Integrated genomic analysis illustrates the central role of JAK-STAT pathway activation in myeloproliferative neoplasm pathogenesis Journal Article


Authors: Rampal, R.; Al-Shahrour, F.; Abdel-Wahab, O.; Patel, J. P.; Brunel, J. P.; Mermel, C. H.; Bass, A. J.; Pretz, J.; Ahn, J.; Hricik, T.; Kilpivaara, O.; Wadleigh, M.; Busque, L.; Gilliland, D. G.; Golub, T. R.; Ebert, B. L.; Levine, R. L.
Article Title: Integrated genomic analysis illustrates the central role of JAK-STAT pathway activation in myeloproliferative neoplasm pathogenesis
Abstract: Genomic studies have identified somatic alterations in the majority of myeloproliferative neoplasms (MPN) patients, including JAK2 mutations in the majority of MPN patients and CALR mutations in JAK2-negative MPN patients. However, the role of JAK-STAT pathway activation in different MPNs, and in patients without JAK2 mutations, has not been definitively delineated. We used expression profiling, single nucleotide polymorphism arrays, and mutational profiling to investigate a well-characterized cohort of MPN patients. MPN patients with homozygous JAK2V617F mutations were characterized by a distinctive transcriptional profile. Notably, a transcriptional signature consistent with activated JAK2 signaling is seen in all MPN patients regardless of clinical phenotype or mutational status. In addition, the activated JAK2 signature was present in patients with somatic CALR mutations. Conversely, we identified a gene expression signature of CALR mutations; this signature was significantly enriched in JAK2-mutant MPN patients consistent with a shared mechanism of transformation by JAK2 and CALR mutations. We also identified a transcriptional signature of TET2 mutations in MPN patent samples. Our data indicate that MPN patients, regardless of diagnosis or JAK2 mutational status, are characterized by a distinct gene expression signature with upregulation of JAK-STAT target genes, demonstrating the central importance of the JAK-STAT pathway in MPN pathogenesis. © 2014 by The American Society of Hematology.
Keywords: signal transduction; controlled study; gene mutation; human cell; major clinical study; single nucleotide polymorphism; phenotype; gene expression profiling; cohort analysis; enzyme activation; enzyme activity; mutational analysis; genome analysis; janus kinase; nucleotide sequence; upregulation; malignant transformation; myeloproliferative neoplasm; stat protein; calreticulin; human; male; female; priority journal; article
Journal Title: Blood
Volume: 123
Issue: 22
ISSN: 0006-4971
Publisher: American Society of Hematology  
Date Published: 2014-05-29
Start Page: e123
End Page: e133
Language: English
DOI: 10.1182/blood-2014-02-554634
PROVIDER: scopus
PMCID: PMC4041169
PUBMED: 24740812
DOI/URL:
Notes: Blood -- Export Date: 8 July 2014 -- CODEN: BLOOA -- Molecular Sequence Numbers: GENBANK: GSE54646; -- Source: Scopus
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  1. Raajit Kumar Rampal
    338 Rampal
  2. Ross Levine
    775 Levine