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RETRACTED ARTICLE: Detection and clinical significance of gene rearrangements in Chinese patients with adult acute lymphoblastic leukemia
- Source :
- Leukemia & Lymphoma. 54:1521-1526
- Publication Year :
- 2013
- Publisher :
- Informa UK Limited, 2013.
-
Abstract
- This study aimed to develop a novel multiplex reverse transcription-nested polymerase chain reaction (RT-nPCR) assay to accurately and effectively detect 10 common gene rearrangements in adult acute lymphoblastic leukemia (ALL) and to examine the clinicopathologic characteristics and other genetic aberrations of patients with ALL expressing different fusion genes. Our RT-nPCR assay had a positive detection rate of 35.15% (90/256) for the 10 fusion genes. BCR-ABL1, FUS-ERG, MLL-AF4, ETV6-RUNX1, E2A-PBX1, dupMLL, MLL-AF10, MLL-ENL, SET-NUP214 and SIL-TAL1 were detected in 36 (14.06%), 14 (5.47%), 14 (5.47%), four (1.56%), four (1.56%), five (1.95%), four (1.56%), two (0.78%), two (0.78%) and five patients (1.95%), respectively. The RT-nPCR results were further confirmed by split-out PCR, and cytogenetic and fluorescence in situ hybridization (FISH) analysis revealed corresponding translocations and fusions in 63 and 74 cases, respectively. JAK2 and IKZF1 mutations were commonly detected in patients with BCR-ABL1 ALL, and HOX overexpression was highly correlated with MLL fusions and SET-NUP214. This study demonstrates that RT-nPCR is an effective method for identifying 10 gene rearrangements in adult ALL, and it could potentially be developed for diagnostic use and prognostic studies of ALL.
- Subjects :
- Cancer Research
medicine.diagnostic_test
Chromosomal translocation
Hematology
Gene rearrangement
Biology
Molecular biology
law.invention
Fusion gene
Oncology
law
hemic and lymphatic diseases
medicine
Adult Acute Lymphoblastic Leukemia
Multiplex
Gene
Polymerase chain reaction
Fluorescence in situ hybridization
Subjects
Details
- ISSN :
- 10292403 and 10428194
- Volume :
- 54
- Database :
- OpenAIRE
- Journal :
- Leukemia & Lymphoma
- Accession number :
- edsair.doi...........7418e3d2105bba3d0e9516b3993b4377