - metabolism |
title | Cytidine triphosphate synthetase activity in lymphoproliferative disorders |
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