Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • News & Views
  • Published:

Chipping away at the lung cancer genome

Kinase inhibitors are now standard treatment for patients with lung cancer whose tumors harbor specific mutant kinases. Four recent studies, including three in this issue (pages 375–384), have identified new fusion proteins involving another receptor tyrosine kinase that may potentially be responsive to existing targeted therapies.

This is a preview of subscription content, access via your institution

Relevant articles

Open Access articles citing this article.

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Molecular subsets of lung adenocarcinoma.

References

  1. Jemal, A. et al. CA Cancer J. Clin. 61, 69–90 (2011).

    Article  Google Scholar 

  2. Pao, W. & Girard, N. Lancet Oncol. 12, 175–180 (2011).

    Article  CAS  Google Scholar 

  3. Li, C. et al. PLoS ONE 6, e28204 (2011).

    Article  CAS  Google Scholar 

  4. Pao, W. et al. Proc. Natl. Acad. Sci. USA 101, 13306–13311 (2004).

    Article  CAS  Google Scholar 

  5. Kwak, E.L. et al. N. Engl. J. Med. 363, 1693–1703 (2010).

    Article  CAS  Google Scholar 

  6. Bergethon, K. et al. J. Clin. Oncol. published online, 10.1200/JCO.2011.35.6345 (3 January 2012).

  7. Kohno, T. et al. Nat. Med. 18, 375–377 (2012).

    Article  CAS  Google Scholar 

  8. Lipson, D. et al. Nat. Med. 18, 382–384 (2012).

    Article  CAS  Google Scholar 

  9. Takeuchi, K. et al. Nat. Med. 18, 378–381 (2012).

    Article  CAS  Google Scholar 

  10. Ju, Y.S. et al. Genome Res. published online, 10.1101/gr.133645.111 (22 December 2011).

  11. Takahashi, M., Ritz, J. & Cooper, G.M. Cell 42, 581–588 (1985).

    Article  CAS  Google Scholar 

  12. Phay, J.E. & Shah, M.H. Clin. Cancer Res. 16, 5936–5941 (2010).

    Article  CAS  Google Scholar 

  13. Chmielecki, J. et al. Nucleic Acids Res. 38, 6985–6996 (2010).

    Article  CAS  Google Scholar 

  14. Ciampi, R. & Nikiforov, Y.E. Endocrinology 148, 936–941 (2007).

    Article  CAS  Google Scholar 

  15. Wells, S.A. Jr. et al. J. Clin. Oncol. 28, 767–772 (2010).

    Article  CAS  Google Scholar 

  16. Sablin, E.P. Curr. Opin. Cell Biol. 12, 35–41 (2000).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to William Pao.

Ethics declarations

Competing interests

W.P. is a consultant for MolecularMD, AstraZeneca, Bristol-Myers Squibb, Sequencing Evolution and Clovis Oncology and received research funding from Enzon, Xcovery, AstraZeneca and Symphogen. The rights to EGFR T790M testing were licensed on behalf of W.P. and others by Memorial Sloan-Kettering Cancer Center to MolecularMD.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pao, W., Hutchinson, K. Chipping away at the lung cancer genome. Nat Med 18, 349–351 (2012). https://doi.org/10.1038/nm.2697

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nm.2697

This article is cited by

Search

Quick links

Nature Briefing: Cancer

Sign up for the Nature Briefing: Cancer newsletter — what matters in cancer research, free to your inbox weekly.

Get what matters in cancer research, free to your inbox weekly. Sign up for Nature Briefing: Cancer