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.

  • Brief Communication
  • Published:

RNF43 is frequently mutated in colorectal and endometrial cancers

Abstract

We report somatic mutations of RNF43 in over 18% of colorectal adenocarcinomas and endometrial carcinomas. RNF43 encodes an E3 ubiquitin ligase that negatively regulates Wnt signaling. Truncating mutations of RNF43 are more prevalent in microsatellite-unstable tumors and show mutual exclusivity with inactivating APC mutations in colorectal adenocarcinomas. These results indicate that RNF43 is one of the most commonly mutated genes in colorectal and endometrial cancers.

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

Access options

Buy this article

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

Figure 1: RNF43 mutations in colorectal and endometrial cancers.
Figure 2: Association of RNF43 mutations with MSI status and APC mutations.

Similar content being viewed by others

References

  1. Koo, B.K. et al. Nature 488, 665–669 (2012).

    Article  CAS  Google Scholar 

  2. Jiang, X. et al. Proc. Natl. Acad. Sci. USA 110, 12649–12654 (2013).

    Article  CAS  Google Scholar 

  3. Wu, J. et al. Proc. Natl. Acad. Sci. USA 108, 21188–21193 (2011).

    Article  CAS  Google Scholar 

  4. Jiao, Y. et al. J. Pathol. 232, 428–435 (2014).

    Article  CAS  Google Scholar 

  5. Hodis, E. et al. Cell 150, 251–263 (2012).

    Article  CAS  Google Scholar 

  6. Cancer Genome Atlas Network. Nature 490, 61–70 (2012).

  7. Stransky, N. et al. Science 333, 1157–1160 (2011).

    Article  CAS  Google Scholar 

  8. Clevers, H. & Nusse, R. Cell 149, 1192–1205 (2012).

    Article  CAS  Google Scholar 

  9. Cancer Genome Atlas Network. Nature 487, 330–337 (2012).

  10. Seshagiri, S. et al. Nature 488, 660–664 (2012).

    Article  CAS  Google Scholar 

  11. Liao, X. et al. N. Engl. J. Med. 367, 1596–1606 (2012).

    Article  CAS  Google Scholar 

  12. Cancer Genome Atlas Research Network. Nature 497, 67–73 (2013).

  13. Wang, K. et al. Nat. Genet. 43, 1219–1223 (2011).

    Article  CAS  Google Scholar 

  14. Zang, Z.J. et al. Nat. Genet. 44, 570–574 (2012).

    Article  CAS  Google Scholar 

  15. Wang, K. et al. Nat. Genet. 46, 573–582 (2014).

    Article  CAS  Google Scholar 

  16. Cancer Genome Atlas Research Network. Nature 513, 202–209 (2014).

  17. Van Allen, E.M. et al. Nat. Med. 20, 682–688 (2014).

    Article  CAS  Google Scholar 

  18. Cibulskis, K. et al. Nat. Biotechnol. 31, 213–219 (2013).

    Article  CAS  Google Scholar 

  19. Robinson, J.T. et al. Nat. Biotechnol. 29, 24–26 (2011).

    Article  CAS  Google Scholar 

  20. Kim, D. & Salzberg, S.L. Genome Biol. 12, R72 (2011).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank S. Bahl, E. Nickerson and S. Chauvin for project management and A. Regev for help with computing resources, as well as A. Sivachenko, F. Huang and P. Tamayo for helpful discussions. This work was supported by the Dana-Farber Cancer Institute Leadership Council, the 2014 Colon Cancer Alliance–American Association for Cancer Research Fellowship for Biomarker Research, grant 14-40-40-GIAN, the Perry S. Levy Endowed Fellowship (M.G.), award T32GM007753 from the National Institute of General Medical Sciences, the Herchel Smith Fellowship (E.H.) and the Agrusa Fund for Colorectal Cancer Research (C.S.F.), as well as National Human Genome Research Institute grant U54HG003067 (E.S.L. and S.B.G.) and National Cancer Institute grants, K07CA190673 (R.N.), P01CA87969, UM1CA167552 and R01CA151993 (S.O.), R01CA118553 and R01CA168141 (C.S.F.) and P50CA127003 (M.G., W.C.H., L.A.G. and C.S.F.).

Author information

Authors and Affiliations

Authors

Contributions

M.G., E.H., W.C.H., G.G., S.B.G., E.S.L., S.O., C.S.F. and L.A.G. designed research. M.G., E.H., X.J.M., M.Y., J.R., K.C., G.S., M.S.L., Z.R.Q., R.N. and E.M.V.A. performed research. G.G., S.B.G., E.S.L., S.O. and C.S.F. contributed new reagents and analytic tools. M.G., E.H., X.J.M., E.M.V.A. and L.A.G. analyzed data. M.G., E.H. and L.A.G. wrote the manuscript.

Corresponding author

Correspondence to Levi A Garraway.

Ethics declarations

Competing interests

L.A.G. is a consultant for an equity holder in Foundation Medicine. L.A.G. is also a consultant to Novartis, Millenium/Takeda and Boehringer Ingelheim and is a recipient of a grant from Novartis.

Integrated supplementary information

Supplementary Figure 1 Manual review of RNF43 p.Gly659fs mutations using Integrated Genomics Viewer and validation by Sanger sequencing.

Representative Integrated Genomics Viewer screenshots and Sanger sequencing chromatograms for RNF43 p.Gly659fs-mutated tumor (a,c) and matched normal (b,d) tissue.

Supplementary information

Supplementary Text and Figures

Manual review of RNF43 G659fs mutations using Integrated Genomics Viewer and validation by Sanger sequencing. (PDF 262 kb)

Supplementary Tables 1–10

Supplementary Tables 1–10 (XLSX 35911 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Giannakis, M., Hodis, E., Jasmine Mu, X. et al. RNF43 is frequently mutated in colorectal and endometrial cancers. Nat Genet 46, 1264–1266 (2014). https://doi.org/10.1038/ng.3127

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/ng.3127

This article is cited by

Search

Quick links

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter — top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research