Literature DB >> 18048969

Detection of the JAK2V617F mutation by asymmetric PCR and melt curve analysis.

Bobbie Collett Sutton1, Richard A Allen, Zhizhuang Joe Zhao, S Terence Dunn.   

Abstract

The chronic myeloproliferative disorders (CMPDs) are a heterogeneous group of clonal hematopoietic diseases characterized by production of increased numbers of mature leukocytes, erythrocytes, and/or platelets. Clinically these disorders are often insidious in onset, produce nonspecific thrombotic or hemorrhagic complications, and can be easily confused with a variety of benign, reactive conditions. Thus, confirming a CMPD can be difficult as it is often a diagnosis of exclusion. The recently identified JAK2(V617F) mutation is frequently present in the classic CMPDs polycythemia vera, essential thrombocythemia, and chronic idiopathic myelofibrosis. JAK2(V617F) determination has proven to be a useful diagnostic tool in patients with some clinical features suggestive for a CMPD, and may have benefit as a way to monitor known disease. There are several published molecular assays for the JAK2(V617F) target, of variable sensitivity and technical complexity, many of which are not easily replicated in a typical clinical laboratory. We present a robust, sensitive PCR/melt curve assay for the JAK2(V617F) mutation which uses the widely available Roche LightCycler platform, and is thus applicable to many clinical molecular laboratories.

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Year:  2007        PMID: 18048969     DOI: 10.3233/cbm-2007-3605

Source DB:  PubMed          Journal:  Cancer Biomark        ISSN: 1574-0153            Impact factor:   4.388


  8 in total

1.  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

2.  A real-time polymerase chain reaction assay for rapid, sensitive, and specific quantification of the JAK2V617F mutation using a locked nucleic acid-modified oligonucleotide.

Authors:  Barbara Denys; Hakim El Housni; Friedel Nollet; Bruno Verhasselt; Jan Philippé
Journal:  J Mol Diagn       Date:  2010-04-29       Impact factor: 5.568

3.  Thrombophilic factor analysis in cirrhotic patients with portal vein thrombosis.

Authors:  Bernd Saugel; Marcel Lee; Stephanie Feichtinger; Alexander Hapfelmeier; Roland M Schmid; Jens T Siveke
Journal:  J Thromb Thrombolysis       Date:  2015-07       Impact factor: 2.300

4.  Melting point assay for the JAK2 V617F mutation, comparison with amplification refractory mutation system (ARMS) in diagnostic samples, and implications for daily routine.

Authors:  Sebastian Ochsenreither; Mark Reinwald; Eckhard Thiel; Thomas Burmeister
Journal:  Mol Diagn Ther       Date:  2010-06-01       Impact factor: 4.074

5.  Neutrophils use selective autophagy receptor Sqstm1/p62 to target Staphylococcus aureus for degradation in vivo in zebrafish.

Authors:  Josie F Gibson; Tomasz K Prajsnar; Christopher J Hill; Amy K Tooke; Justyna J Serba; Rebecca D Tonge; Simon J Foster; Andrew J Grierson; Philip W Ingham; Stephen A Renshaw; Simon A Johnston
Journal:  Autophagy       Date:  2020-06-19       Impact factor: 16.016

6.  Development of a highly sensitive method for detection of JAK2V617F.

Authors:  Anna H Zhao; Rufei Gao; Zhizhuang J Zhao
Journal:  J Hematol Oncol       Date:  2011-10-10       Impact factor: 17.388

7.  JAK2V617F and p53 mutations coexist in erythroleukemia and megakaryoblastic leukemic cell lines.

Authors:  Wanke Zhao; Yanhong Du; Wanting Tina Ho; Xueqi Fu; Zhizhuang Joe Zhao
Journal:  Exp Hematol Oncol       Date:  2012-06-21

8.  Quantitative threefold allele-specific PCR (QuanTAS-PCR) for highly sensitive JAK2 V617F mutant allele detection.

Authors:  Giada V Zapparoli; Robert N Jorissen; Chelsee A Hewitt; Michelle McBean; David A Westerman; Alexander Dobrovic
Journal:  BMC Cancer       Date:  2013-04-24       Impact factor: 4.430

  8 in total

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