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Chromosome band 11q23 translocation breakpoints are DNA topoisomerase II cleavage sites
Human leukemias with 11q23 translocations occur sporadically and after cancer treatment with DNA topoisomerase II-targeted drugs. To investigate this process, we examined DNA topoisomerase II cleavage in vitro in subclones of the normal 11q23 genomic homologue and a t(9;11) translocation breakpoint...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 1995-10, Vol.55 (19), p.4287-4292 |
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creator | FELIX, C. A LANGE, B. J HOSLER, M. R FERTALA, J BJORNSTI, M.-A |
description | Human leukemias with 11q23 translocations occur sporadically and after cancer treatment with DNA topoisomerase II-targeted drugs. To investigate this process, we examined DNA topoisomerase II cleavage in vitro in subclones of the normal 11q23 genomic homologue and a t(9;11) translocation breakpoint junction. Cleavage was assayed with limiting dilutions of enzyme in the presence or absence of epipodophyllotoxin and ATP. The strongest sites of cleavage coincided with the t(9;11) breakpoint site and two other translocation breakpoint sites within the normal homologue. These results support the involvement of DNA topoisomerase II in the translocation process at chromosome band 11q23. |
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A ; LANGE, B. J ; HOSLER, M. R ; FERTALA, J ; BJORNSTI, M.-A</creator><creatorcontrib>FELIX, C. A ; LANGE, B. J ; HOSLER, M. R ; FERTALA, J ; BJORNSTI, M.-A</creatorcontrib><description>Human leukemias with 11q23 translocations occur sporadically and after cancer treatment with DNA topoisomerase II-targeted drugs. To investigate this process, we examined DNA topoisomerase II cleavage in vitro in subclones of the normal 11q23 genomic homologue and a t(9;11) translocation breakpoint junction. Cleavage was assayed with limiting dilutions of enzyme in the presence or absence of epipodophyllotoxin and ATP. The strongest sites of cleavage coincided with the t(9;11) breakpoint site and two other translocation breakpoint sites within the normal homologue. These results support the involvement of DNA topoisomerase II in the translocation process at chromosome band 11q23.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 7671237</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Base Sequence ; Biological and medical sciences ; Chromosomes, Human, Pair 11 ; Chromosomes, Human, Pair 9 ; DNA Topoisomerases, Type II - physiology ; DNA-Binding Proteins - genetics ; Drug toxicity and drugs side effects treatment ; Histone-Lysine N-Methyltransferase ; Humans ; Introns ; Medical sciences ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Molecular Sequence Data ; Myeloid-Lymphoid Leukemia Protein ; Pharmacology. 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These results support the involvement of DNA topoisomerase II in the translocation process at chromosome band 11q23.</description><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Chromosomes, Human, Pair 11</subject><subject>Chromosomes, Human, Pair 9</subject><subject>DNA Topoisomerases, Type II - physiology</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Histone-Lysine N-Methyltransferase</subject><subject>Humans</subject><subject>Introns</subject><subject>Medical sciences</subject><subject>Miscellaneous (drug allergy, mutagens, teratogens...)</subject><subject>Molecular Sequence Data</subject><subject>Myeloid-Lymphoid Leukemia Protein</subject><subject>Pharmacology. 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R ; FERTALA, J ; BJORNSTI, M.-A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h269t-1a0d50c2b675b00a2ccce2a072d10af297a6959813af72ce349e74242fa86fa83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Chromosomes, Human, Pair 11</topic><topic>Chromosomes, Human, Pair 9</topic><topic>DNA Topoisomerases, Type II - physiology</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Histone-Lysine N-Methyltransferase</topic><topic>Humans</topic><topic>Introns</topic><topic>Medical sciences</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Molecular Sequence Data</topic><topic>Myeloid-Lymphoid Leukemia Protein</topic><topic>Pharmacology. Drug treatments</topic><topic>Proto-Oncogenes</topic><topic>Transcription Factors</topic><topic>Translocation, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FELIX, C. A</creatorcontrib><creatorcontrib>LANGE, B. J</creatorcontrib><creatorcontrib>HOSLER, M. R</creatorcontrib><creatorcontrib>FERTALA, J</creatorcontrib><creatorcontrib>BJORNSTI, M.-A</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>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FELIX, C. A</au><au>LANGE, B. J</au><au>HOSLER, M. R</au><au>FERTALA, J</au><au>BJORNSTI, M.-A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromosome band 11q23 translocation breakpoints are DNA topoisomerase II cleavage sites</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1995-10-01</date><risdate>1995</risdate><volume>55</volume><issue>19</issue><spage>4287</spage><epage>4292</epage><pages>4287-4292</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Human leukemias with 11q23 translocations occur sporadically and after cancer treatment with DNA topoisomerase II-targeted drugs. To investigate this process, we examined DNA topoisomerase II cleavage in vitro in subclones of the normal 11q23 genomic homologue and a t(9;11) translocation breakpoint junction. Cleavage was assayed with limiting dilutions of enzyme in the presence or absence of epipodophyllotoxin and ATP. The strongest sites of cleavage coincided with the t(9;11) breakpoint site and two other translocation breakpoint sites within the normal homologue. These results support the involvement of DNA topoisomerase II in the translocation process at chromosome band 11q23.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>7671237</pmid><tpages>6</tpages></addata></record> |
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subjects | Base Sequence Biological and medical sciences Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 9 DNA Topoisomerases, Type II - physiology DNA-Binding Proteins - genetics Drug toxicity and drugs side effects treatment Histone-Lysine N-Methyltransferase Humans Introns Medical sciences Miscellaneous (drug allergy, mutagens, teratogens...) Molecular Sequence Data Myeloid-Lymphoid Leukemia Protein Pharmacology. Drug treatments Proto-Oncogenes Transcription Factors Translocation, Genetic |
title | Chromosome band 11q23 translocation breakpoints are DNA topoisomerase II cleavage sites |
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