Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies
| العنوان: | Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies |
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| المؤلفون: | Walid Sabri Hamadou, Yosra Ben Youssef, Paul Gesta, Aurelie Fabre, Abderrahim Khelif, Testsuro Noguchi, François Eisinger, Mohamed Adnène Laatiri, Zohra Soua, Hélène Dreyfus, Sawsen Besbes, Véronique Mari, Laurence Faivre, Hagay Sobol, Pascaline Gaildrat, Hélène Zattara, Violaine Bourdon, Saloua Yacoub Jemni, Catherine Dugast, Valérie Bonadona, H. Regaieg |
| المصدر: | Annals of Hematology. 95:1043-1050 |
| بيانات النشر: | Springer Science and Business Media LLC, 2016. |
| سنة النشر: | 2016 |
| مصطلحات موضوعية: | Adult, Male, Candidate gene, NPM1, Adolescent, Acute myeloblastic leukemia, DNA Mutational Analysis, Biology, Germline, Cohort Studies, 03 medical and health sciences, Exon, 0302 clinical medicine, hemic and lymphatic diseases, Genetic predisposition, medicine, Humans, Proto-Oncogene Proteins c-cbl, Aged, Genetics, Genetic Variation, Nuclear Proteins, Family aggregation, Hematology, General Medicine, Janus Kinase 2, Middle Aged, medicine.disease, Pedigree, Hematologic Neoplasms, 030220 oncology & carcinogenesis, Core Binding Factor Alpha 2 Subunit, Cancer research, Female, Nucleophosmin, 030215 immunology, Minigene |
| الوصف: | Familial aggregation of hematological malignancies has been reported highlighting inherited genetic predisposition. In this study, we targeted four candidate genes: JAK2 and RUNX1 genes assuring a prominent function in hematological process and CBL and NPM1 as proto-oncogenes. Their disruption was described in several sporadic hematological malignancies. The aim of this study is to determine whether JAK2, CBL, RUNX1, and NPM1 germline genes mutations are involved in familial hematological malignancies. Using direct sequencing, we analyzed JAK2 (exons 12 and 14); CBL (exons 7, 8 and 9); NPM1 (exon 12) and the entire RUNX1 in 88 independent families belonging to Tunisian and French populations. Twenty-one sporadic acute leukemias were included in this study. We reported a heterozygous intronic c.1641 + 6 T > C JAK2 variant (rs182123615) found in two independent familial cases diagnosed with gastric lymphoma and Hodgkin lymphoma. The in silico analysis suggested a potential impact on splicing, but the functional splicing minigene reporter assay on rs182123615 variant showed no aberrant transcripts. In one sporadic acute myeloblastic leukemia, we reported an insertion 846 in. TGTT in exon 12 of NPM1 gene that may impact the normal reading frame. The rs182123615 JAK2 variant was described in several contexts including myeloproliferative neoplasms and congenital erythrocytosis and was supposed to be pathogenic. Through this current study, we established the assessment of pathogenicity of rs182123615 and we classified it rather as rare polymorphism. |
| تدمد: | 1432-0584 0939-5555 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::371a1460270631669f693dd47f4fbe09Test https://doi.org/10.1007/s00277-016-2678-yTest |
| حقوق: | CLOSED |
| رقم الانضمام: | edsair.doi.dedup.....371a1460270631669f693dd47f4fbe09 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 14320584 09395555 |
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