Literature DB >> 16946305

JAK2(V617F): Prevalence in a large Chinese hospital population.

Xuesong Xu1, Qi Zhang, Jian Luo, Shu Xing, Qingshan Li, Sanford B Krantz, Xueqi Fu, Zhizhuang Joe Zhao.   

Abstract

Recently, the JAK2(V617F) mutation was found in patients with myeloproliferative disorders (MPDs), including most with polycythemia vera (PV). The mutant JAK2 has increased kinase activity, and it was shown to be pathogenic in mouse models. Herein, we analyzed blood samples randomly collected from a clinical laboratory. Surprisingly, as many as 37 samples from a total of 3935 were found positive for the JAK2 mutation. However, only one of these samples had blood test results indicative for probable PV, but several had nonhematologic diseases. On average, samples with the mutation had normal red cell counts but significantly higher white blood cell and platelet counts, although most were within the normal range. The data suggest that the JAK2(V617F) mutation is apparently much more common than MPDs. Its occurrence may be a prelude to full blood cell abnormalities and other diseases, but it cannot by itself diagnose MPDs.

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Year:  2006        PMID: 16946305      PMCID: PMC1785080          DOI: 10.1182/blood-2006-03-009472

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  24 in total

1.  Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia.

Authors:  P Peeters; S D Raynaud; J Cools; I Wlodarska; J Grosgeorge; P Philip; F Monpoux; L Van Rompaey; M Baens; H Van den Berghe; P Marynen
Journal:  Blood       Date:  1997-10-01       Impact factor: 22.113

2.  The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia.

Authors:  Ross L Levine; Marc Loriaux; Brian J P Huntly; Mignon L Loh; Miroslav Beran; Eric Stoffregen; Roland Berger; Jennifer J Clark; Stephanie G Willis; Kim T Nguyen; Nikki J Flores; Elihu Estey; Norbert Gattermann; Scott Armstrong; A Thomas Look; James D Griffin; Olivier A Bernard; Michael C Heinrich; D Gary Gilliland; Brian Druker; Michael W N Deininger
Journal:  Blood       Date:  2005-08-04       Impact factor: 22.113

3.  Detection of the single hotspot mutation in the JH2 pseudokinase domain of Janus kinase 2 in bone marrow trephine biopsies derived from chronic myeloproliferative disorders.

Authors:  Oliver Bock; Guntram Büsche; Christina Koop; Sabine Schröter; Thomas Buhr; Hans Kreipe
Journal:  J Mol Diagn       Date:  2006-05       Impact factor: 5.568

Review 4.  Role of tyrosine kinases and phosphatases in polycythemia vera.

Authors:  Zhizhuang Joe Zhao; William Vainchenker; Sanford B Krantz; Nicole Casadevall; Stefan N Constantinescu
Journal:  Semin Hematol       Date:  2005-10       Impact factor: 3.851

5.  Methods for the detection of the JAK2 V617F mutation in human myeloproliferative disorders.

Authors:  Peter J Campbell; Linda M Scott; E Joanna Baxter; Anthony J Bench; Anthony R Green; Wendy N Erber
Journal:  Methods Mol Med       Date:  2006

6.  The t(8;9)(p22;p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2.

Authors:  Andreas Reiter; Christoph Walz; Ann Watmore; Claudia Schoch; Ilona Blau; Brigitte Schlegelberger; Ute Berger; Nick Telford; Shilani Aruliah; John A Yin; Danny Vanstraelen; Helen F Barker; Peter C Taylor; Aisling O'Driscoll; Fabio Benedetti; Cornelia Rudolph; Hans-Jochem Kolb; Andreas Hochhaus; Rüdiger Hehlmann; Andrew Chase; Nicholas C P Cross
Journal:  Cancer Res       Date:  2005-04-01       Impact factor: 12.701

7.  Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders.

