Analysis of class I and II aberrations in Iraqi childhood acute myeloid leukemia using filter paper cards
Autor: | Jaafar M.H. Abdulkadhim, Lika’a Fasih Y. Al-Kzayer, Le T.N. Uyen, M. Al-Ani, Hasanein H. Ghali, Salma Abbas Al-Hadad, Tariq Abadi Al-Shujairi, Zead Ismael I.K. Matti, Najiha Ahmed Ameen, Mazin Faisal Al-Jadiry, Toshi Inoshita, Paiman Ali I. Saber, Hussam M. Salih Al-Abdullah, Kenichi Koike, Hisham Maree Khalil, Janan Ghalib Hasan, Safaa A. F. Al‐Badri, Kazuyuki Matsuda, Minoru Kamata, Tingting Liu, Kazuo Sakashita |
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Rok vydání: | 2014 |
Předmět: |
Male
Paper Acute promyelocytic leukemia Oncology NPM1 medicine.medical_specialty Adolescent Oncogene Proteins Fusion medicine.medical_treatment Hematopoietic stem cell transplantation Genetic analysis Leukemia Myelomonocytic Acute Translocation Genetic Specimen Handling Bone Marrow hemic and lymphatic diseases Internal medicine medicine Humans Child Alleles Chromosome Aberrations Blood Specimen Collection Hematology Reverse Transcriptase Polymerase Chain Reaction business.industry Childhood Acute Myeloid Leukemia Infant Cancer DNA Neoplasm Oncogenes Sequence Analysis DNA General Medicine Prognosis medicine.disease Leukemia Myeloid Acute Treatment Outcome medicine.anatomical_structure Child Preschool Iraq Mutation Immunology Female Bone marrow business Nucleophosmin |
Zdroj: | Annals of Hematology. 93:949-955 |
ISSN: | 1432-0584 0939-5555 |
DOI: | 10.1007/s00277-014-2007-2 |
Popis: | The lack of molecular diagnosis in the field of cancer in Iraq has motivated us to perform a genetic analysis of pediatric acute myelogenous leukemia (AML), including class I and II aberrations. Peripheral blood or bone marrow cells were collected from 134 AML children aged ≤15 years. Flinders Technology Associates (FTA) filter paper cards were used to transfer dried blood samples from five Iraqi hospitals to Japan. DNA sequencing was performed to identify class I mutations. Nested RT-PCR was used to detect class II aberrations, except that MLL rearrangement was detected according to long distance inverse-PCR. NPM1 and FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) mutations were analyzed by GeneScan using DNA template. Among 134 Iraqi pediatric AML samples, the most prevalent FAB subtype was M2 (33.6 %) followed by M3 (17.9 %). Class I mutations: 20 (14.9 %), 8 (6.0 %), and 8 (6.0 %) patients had FLT3-ITD, FLT3-TKD, and KIT mutations, respectively. Class II mutations: 24 (17.9 %), 19 (14.2 %), and 9 (6.7 %) children had PML-RARA, RUNX1-RUNX1T1, and CBFB-MYH11 transcripts, respectively. MLL rearrangements were detected in 25 (18.7 %) patients. NPM1 mutation was detected in seven (5.2 %) cases. Collectively, approximately 30 % of AML children were proved to carry favorable prognostic genetic abnormalities, whereas approximately 10 % had high FLT3-ITD allelic burden and needed a special treatment plan including allogeneic hematopoietic stem cell transplantation. Acute promyelocytic leukemia (APL) was frequent among Iraqi pediatric AML. It is likely that molecular diagnosis using FTA cards in underdeveloped countries could guide doctors towards an appropriate treatment strategy. |
Databáze: | OpenAIRE |
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