Literature DB >> 17440677

Incidence and significance of the JAK2 V617F mutation in patients with chronic myeloproliferative disorders.

S E Langabeer1, F Ni Ainle, E Conneally, M Lawler.   

Abstract

BACKGROUND: The chronic myeloproliferative disorders (MPD) are clonal haemopoietic stem cell disorders. AIMS: The incidence of JAK2 V617F mutation was sought in a population of patients with MPD.
METHODS: The JAK2 V617 mutation status was determined in 79 patients with known MPD and 59 patients with features suggestive of MPD.
RESULTS: The mutation was found in patients with polycythaemia vera, essential thrombocythaemia, idiopathic myelofibrosis and in patients with other chronic myeloproliferative disorders. Eight JAK2 V617F positive cases were identified amongst those patients with features suggestive of MPD.
CONCLUSIONS: The incidence of the JAK2 V617F mutation in MPD patients is similar to that reported by other groups. The assay confirmed and refined the diagnosis of several patients with features indicative of MPD. We suggest screening for this mutation in all patients with known and suspected MPD as identification is valuable in classification and is a potential target for signal transduction therapy.

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Year:  2007        PMID: 17440677     DOI: 10.1007/s11845-007-0026-x

Source DB:  PubMed          Journal:  Ir J Med Sci        ISSN: 0021-1265            Impact factor:   1.568


  34 in total

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Authors:  I Melzner; M A Weniger; C K Menz; P Möller
Journal:  Leukemia       Date:  2006-01       Impact factor: 11.528

2.  Chronic neutrophilic leukemia with an associated V617F JAK2 tyrosine kinase mutation.

Authors:  Donald P Mc Lornan; Melanie J Percy; Amy V Jones; Nicholas C P Cross; Mary Frances Mc Mullin
Journal:  Haematologica       Date:  2005-12       Impact factor: 9.941

3.  The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera.

Authors:  Ayalew Tefferi; Terra L Lasho; Susan M Schwager; Jacob S Strand; Michelle Elliott; Ruben Mesa; Chin-Yang Li; Martha Wadleigh; Stephanie J Lee; D Gary Gilliland
Journal:  Cancer       Date:  2006-02-01       Impact factor: 6.860

4.  The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders.

Authors:  Linda M Scott; Peter J Campbell; E Joanna Baxter; Tony Todd; Philip Stephens; Sarah Edkins; Richard Wooster; Michael R Stratton; P Andrew Futreal; Anthony R Green
Journal:  Blood       Date:  2005-10-15       Impact factor: 22.113

5.  Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.

Authors:  Ross L Levine; Martha Wadleigh; Jan Cools; Benjamin L Ebert; Gerlinde Wernig; Brian J P Huntly; Titus J Boggon; Iwona Wlodarska; Jennifer J Clark; Sandra Moore; Jennifer Adelsperger; Sumin Koo; Jeffrey C Lee; Stacey Gabriel; Thomas Mercher; Alan D'Andrea; Stefan Fröhling; Konstanze Döhner; Peter Marynen; Peter Vandenberghe; Ruben A Mesa; Ayalew Tefferi; James D Griffin; Michael J Eck; William R Sellers; Matthew Meyerson; Todd R Golub; Stephanie J Lee; D Gary Gilliland
Journal:  Cancer Cell       Date:  2005-04       Impact factor: 31.743

6.  Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders.

Authors:  Amy V Jones; Sebastian Kreil; Katerina Zoi; Katherine Waghorn; Claire Curtis; Lingyan Zhang; Joannah Score; Rachel Seear; Andrew J Chase; Francis H Grand; Helen White; Christine Zoi; Dimitris Loukopoulos; Evangelos Terpos; Elisavet-Christine Vervessou; Beate Schultheis; Michael Emig; Thomas Ernst; Eva Lengfelder; Rüdiger Hehlmann; Andreas Hochhaus; David Oscier; Richard T Silver; Andreas Reiter; Nicholas C P Cross
Journal:  Blood       Date:  2005-05-26       Impact factor: 22.113

Review 7.  Molecular monitoring of BCR-ABL as a guide to clinical management in chronic myeloid leukaemia.

Authors:  Timothy Hughes; Susan Branford
Journal:  Blood Rev       Date:  2005-03-02       Impact factor: 8.250

8.  Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies.

Authors:  Anthony J Bench; Juan Li; Brian J P Huntly; Eric Delabesse; Nasios Fourouclas; Adrienne R Hunt; Panos Deloukas; Anthony R Green
Journal:  Br J Haematol       Date:  2004-12       Impact factor: 6.998

Review 9.  Standardized RT-PCR analysis of fusion gene transcripts from chromosome aberrations in acute leukemia for detection of minimal residual disease. Report of the BIOMED-1 Concerted Action: investigation of minimal residual disease in acute leukemia.

Authors:  J J van Dongen; E A Macintyre; J A Gabert; E Delabesse; V Rossi; G Saglio; E Gottardi; A Rambaldi; G Dotti; F Griesinger; A Parreira; P Gameiro; M G Diáz; M Malec; A W Langerak; J F San Miguel; A Biondi
Journal:  Leukemia       Date:  1999-12       Impact factor: 11.528

10.  JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia.

Authors:  Jaroslav Jelinek; Yasuhiro Oki; Vazganush Gharibyan; Carlos Bueso-Ramos; Josef T Prchal; Srdan Verstovsek; Miloslav Beran; Elihu Estey; Hagop M Kantarjian; Jean-Pierre J Issa
Journal:  Blood       Date:  2005-07-21       Impact factor: 22.113

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  4 in total

1.  Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential thrombocythemia and polycythemia vera.

Authors:  Mutlu Karkucak; Tahsin Yakut; Vildan Ozkocaman; Fahir Ozkalemkas; Ridvan Ali; Murat Bayram; Orhan Gorukmez; Gokhan Ocakoglu
Journal:  Mol Biol Rep       Date:  2012-06-22       Impact factor: 2.316

2.  Evaluation of clinical and laboratory findings with JAK2 V617F mutation as an independent variable in essential thrombocytosis.

Authors:  Güven Cetin; Tuba Ozkan; Seda Turgut; M Ali Cikrikcioglu; M Cem Ar; Mesut Ayer; Ayhan Unlu; Sevda Rabia Celik; Yahya Sekin; Cumali Karatoprak
Journal:  Mol Biol Rep       Date:  2014-07-11       Impact factor: 2.316

3.  The role of genotypes that modify the toxicity of chemical mutagens in the risk for myeloproliferative neoplasms.

Authors:  Carol Ann Gross-Davis; Karyn Heavner; Arthur L Frank; Craig Newschaffer; Judith Klotz; Regina M Santella; Igor Burstyn
Journal:  Int J Environ Res Public Health       Date:  2015-02-24       Impact factor: 3.390

4.  Triple-Negative Essential Thrombocythemia Complicated by Thrombosis and Acquired von Willebrand Disease in a Young Man.

Authors:  Tejaswi Kanderi; Max Puthenpura; Isha Shrimanker; Fnu Sapna; Scott C Felter
Journal:  Am J Case Rep       Date:  2020-08-23
  4 in total

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