Skip to main content
Log in

BCR-ABL signaling

A new STATus in CML

  • News & Views
  • Published:

From Nature Chemical Biology

View current issue Submit your manuscript

A combination of genetic and pharmacological approaches using mouse leukemia models show that STAT5 phosphorylation is one of the major drivers of the proliferation of Philadelphia chromosome–positive (BCR-ABL-positive or Ph+) chronic myeloid leukemia. Once BCR-ABL expression has been established, JAK2 is required only for lymphoid cell transformation, not for the maintenance of the lymphoid or myeloid leukemia.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1: Schematic representation of STAT5 activation in normal hematopoietic stem cell and in Ph+ CML.

Katie Vicari

References

  1. Melo, J.V. & Barnes, D.J. Nat. Rev. Cancer 7, 441–453 (2007).

    Article  CAS  PubMed  Google Scholar 

  2. Clark, S.S. et al. Science 235, 85–88 (1987).

    Article  CAS  PubMed  Google Scholar 

  3. Quintas-Cardáma, A., Kantarjian, H. & Cortes, J. Nat. Rev. Drug Discov. 6, 834–848 (2007).

    Article  PubMed  Google Scholar 

  4. Druker, B.J. et al. N. Engl. J. Med. 355, 2408–2417 (2006).

    Article  CAS  PubMed  Google Scholar 

  5. Padmanabhan, S. et al. Future Oncol. 4, 359–377 (2008).

    Article  CAS  PubMed  Google Scholar 

  6. Fabbro, D., et al. Biochim. Biophys. Acta. 1804, 454–462 (2010).

    Article  CAS  PubMed  Google Scholar 

  7. O'Hare, T. et al. Cancer Cell 16, 401–412 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Carlesso, N., Frank, D.A. & Griffin, J.D. J. Exp. Med. 183, 811–820 (1996).

    Article  CAS  PubMed  Google Scholar 

  9. Sillaber, C. et al. Blood 95, 2118–2125 (2000).

    CAS  PubMed  Google Scholar 

  10. Hantschel, O. et al. Nat. Chem. Biol. 8, 285–293 (2012).

    Article  CAS  PubMed  Google Scholar 

  11. Melnick, J.S. et al. Proc. Natl. Acad. Sci. USA 103, 3153–3158 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Warsch, W. et al. Blood 117, 3409–3420 (2011).

    Article  CAS  PubMed  Google Scholar 

  13. Nelson, E.A. et al. Blood 117, 3421–3429 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Doriano Fabbro.

Ethics declarations

Competing interests

The author declares no competing financial interests.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fabbro, D. A new STATus in CML. Nat Chem Biol 8, 228–229 (2012). https://doi.org/10.1038/nchembio.900

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nchembio.900

  • Springer Nature America, Inc.

This article is cited by

Navigation