International Journal of Hematology

, Volume 91, Issue 2, pp 189–200

The current status and the future of JAK2 inhibitors for the treatment of myeloproliferative diseases


    • Rigel Pharmaceuticals Inc.
  • Nan Lin
    • Rigel Pharmaceuticals Inc.
  • Donald G. Payan
    • Rigel Pharmaceuticals Inc.
  • Vadim Markovtsov
    • Rigel Pharmaceuticals Inc.
Progress in Hematology Molecular mechanism, diagnosis, and treatment for myeloproliferative neoplasms

DOI: 10.1007/s12185-010-0531-y

Cite this article as:
Hitoshi, Y., Lin, N., Payan, D.G. et al. Int J Hematol (2010) 91: 189. doi:10.1007/s12185-010-0531-y


Janus kinases (JAKs) are critical components of cytokine signaling pathways which regulate immunity, inflammation, hematopoiesis, growth, and development. The recent discovery of JAK2-activating mutations as a causal event in the majority of patients with Philadelphia chromosome negative (Ph−) myeloproliferative disorders (MPDs) prompted many pharmaceutical companies to develop JAK2-selective inhibitors for the treatment of MPDs. JAK2 inhibitors effectively reduce JAK2-driven phosphorylation of signal transducer and activator of transcription 5, and cell proliferation and cell survival in JAK2-activated cells in vitro and in vivo. Most inhibitors are currently being evaluated in patients with one form of MPD, myelofibrosis. Patients treated with these inhibitors experienced a rapid reduction of splenomegaly, significant improvement of constitutional symptoms, and increased daily activity with few adverse events. A partial reduction of JAK2V617F disease burden during the treatment with JAK2 inhibitors was also observed. The inhibitors appear to have a therapeutic benefit in the treatment of these disorders. The results of ongoing clinical trials will allow further evaluation of clinical benefits and safety of these compounds. In this review, the authors summarize the status of JAK2 inhibitors in development and discuss their benefits and challenges.


JAK2 kinase inhibitorMyeloproliferative disordersJAK2V617F

Copyright information

© The Japanese Society of Hematology 2010