Detection of the complex chromosomal aberrations in acute lymphoblastic leukemia by means of multiplex fluorescence in situ hybridization.
- Author:
Jian-Yong LI
1
;
Li MA
;
Bing XIAO
;
Jin-Lan PAN
;
Hai-Rong QIU
;
Ya-Fang WU
;
Bing-Zhao WEN
;
Yong-Quan XUE
Author Information
1. Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China. lijianyonglm@medmail.com.cn
- Publication Type:Journal Article
- MeSH:
Adolescent;
Adult;
Chromosome Aberrations;
Cytogenetic Analysis;
Female;
Humans;
In Situ Hybridization, Fluorescence;
methods;
Karyotyping;
Male;
Middle Aged;
Precursor Cell Lymphoblastic Leukemia-Lymphoma;
genetics
- From:
Journal of Experimental Hematology
2006;14(1):42-45
- CountryChina
- Language:Chinese
-
Abstract:
This study was aimed to establish the technique of multiplex fluorescence in situ hybridization (M-FISH) and to explore its usefulness in detection of complex chromosomal aberrations (CCAs) in acute lymphoblastic leukemia (ALL). Five ALL patients with CCAs were analyzed by combining the techniques of conventional cytogenetics (CC) and M-FISH. The results demonstrated that M-FISH confirmed the aberrations previously detected by CC, such as t (9;22), t (1;19) and t (y;1), and revealed new abnormalities as der (1) (1::3::7), der (6) t (6;9) (q?;p13), der (1) t (1;11), der (12) t (1;12), der (3) t (3;5), der (2) t (2;16), der (9) (9::18::7) and der (7) (9::18::7), and also corrected the wrong results in CC. Among these abnormalities, der (9) (9::18::7) and der (7) (9::18::7) were reported for the first time. In conclusion, M-FISH has proved to be useful in characterization of the CCAs in ALL, and it is an essential method to refine the karyotype analysis.
