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Detection of complex karyotype in a myelodysplastic syndrome cell line (MUTZ-1) by metaphase fluorescence in situ hybridization / 中国实验血液学杂志
Article de En | WPRIM | ID: wpr-280736
Bibliothèque responsable: WPRO
ABSTRACT
This study was aimed to investigate the cytogenetic changes of MDS cell line (MUTZ-1) with chromosome 5q deletion. R-banding analysis was used to identify chromosome aberrations in MDS cell line and Vysis Spectra Vysion M-FISH was used to further characterize chromosomal complex karyotype. The results indicated that M-FISH exhibited obvious chromosomal aberrations with high frequency including translocation, insertion, breakage and rearrangement, deletion and increasement of chromosome number, the complex karyotype of MUTZ-1 was shown as 50, xx, der (1) t (1;2), ins (1;14), +der (2) t(2;19), der (3) t (3;5), der (3) (3::5::22), 5q-, der (6) t (3;6), der (7) (18::7::17), +8, +der (9) t (1;9), der (10) t (1;10), +11, +12, der (?13) (10::13::5::8), der (14) t (8;14), der (14) t (14, 15), der (15) t (15;21) x 2, +17, +18, -21, -22. It is concluded that M-FISH analysis revealed obvious changes in complex karyotype of MDS cell line MUTZ-1, and the M-FISH technique can increase accuracy of detection for chromosomal complex karyotype, and help diagnosis and prognostic evaluation of MDS.
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Translocation génétique / Syndromes myélodysplasiques / Chromosomes humains de la paire 5 / Cellules cancéreuses en culture / Aberrations des chromosomes / Délétion de segment de chromosome / Hybridation fluorescente in situ / Génétique / Caryotypage / Méthodes Type d'étude: Diagnostic_studies Limites du sujet: Child, preschool / Female / Humans langue: En Texte intégral: Journal of Experimental Hematology Année: 2006 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Translocation génétique / Syndromes myélodysplasiques / Chromosomes humains de la paire 5 / Cellules cancéreuses en culture / Aberrations des chromosomes / Délétion de segment de chromosome / Hybridation fluorescente in situ / Génétique / Caryotypage / Méthodes Type d'étude: Diagnostic_studies Limites du sujet: Child, preschool / Female / Humans langue: En Texte intégral: Journal of Experimental Hematology Année: 2006 Type: Article