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Molecular Pathogenesis of Myeloproliferative Neoplasms.

AbstractPURPOSE OF REVIEW:
Myeloproliferative neoplasms (MPNs) are chronic hematological malignancies characterized by increased proliferation of MPN stem and myeloid progenitor cells with or without bone marrow fibrosis that typically lead to increased peripheral blood cell counts. The genetic and cytogenetic alterations that initiate and drive the development of MPNs have largely been defined, and we summarize these here.
RECENT FINDINGS:
In recent years, advances in understanding the pathogenesis of MPNs have defined a long-preclinical phase in JAK2-mutant MPN, identified genetic loci associated with MPN predisposition and uncovered mechanistic insights in CALR-mutant MPN. The integration of molecular genetics into prognostic risk models is well-established in myelofibrosis and ongoing studies are interrogating the prognostic implications of concomitant mutations in ET and PV. Despite all these advances, the field is deficient in clonally selective therapies to effectively target the MPN clone at any stage of disease, from pre-clinical to advanced. Although the biological understanding of the pathogenesis of MPNs has progressed quickly, substantial knowledge gaps remain, including in the molecular mechanisms underlying MPN progression and myelofibrotic transformation. An ongoing goal for the MPN field is to translate advances in biological understanding to improved treatments for patients.
AuthorsBenjamin Rolles, Ann Mullally
JournalCurrent hematologic malignancy reports (Curr Hematol Malig Rep) Vol. 17 Issue 6 Pg. 319-329 (12 2022) ISSN: 1558-822X [Electronic] United States
PMID36336766 (Publication Type: Journal Article, Review, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Chemical References
  • Janus Kinase 2
Topics
  • Humans
  • Myeloproliferative Disorders (genetics, pathology)
  • Janus Kinase 2 (genetics)
  • Primary Myelofibrosis (genetics)
  • Mutation
  • Hematologic Neoplasms (genetics)
  • Prognosis

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