S. Polampalli, P. Amre, S. Shinde, S. Banavali, K. Prabhash, R. , Nair, P.G. Subramanian, S. Gujral, P.M. Parikh
Published: January 05, 2009
Genet. Mol. Res. 8 (1) : 1-7
DOI: https://doi.org/10.4238/vol8-1gmr488
Cite this Article:
A. Choughule, S. Polampalli, P. Amre, S. Shinde, S. Banavali, K. Prabhash, R. Nair, P.G. Subramanian, S. Gujral, P.M. Parikh (2009). Identification of PML/RARα fusion gene transcripts that showed no t(15;17) with conventional karyotyping and fluorescent in situ hybridization. Genet. Mol. Res. 8(1): 1-7. https://doi.org/10.4238/vol8-1gmr488, Vitis vinifera.
About the Authors
S. Polampalli, P. Amre, S. Shinde, S. Banavali, K. Prabhash, R. , Nair, P.G. Subramanian, S. Gujral, P.M. Parikh
Corresponding author
A. Choughule
E-mail: anu.c1112@gmail.com
ABSTRACT
Acute promyelocytic leukemia (APL) is characterized by a reciprocal translocation, t(15;17)(q22;q11-21), resulting in the fusion of the promyelocytic leukemia (PML) and retinoic acid receptor alpha (RARα) genes. Using conventional cytogenetic methods, these translocations are normally detected in about 70-90% of patients; most negative results are due to technical problems or cryptic variants. These masked PML/RARα fusions can be identified by molecular analyses, such as reverse transcriptase-polymerase chain reaction (RT-PCR) or fluorescence in situ hybridization (FISH). Approximately 5 to 10% of all APL cases reported do not show PML/RARα fusion transcripts, even with dual-colored FISH. We report three of 40 diagnosed APL cases that showed morphological, cytochemical, and immunophenotypic features of hypergranular APL, but did not show a PML/RARα fusion signal or any of its variants, on FISH. All cases were identified by RT-PCR, which was further confirmed by cDNA sequencing. Conventional karyotyping showed other clonal aberrations in these cases, but failed to show t(15;17) or any other variants or complex translocations.
Key words: Fluorescence in situ hybridization, Acute promyelocytic leukemia, Cryptic insertions, promyelocytic leukemia/retinoic acid receptor alpha, Reverse transcription-polymerase chain reaction, Sequencing analysis.