Problems with interphase fluorescence in situ hybridization in detecting BCR/ABL-positive cells in some patients using a novel technique with extra signals
Interphase fluorescence in situ hybridization (I-FISH) is frequently used to monitor the response to therapy in various hematological malignancies. We performed a comparison of I-FISH, metaphase FISH (C-FISH), conventional cytogenetics, spectral karyotyping (SKY) and PCR for the detection of the t(9...
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creator | Mohr, Brigitte Bornhäuser, Martin Platzbecker, Uwe Freiberg-Richter, Jens Naumann, Ralf Prange-Krex, Gabriele Mohm, Johannes Kroschinsky, Frank Ehninger, Gerhard Thiede, Christian |
description | Interphase fluorescence in situ hybridization (I-FISH) is frequently used to monitor the response to therapy in various hematological malignancies. We performed a comparison of I-FISH, metaphase FISH (C-FISH), conventional cytogenetics, spectral karyotyping (SKY) and PCR for the detection of the t(9;22) and the BCR/ABL rearrangement in 32 patients with chronic myelogenous leukemia (CML). FISH was done using a novel commercial probe set (VYSIS LSI BCR/ABL ES), which is designed to reduce the rate of false-positive results by marking the argininosuccinate synthetase (ASS) gene and thus providing an extra signal on chromosome 9. Our data indicate, that a substantial number of BCR/ABL-positive patients (
n=5 patients, 3 with Ph, 2 with masked Ph) present negative results using this probe set in I-FISH analyses, because they did not fulfill the scoring criteria. In fact, the ASS region, which usually remains on 9q in Ph+ CML, appears to be lost or translocated. Due to these results we recommend that the initial diagnosis as well as the follow-up of patients with Ph+ leukemias should not be based on a single technique but should integrate results of cytogenetics and molecular biology. |
doi_str_mv | 10.1016/S0165-4608(00)00371-X |
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n=5 patients, 3 with Ph, 2 with masked Ph) present negative results using this probe set in I-FISH analyses, because they did not fulfill the scoring criteria. In fact, the ASS region, which usually remains on 9q in Ph+ CML, appears to be lost or translocated. Due to these results we recommend that the initial diagnosis as well as the follow-up of patients with Ph+ leukemias should not be based on a single technique but should integrate results of cytogenetics and molecular biology.</description><identifier>ISSN: 0165-4608</identifier><identifier>EISSN: 1873-4456</identifier><identifier>DOI: 10.1016/S0165-4608(00)00371-X</identifier><identifier>PMID: 11425449</identifier><identifier>CODEN: CGCYDF</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Biological and medical sciences ; Bone Marrow - pathology ; Chromosome Banding ; Chromosomes, Human, Pair 22 ; Chromosomes, Human, Pair 9 ; Fusion Proteins, bcr-abl - analysis ; Fusion Proteins, bcr-abl - genetics ; Hematologic and hematopoietic diseases ; Humans ; In Situ Hybridization, Fluorescence - methods ; Interphase ; Karyotyping ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - blood ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Medical sciences ; Metaphase ; Reproducibility of Results ; Reverse Transcriptase Polymerase Chain Reaction ; Translocation, Genetic</subject><ispartof>Cancer genetics and cytogenetics, 2001-06, Vol.127 (2), p.111-117</ispartof><rights>2001 Elsevier Science Inc.</rights><rights>2001 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-98691e86f2cc26fed67f2daf44b3061b9f5af3c6cbb857853349c5043b6e60973</citedby><cites>FETCH-LOGICAL-c390t-98691e86f2cc26fed67f2daf44b3061b9f5af3c6cbb857853349c5043b6e60973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S016546080000371X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1031162$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11425449$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mohr, Brigitte</creatorcontrib><creatorcontrib>Bornhäuser, Martin</creatorcontrib><creatorcontrib>Platzbecker, Uwe</creatorcontrib><creatorcontrib>Freiberg-Richter, Jens</creatorcontrib><creatorcontrib>Naumann, Ralf</creatorcontrib><creatorcontrib>Prange-Krex, Gabriele</creatorcontrib><creatorcontrib>Mohm, Johannes</creatorcontrib><creatorcontrib>Kroschinsky, Frank</creatorcontrib><creatorcontrib>Ehninger, Gerhard</creatorcontrib><creatorcontrib>Thiede, Christian</creatorcontrib><title>Problems with interphase fluorescence in situ hybridization in detecting BCR/ABL-positive cells in some patients using a novel technique with extra signals</title><title>Cancer genetics and cytogenetics</title><addtitle>Cancer Genet Cytogenet</addtitle><description>Interphase fluorescence in situ hybridization (I-FISH) is frequently used to monitor the response to therapy in various hematological malignancies. We performed a comparison of I-FISH, metaphase FISH (C-FISH), conventional cytogenetics, spectral karyotyping (SKY) and PCR for the detection of the t(9;22) and the BCR/ABL rearrangement in 32 patients with chronic myelogenous leukemia (CML). FISH was done using a novel commercial probe set (VYSIS LSI BCR/ABL ES), which is designed to reduce the rate of false-positive results by marking the argininosuccinate synthetase (ASS) gene and thus providing an extra signal on chromosome 9. Our data indicate, that a substantial number of BCR/ABL-positive patients (
