Abstract
Acute myelogenous leukemia (AML) is a heterogeneous disease characterized by myeloid progenitor cells uncontrolled proliferation gradually replacing normal hematopoiesis. To evaluate Ten Eleven Translocation 2 gene (TET2) single nucleotide polymorphism (SNP) (rs2454206, rs34402524, rs61744960) in AML, and chronic myeloid leukemia (CML) in relation to their disease prognostic criteria. The study included 136 subjects; 52 AML, 54 CML and 30 subjects as control group matched for age and sex. Routine investigations including CBC, bone marrow aspiration, flow cytometry biochemical investigations and cytogenetics and molecular study were performed accordingly. DNA extraction and SNP assay for TET2 gene polymorphism was done using (Thermo-Fisher predesigned SNP, USA) PCR prism 7500. The mean age was 43.4 ± 14.0 years in AML patients, 45.98 ± 15.7 years in CML patients and 39.3 ± 6.587 years in control group (p > 0.05). The frequency of TET2 SNP rs 34402524 ranged from heterozygous to homozygous in both AML (46%, 54%) and CML (48%, 46.2%) groups but was mainly homozygous among the control (80%) group (p = 0.012). TET2 SNP rs 2454206 was mainly wild in CML (65.4%) and control (63.3%) groups compared to AML as wild was only in (46%) and heterozygous in (44%) with only 10% being homozygous (p = 0.046). TET2 SNP rs 61744960 showed a homozygous pattern among all three group (AML CML and control) showing no statistical significance (p = 0.528). Eventhough, higher non responders to treatment were among homozygous and heterozygous groups yet, response to therapy as respect to specific TET2 SNP showed no significant variation (p > 0.05). TET2 SNP in CML cases did not alter the prognostic criteria as no statistical significance was noted (p > 0.05) except for TET2 SNP rs 34402524 where homozygous cases had larger spleen size (p = 0.019). TET2 SNP is common in Egyptian myeloid neoplasm. This is the first study in this field and further studies are recommended to investigate TET2 and relation to other hematological malignancies and leukemogenesis transformation.
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All data are in the possession of corresponding author and were presented in figure and tables and materials of study were executed in both Medical Genetics Center and Clinical Pathology in Faculty of Medicine, Alexandria University.
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Acknowledgements
Special thanks to Hematology Department all physicians, nurses and paramedics whom actively participated in this work. Special thanks to the Medical Genetics Center technicians who were keen and dedicated to this work. Lastly but not least special thanks to the Clinical Pathology Department Hematology section team whose participation founded the basic steps in this work.
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ED corresponding author funded, selected patients and data, participated in the lab work for molecular study, and followed up cases after induction/remission cycle. NAMH and NAE suggested the field of research, supervised, monitored and guided the research. HSK Medical Genetics Center performed the molecular study on TET2 polymorphism. MWA Clinical Pathology performed the routine diagnostic tests including biochemical tests bone marrow aspiration immunophenotyping and cytogenetics analysis.
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Dammag, E.A., Hamed, N.A.M., Elhalawani, N.A. et al. TET2 Single Nucleotide Polymorphism in Myeloid Neoplasms Among Egyptian Patients. Indian J Hematol Blood Transfus 36, 91–96 (2020). https://doi.org/10.1007/s12288-019-01172-z
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DOI: https://doi.org/10.1007/s12288-019-01172-z