4.6 Review

Roles of JAK2 in Aging, Inflammation, Hematopoiesis and Malignant Transformation

Journal

CELLS
Volume 8, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/cells8080854

Keywords

JAK2; Janus-kinase; aging; clonal hematopoiesis (CHIP); myeloproliferative neoplasia (MPN)

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Funding

  1. Thuringian Ministry for Research [FSU-I-03/14]
  2. German Research Council (DFG) [HE 6233/4-1]

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Clonal alterations in hematopoietic cells occur during aging and are often associated with the establishment of a subclinical inflammatory environment. Several age-related conditions and diseases may be initiated or promoted by these alterations. JAK2 mutations are among the most frequently mutated genes in blood cells during aging. The most common mutation within the JAK2 gene is JAK2-V617F that leads to constitutive activation of the kinase and thereby aberrant engagement of downstream signaling pathways. JAK2 mutations can act as central drivers of myeloproliferative neoplasia, a pre-leukemic and age-related malignancy. Likewise, hyperactive JAK-signaling is a hallmark of immune diseases and critically influences inflammation, coagulation and thrombosis. In this review we aim to summarize the current knowledge on JAK2 in clonal hematopoiesis during aging, the role of JAK-signaling in inflammation and lymphocyte biology and JAK2 function in age-related diseases and malignant transformation.

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