n=5 patients, 3 with Ph, 2 with masked Ph) present negative results using this probe set in I-FISH analyses, because they did not fulfill the scoring criteria. In fact, the ASS region, which usually remains on 9q in Ph+ CML, appears to be lost or translocated. Due to these results we recommend that the initial diagnosis as well as the follow-up of patients with Ph+ leukemias should not be based on a single technique but should integrate results of cytogenetics and molecular biology.</description><subject>Biological and medical sciences</subject><subject>Bone Marrow - pathology</subject><subject>Chromosome Banding</subject><subject>Chromosomes, Human, Pair 22</subject><subject>Chromosomes, Human, Pair 9</subject><subject>Fusion Proteins, bcr-abl - analysis</subject><subject>Fusion Proteins, bcr-abl - genetics</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence - methods</subject><subject>Interphase</subject><subject>Karyotyping</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - blood</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics</subject><subject>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Medical sciences</subject><subject>Metaphase</subject><subject>Reproducibility of Results</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Translocation, Genetic</subject><issn>0165-4608</issn><issn>1873-4456</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd1u1DAQhS0EotvCI4B8gRBchNqx4yRXqF3xJ60E4kfqneU4465RYqe2s7S8Ci-Ls7sC7riZkUbfmTmag9ATSl5RQsX5l1yqggvSvCDkJSGspsXVPbSiTc0KzitxH63-ICfoNMbvhJC6bMVDdEIpLyvO2xX69Sn4boAx4h82bbF1CcK0VRGwGWYfIGpwGvIcR5tmvL3rgu3tT5Wsd8u0hwQ6WXeNL9efzy8uN8XkM2l3gDUMQ9wr_Qh4yhJwKeI5LrTCzu9gwFm9dfZmhsN9uE1B5VPXTg3xEXpgcoPHx36Gvr1983X9vth8fPdhfbEpNGtJKtpGtBQaYUqtS2GgF7Upe2U47xgRtGtNpQzTQnddU9VNxRhvdUU46wQI0tbsDD0_7J2Cz05ikqONi3vlwM9R1qStGCdtBqsDqIOPMYCRU7CjCneSErmkIvepyOXlkhC5T0VeZd3T44G5G6H_qzrGkIFnR0BFrQYTlNM2_rOdUSrKjL0-YJC_sbMQZNR2yae3Iacge2__4-Q3BZisdA</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>Mohr, Brigitte</creator><creator>Bornhäuser, Martin</creator><creator>Platzbecker, Uwe</creator><creator>Freiberg-Richter, Jens</creator><creator>Naumann, Ralf</creator><creator>Prange-Krex, Gabriele</creator><creator>Mohm, Johannes</creator><creator>Kroschinsky, Frank</creator><creator>Ehninger, Gerhard</creator><creator>Thiede, Christian</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20010601</creationdate><title>Problems with interphase fluorescence in situ hybridization in detecting BCR/ABL-positive cells in some patients using a novel technique with extra signals</title><author>Mohr, Brigitte ; Bornhäuser, Martin ; Platzbecker, Uwe ; Freiberg-Richter, Jens ; Naumann, Ralf ; Prange-Krex, Gabriele ; Mohm, Johannes ; Kroschinsky, Frank ; Ehninger, Gerhard ; Thiede, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-98691e86f2cc26fed67f2daf44b3061b9f5af3c6cbb857853349c5043b6e60973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Biological and medical sciences</topic><topic>Bone Marrow - pathology</topic><topic>Chromosome Banding</topic><topic>Chromosomes, Human, Pair 22</topic><topic>Chromosomes, Human, Pair 9</topic><topic>Fusion Proteins, bcr-abl - analysis</topic><topic>Fusion Proteins, bcr-abl - genetics</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence - methods</topic><topic>Interphase</topic><topic>Karyotyping</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - blood</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics</topic><topic>Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. 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We performed a comparison of I-FISH, metaphase FISH (C-FISH), conventional cytogenetics, spectral karyotyping (SKY) and PCR for the detection of the t(9;22) and the BCR/ABL rearrangement in 32 patients with chronic myelogenous leukemia (CML). FISH was done using a novel commercial probe set (VYSIS LSI BCR/ABL ES), which is designed to reduce the rate of false-positive results by marking the argininosuccinate synthetase (ASS) gene and thus providing an extra signal on chromosome 9. Our data indicate, that a substantial number of BCR/ABL-positive patients (
n=5 patients, 3 with Ph, 2 with masked Ph) present negative results using this probe set in I-FISH analyses, because they did not fulfill the scoring criteria. In fact, the ASS region, which usually remains on 9q in Ph+ CML, appears to be lost or translocated. Due to these results we recommend that the initial diagnosis as well as the follow-up of patients with Ph+ leukemias should not be based on a single technique but should integrate results of cytogenetics and molecular biology.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>11425449</pmid><doi>10.1016/S0165-4608(00)00371-X</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Bone Marrow - pathology Chromosome Banding Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 9 Fusion Proteins, bcr-abl - analysis Fusion Proteins, bcr-abl - genetics Hematologic and hematopoietic diseases Humans In Situ Hybridization, Fluorescence - methods Interphase Karyotyping Leukemia, Myelogenous, Chronic, BCR-ABL Positive - blood Leukemia, Myelogenous, Chronic, BCR-ABL Positive - genetics Leukemia, Myelogenous, Chronic, BCR-ABL Positive - pathology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Medical sciences Metaphase Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction Translocation, Genetic |
title | Problems with interphase fluorescence in situ hybridization in detecting BCR/ABL-positive cells in some patients using a novel technique with extra signals |
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