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.

  • Technical Report
  • Published:

Invasive three-dimensional organotypic neoplasia from multiple normal human epithelia

Abstract

Refined cancer models are required if researchers are to assess the burgeoning number of potential targets for cancer therapeutics in a clinically relevant context that allows a fast turnaround. Here we use tumor-associated genetic pathways to transform primary human epithelial cells from the epidermis, oropharynx, esophagus and cervix into genetically defined tumors in a human three-dimensional (3D) tissue environment that incorporates cell-populated stroma and intact basement membrane. These engineered organotypic tissues recapitulated natural features of tumor progression, including epithelial invasion through basement membrane, a complex process that is necessary for biological malignancy in 90% of human cancers. Invasion was rapid and was potentiated by stromal cells. Oncogenic signals in 3D tissue, but not 2D culture, resembled gene expression profiles from spontaneous human cancers. We screened 3D organotypic neoplasia with well-characterized signaling pathway inhibitors to distill a clinically faithful cancer gene signature. Multitissue 3D human tissue cancer models may provide an efficient and relevant complement to current approaches to characterizing cancer progression.

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: 3D organotypic human epithelial tissue.
Figure 2: Organotypic neoplasia from multiple stratified epithelia.
Figure 3: Stromal cells potentiate invasion in organotypic neoplasia.
Figure 4: Analysis of organotypic neoplasia.

Similar content being viewed by others

Accession codes

Accessions

Gene Expression Omnibus

References

  1. Stratton, M.R., Campbell, P.J. & Futreal, P.A. The cancer genome. Nature 458, 719–724 (2009).

    Article  CAS  Google Scholar 

  2. Campbell, P.J. et al. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat. Genet. 40, 722–729 (2008).

    Article  CAS  Google Scholar 

  3. Chin, L. & Gray, J.W. Translating insights from the cancer genome into clinical practice. Nature 452, 553–563 (2008).

    Article  CAS  Google Scholar 

  4. Rangarajan, A., Hong, S.J., Gifford, A. & Weinberg, R.A. Species- and cell type-specific requirements for cellular transformation. Cancer Cell 6, 171–183 (2004).

    Article  CAS  Google Scholar 

  5. Hamad, N.M. et al. Distinct requirements for Ras oncogenesis in human versus mouse cells. Genes Dev. 16, 2045–2057 (2002).

    Article  CAS  Google Scholar 

  6. Hahn, W.C. et al. Creation of human tumour cells with defined genetic elements. Nature 400, 464–468 (1999).

    Article  CAS  Google Scholar 

  7. Elenbaas, B. et al. Human breast cancer cells generated by oncogenic transformation of primary mammary epithelial cells. Genes Dev. 15, 50–65 (2001).

    Article  CAS  Google Scholar 

  8. Lundberg, A.S. et al. Immortalization and transformation of primary human airway epithelial cells by gene transfer. Oncogene 21, 4577–4586 (2002).

    Article  CAS  Google Scholar 

  9. Dajee, M. et al. NF-kappaB blockade and oncogenic Ras trigger invasive human epidermal neoplasia. Nature 421, 639–643 (2003).

    Article  CAS  Google Scholar 

  10. Lazarov, M. et al. Cdk4 coexpression with Ras generates malignant human epidermal tumorigenesis. Nat. Med. 8, 1105–1114 (2002).

    Article  CAS  Google Scholar 

  11. Horner, M.J. et al. SEER Cancer Statistics Review, 1975–2006 <http://seer.cancer.gov/csr/1975_2007/> (National Cancer Institute, Bethesda, Maryland, 2010).

  12. Egeblad, M., Littlepage, L.E. & Werb, Z. The fibroblastic coconspirator in cancer progression. Cold Spring Harb. Symp. Quant. Biol. 70, 383–388 (2005).

    Article  CAS  Google Scholar 

  13. Hu, M. et al. Regulation of in situ to invasive breast carcinoma transition. Cancer Cell 13, 394–406 (2008).

    Article  CAS  Google Scholar 

  14. Marx, J. Cancer biology. All in the stroma: cancer's Cosa Nostra. Science 320, 38–41 (2008).

    Article  CAS  Google Scholar 

  15. Bissell, M.J., Kenny, P.A. & Radisky, D.C. Microenvironmental regulators of tissue structure and function also regulate tumor induction and progression: the role of extracellular matrix and its degrading enzymes. Cold Spring Harb. Symp. Quant. Biol. 70, 343–356 (2005).