Authors:  E Joanna Baxter; Linda M Scott; Peter J Campbell; Clare East; Nasios Fourouclas; Soheila Swanton; George S Vassiliou; Anthony J Bench; Elaine M Boyd; Natasha Curtin; Mike A Scott; Wendy N Erber; Anthony R Green
Journal:  Lancet       Date:  2005 Mar 19-25       Impact factor: 79.321

8.  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

Review 9.  Jak family of kinases in cancer.

Authors:  Amit Verma; Suman Kambhampati; Simrit Parmar; Leonidas C Platanias
Journal:  Cancer Metastasis Rev       Date:  2003-12       Impact factor: 9.264

10.  Expression of Jak2V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model.

Authors:  Gerlinde Wernig; Thomas Mercher; Rachel Okabe; Ross L Levine; Benjamin H Lee; D Gary Gilliland
Journal:  Blood       Date:  2006-02-14       Impact factor: 22.113

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  40 in total

1.  High resolution melting analysis for JAK2 Exon 14 and Exon 12 mutations: a diagnostic tool for myeloproliferative neoplasms.

Authors:  Inmaculada Rapado; Silvia Grande; Enriqueta Albizua; Rosa Ayala; José-Angel Hernández; Miguel Gallardo; Florinda Gilsanz; Joaquin Martinez-Lopez
Journal:  J Mol Diagn       Date:  2009-03       Impact factor: 5.568

2.  Somatic and germline genetics at the JAK2 locus.

Authors:  Peter J Campbell
Journal:  Nat Genet       Date:  2009-04       Impact factor: 38.330

3.  Detection of exon 12 Mutations in the JAK2 gene: enhanced analytical sensitivity using clamped PCR and nucleotide sequencing.

Authors:  Todd S Laughlin; Alison R Moliterno; Brady L Stein; Paul G Rothberg
Journal:  J Mol Diagn       Date:  2010-03-04       Impact factor: 5.568

4.  Sensitive detection and quantification of the JAK2V617F allele by real-time PCR blocking wild-type amplification by using a peptide nucleic acid oligonucleotide.

Authors:  Cornelis J J Huijsmans; Jeroen Poodt; Paul H M Savelkoul; Mirjam H A Hermans
Journal:  J Mol Diagn       Date:  2011-06-30       Impact factor: 5.568

Review 5.  Ethical considerations in genomic testing for hematologic disorders.

Authors:  Jonathan M Marron; Steven Joffe
Journal:  Blood       Date:  2017-06-09       Impact factor: 22.113

6.  Budd-Chiari Syndrome in a Patient with JAK-2 V617F and Factor V G1691A Mutations.

Authors:  J S Velarde-Félix; J Sanchez-Zazueta; F P Gonzalez-Ibarra; J A González-Valdez; B Salcido-Gómez; E Gallardo-Angulo; J Murillo-Llanes
Journal:  West Indian Med J       Date:  2014-06-10       Impact factor: 0.171

Review 7.  Underlying mechanisms of the JAK2V617F mutation in the pathogenesis of myeloproliferative neoplasms.

Authors:  A Mullally
Journal:  Pathologe       Date:  2016-11       Impact factor: 1.011

8.  Characterization of a highly effective protein substrate for analysis of JAK2(V617F) Activity.

Authors:  Zhe Li; Shu Xing; Shaofeng Wang; Wanting Tina Ho; Zhizhuang Joe Zhao
Journal:  Exp Hematol       Date:  2007-08-30       Impact factor: 3.084

9.  Prevalence of the frequency of JAK2 (V617F) mutation in different myeloproliferative disorders in Egyptian patients.

Authors:  Gamal T Ebid; Mohamed Ghareeb; Omina Salaheldin; Mahmoud M Kamel
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01

10.  Mesenteric venous thrombosis secondary to an unsuspected JAK2 V617F-positive myeloproliferative disorder.

Authors:  M G Bourke; S T Martin; M O'Dwyer; J Hanaghan; F Bennani; M K Barry
Journal:  Ir J Med Sci       Date:  2009-08-20       Impact factor: 1.568

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