PMID- 21461967 OWN - NLM STAT- MEDLINE DCOM- 20120918 LR - 20211020 IS - 1559-131X (Electronic) IS - 1357-0560 (Linking) VI - 29 IP - 2 DP - 2012 Jun TI - Molecular cytogenetic study of derivative chromosome 9 deletion in chronic myeloid leukemia patients. PG - 1151-60 LID - 10.1007/s12032-011-9918-8 [doi] AB - The aims of this study are to investigate the frequency of derivative chromosome 9 (der (9)) deletion in Tunisian patients with chronic myeloid leukemia (CML) and to assess the correlation between this deletion and the cytogenetic response for patients treated with hydroxyurea (HU) or imatinib (IM). Karyotype analysis of 336 patients with CML was performed with R-banding technique. Fluorescence in situ hybridization (FISH) was carried using home-brew probes 17L7 and 248J22 for detecting, respectively, adjacent 5'ABL and 3'BCR deletions on der(9). Cytogenetic study demonstrated typical t(9;22)(q34;q11) translocation in 89.6% and variant translocation in 10.4% of patients. Interphase FISH studies showed deletion of der(9) in 59 (17.6%) of the 336 patients, 23 (39%) of them had variant rearrangements. There are 19 patients with solely 5'ABL deletion and 40 with concomitant 5'ABL and 3'BCR deletions. Cytogenetic response was evaluated during 18 months with HU or IM therapy. Our results demonstrate that (a) 3'BCR deletion is associated with 5'ABL deletion in all patients with der(9) deletions, (b) the 5'ABL and 3'BCR deletions arise simultaneously with t(9;22), (c) deletions on der(9) chromosome were frequently encountered in older patients and in patients presenting variant rearrangements, (d) both 5'ABL and 3'BCR deletions were associated with cytogenetic response failure in patients treated with HU, however, patients treated with IM and carrying der(9) deletions presented better cytogenetic response. FAU - Bennour, Ayda AU - Bennour A AD - Department of Cytogenetics, Molecular Genetics and Reproductive Biology, Farhat Hached University Teaching Hospital, Sousse, Tunisia. aydabennour@yahoo.fr FAU - Ouahchi, Ines AU - Ouahchi I FAU - Ben Youssef, Yosra AU - Ben Youssef Y FAU - Zaier, Monia AU - Zaier M FAU - Laatiri, Mohamed Adnene AU - Laatiri MA FAU - Harrabi, Imed AU - Harrabi I FAU - Meddeb, Balkis AU - Meddeb B FAU - Elloumi, Moez AU - Elloumi M FAU - Khelif, Abderrahim AU - Khelif A FAU - Saad, Ali AU - Saad A FAU - Sennana, Halima AU - Sennana H LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110403 PL - United States TA - Med Oncol JT - Medical oncology (Northwood, London, England) JID - 9435512 RN - 0 (Benzamides) RN - 0 (DNA Probes) RN - 0 (Piperazines) RN - 0 (Pyrimidines) RN - 8A1O1M485B (Imatinib Mesylate) RN - EC 2.7.10.2 (Proto-Oncogene Proteins c-abl) RN - EC 2.7.11.1 (BCR protein, human) RN - EC 2.7.11.1 (Proto-Oncogene Proteins c-bcr) RN - X6Q56QN5QC (Hydroxyurea) SB - IM MH - Adult MH - Antineoplastic Combined Chemotherapy Protocols/*therapeutic use MH - Benzamides MH - *Chromosome Deletion MH - Chromosomes, Human, Pair 22/*genetics MH - Chromosomes, Human, Pair 9/*genetics MH - DNA Probes MH - Female MH - Humans MH - Hydroxyurea/administration & dosage MH - Imatinib Mesylate MH - In Situ Hybridization, Fluorescence MH - Karyotyping MH - Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy/*genetics MH - Male MH - Middle Aged MH - Philadelphia Chromosome MH - Piperazines/administration & dosage MH - Prognosis MH - Proto-Oncogene Proteins c-abl/genetics MH - Proto-Oncogene Proteins c-bcr/genetics MH - Pyrimidines/administration & dosage MH - Retrospective Studies MH - Translocation, Genetic/genetics EDAT- 2011/04/05 06:00 MHDA- 2012/09/19 06:00 CRDT- 2011/04/05 06:00 PHST- 2011/03/15 00:00 [received] PHST- 2011/03/18 00:00 [accepted] PHST- 2011/04/05 06:00 [entrez] PHST- 2011/04/05 06:00 [pubmed] PHST- 2012/09/19 06:00 [medline] AID - 10.1007/s12032-011-9918-8 [doi] PST - ppublish SO - Med Oncol. 2012 Jun;29(2):1151-60. doi: 10.1007/s12032-011-9918-8. Epub 2011 Apr 3.