The JAK2 V617F mutation in de novo acute myelogenous leukemias
A missense somatic mutation in JAK2 gene ( JAK2 V617F) has recently been reported in chronic myeloproliferative disorders, including polycythemia vera, essential thrombocythemia and myelofibrosis with myeloid metaplasia, strongly suggesting its role in the pathogenesis of myeloid disorders. As activ...
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Published in | Oncogene Vol. 25; no. 9; pp. 1434 - 1436 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
02.03.2006
Nature Publishing Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 0950-9232 1476-5594 |
DOI | 10.1038/sj.onc.1209163 |
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Summary: | A missense somatic mutation in
JAK2
gene (
JAK2
V617F) has recently been reported in chronic myeloproliferative disorders, including polycythemia vera, essential thrombocythemia and myelofibrosis with myeloid metaplasia, strongly suggesting its role in the pathogenesis of myeloid disorders. As activation of JAK2 signaling is occurred in other malignancies as well, we have analysed 558 tissues from common human cancers, including colon, breast and lung carcinomas, and 143 acute adulthood leukemias by polymerase chain reaction – single strand conformation polymorphism analysis. We found three
JAK2
mutations in the 113 acute myelogenous leukemias (AMLs) (2.7%), but none in other cancers. The mutations consisted of two V617F mutations and one K607N mutation. None of the AML patients with the
JAK2
V617F mutation had a history of previous hematologic disorders. This is the first report on the
JAK2
gene mutation in AML, and the data indicated that the
JAK2
gene mutation may not only contribute to the development of chronic myeloid disorders, but also to some AMLs. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0950-9232 1476-5594 |
DOI: | 10.1038/sj.onc.1209163 |