4.7 Article

The polycythemia vera-associated Jak2 V617F mutant induces tumorigenesis in nude mice

期刊

INTERNATIONAL IMMUNOPHARMACOLOGY
卷 9, 期 7-8, 页码 870-877

出版社

ELSEVIER
DOI: 10.1016/j.intimp.2009.03.011

关键词

Jak2; Polycythemia vera (PV); V617F; Anti-apoptosis; Tumorigenesis

资金

  1. MEXT [19790071]
  2. Research Foundation for Pharmaceutical Sciences
  3. Hi-Tech Research Center Project for Private Universities in Japan
  4. Grants-in-Aid for Scientific Research [19790071] Funding Source: KAKEN

向作者/读者索取更多资源

The somatic Jak2 mutation (V617F) was identified in most patients with polycythemia vera (PV). Here, we show that the activating Jak2 V617F mutant completely protected Ba/F3 cells from cytokine withdrawal-induced apoptotic cell death. Interestingly, Ba/F3 cells expressing Jak2 V617F mutant induced rapid tumorigenesis in nude mice, leading to rapid death. Whereas an injection of Ba/F3 cells expressing wild-type Jak2 had no effect, an injection of Ba/F3 cells expressing Jak2 V617F mutant promptly invaded and spread into various distinct organs, such as the liver and spleen. Strikingly, Jak2 inhibitor, AG490 potently inhibited cytokine-independent cell growth induced by the Jak2 V617F mutant. Also, treatment with AG490 effectively delayed Jak2 V617F mutant-induced tumorigenesis in nude mice. Thus, our results both in vitro and in vivo suggest that Jak2 harboring V617F mutation is a potent oncogene able to promote cell transformation and tumorigenesis. (C) 2009 Elsevier B.V. All rights reserved.

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