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
Journal of Experimental Hematology
; (6): 46-49, 2006.
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.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Translocation génétique
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Syndromes myélodysplasiques
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Chromosomes humains de la paire 5
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Cellules cancéreuses en culture
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Aberrations des chromosomes
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Délétion de segment de chromosome
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Hybridation fluorescente in situ
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Génétique
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Caryotypage
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Méthodes
Type d'étude:
Diagnostic_studies
Limites du sujet:
Child, preschool
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Female
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Humans
langue:
En
Texte intégral:
Journal of Experimental Hematology
Année:
2006
Type:
Article