    Article  CAS  Google Scholar 

  16. Khavari, P.A. Modelling cancer in human skin tissue. Nat. Rev. Cancer 6, 270–280 (2006).

    Article  CAS  Google Scholar 

  17. Tarutani, M., Cai, T., Dajee, M. & Khavari, P.A. Inducible activation of Ras and Raf in adult epidermis. Cancer Res. 63, 319–323 (2003).

    CAS  PubMed  Google Scholar 

  18. Marinkovich, M.P., Keene, D.R., Rimberg, C.S. & Burgeson, R.E. Cellular origin of the dermal-epidermal basement membrane. Dev. Dyn. 197, 255–267 (1993).

    Article  CAS  Google Scholar 

  19. Kao, W.T. et al. Investigation of MMP-2 and -9 in a highly invasive A431 tumor cell sub-line selected from a Boyden chamber assay. Anticancer Res. 28, 2109–2120 (2008).

    CAS  PubMed  Google Scholar 

  20. Toruner, G.A. et al. Association between gene expression profile and tumor invasion in oral squamous cell carcinoma. Cancer Genet. Cytogenet. 154, 27–35 (2004).

    Article  CAS  Google Scholar 

  21. Kuriakose, M.A. et al. Selection and validation of differentially expressed genes in head and neck cancer. Cell. Mol. Life Sci. 61, 1372–1383 (2004).

    Article  CAS  Google Scholar 

  22. Reuter, J.A. et al. Modeling inducible human tissue neoplasia identifies an extracellular matrix interaction network involved in cancer progression. Cancer Cell 15, 477–488 (2009).

    Article  CAS  Google Scholar 

  23. Lee, T.L. et al. A novel nuclear factor-kappaB gene signature is differentially expressed in head and neck squamous cell carcinomas in association with TP53 status. Clin. Cancer Res. 13, 5680–5691 (2007).

    Article  CAS  Google Scholar 

  24. Forbes, S.A. et al. The catalogue of somatic mutations in cancer (COSMIC). Curr. Protoc. Hum. Genet. 57, 10.11.1–10.11.26 (2008).

    Google Scholar 

  25. Cancer Genome Atlas Research Network. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 455, 1061–1068 (2008).

  26. Luo, J., Solimini, N.L. & Elledge, S.J. Principles of cancer therapy: oncogene and non-oncogene addiction. Cell 136, 823–837 (2009).

    Article  CAS  Google Scholar 

  27. Petersen, O.W., Ronnov-Jessen, L., Howlett, A.R. & Bissell, M.J. Interaction with basement membrane serves to rapidly distinguish growth and differentiation pattern of normal and malignant human breast epithelial cells. Proc. Natl. Acad. Sci. USA 89, 9064–9068 (1992).

    Article  CAS  Google Scholar 

  28. Cox, A.D. & Der, C.J. The raf inhibitor paradox: unexpected consequences of targeted drugs. Cancer Cell 17, 221–223 (2010).

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by National Institutes of Health grant AR43799 to P.A.K. We thank A. Oro, P. Marinkovich, H. Chang, D. Felsher, S. Artandi, A. Sweet-Cordero, M. Scott, G. Sen, Z. Siprashvili, M. Kretz and J. Reuter for presubmission review of the manuscript. T.W.R. is the recipient of career development award National Institutes of Health K08AR053195.

Author information

Authors and Affiliations

Authors

Contributions

T.W.R. designed the experiments, performed research, interpreted data and wrote the manuscript. J.M.C. performed experiments. D.J.W. helped to analyze expression array data. P.A.K. helped design and interpret experiments and helped write the manuscript.

Corresponding author

Correspondence to Paul A Khavari.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary Text and Figures

Supplementary Figures 1–8, Supplementary Tables 1–5 and Supplementary Methods (PDF 2632 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ridky, T., Chow, J., Wong, D. et al. Invasive three-dimensional organotypic neoplasia from multiple normal human epithelia. Nat Med 16, 1450–1455 (2010). https://doi.org/10.1038/nm.2265

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nm.2265

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