Objectives To study the FLT3 gene expression and its internal tandem duplication in malignant hematopoietic diseases and its clinical significance.Methods PCR and DNA sequencing were used to detect the FLT3/ITD mutation in blast cell of bone marrow from 86 patients with malignant hematopoietic diseases, including 32 acute myeoloid leukemia( AML) cases, 18 acute lympoid leukemia(ALL) cases, 2 acute hybrid leukemia (AHL) cases , 12 myelodys plastic syndromes (MDS) cases , 10 chronic myelogenous leukemia (CML) cases, 3 non-Hodgkin's lymphoma (NHL) cases and 9 multiple myeloma (MM) cases.Results The expression of FLT3/ITD gene were detected in 5 of 32 (15.6%) AML patients, including 1/7 of M3, 1/10 of M4 and 3/10 of M5. More FLT3 aberrations were found in AML M5. No FLT3/ITD was found in 18 ALL, 2 AHL, 12 MDS and 10 CML cases. No FLT3 was found in 3 NHL and 9 MM ases. Sequence analysis of 2 case with abnormal PCR electrophoretic patterns revealed that the ITDs was located within exon 14 from 27 to 63 bp, the ITD was a simple tandem duplication, and it did not altered the reading frame. FLT3/ITD was associated with a higher peripheral white cell count (P<0.01) and a higher percentage of bone marrow blast cells(P<0.01) and a lower complete mission rate tendency.Conclusion More FLT3/ITD mutation occurs in AML M5 patients. Sequence of the mutants was in frame mutation. FLT3/ITD mutation was associated with a higher peripheral white cell count and a higher percentage of bone marrow blast cells and a lower complete remission rate tendency.
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