Reverse transcription polymerase chain reaction for the diagnosis and molecular monitoring of the PML/RARα fusion gene in acute promyelocytic leukemia

Acute promyelocytic leukemia (APL) is characterized by a specific t(15;17) translocation and a high rate of response to all-trans retinoic acid. The translocation generates a PML/RARα chimeric gene which is transcribed in a fusion PML/RARα mRNA. In this study, by using RT-PCR, we examined 14 APL pat...

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Veröffentlicht in:Cancer genetics and cytogenetics 1995-10, Vol.84 (2), p.91-94
Hauptverfasser: Viniou, Nora-Athina, Yataganas, Xenophon, Stamatopoulos, Kostas, Xefteri, Ilektra, Kalmantis, Themis, Papasavas, Pantelis, Mitsulis, Chrisanthi, Rombos, John, Meletis, John, Bourantas, Kostas, Zoumbos, Nickos, Pangalis, Gerassimos, Loukopoulos, Dimitris
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Sprache:eng
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Zusammenfassung:Acute promyelocytic leukemia (APL) is characterized by a specific t(15;17) translocation and a high rate of response to all-trans retinoic acid. The translocation generates a PML/RARα chimeric gene which is transcribed in a fusion PML/RARα mRNA. In this study, by using RT-PCR, we examined 14 APL patients for PML/RARα fusion gene transcripts. Eight patients were studied at diagnosis, 2 at relapse, 1 both at relapse and after reinduction, 1 both at diagnosis and after three cycles of consolidation chemotherapy, and 2 patients were examined for minimal residual disease (MRD) 4 months after completing treatment. A positive result was observed in all 14 cases. Two patients who were in complete hematologic remission had evidence of hematologic relapse soon after the positive test. We conclude that RT-PCR for APL yields important diagnostic and prognostic information for the APL patients.
ISSN:0165-4608
1873-4456
DOI:10.1016/0165-4608(95)00093-3