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.

  • Review
  • Published:

Oncogenic re-wiring of cellular signaling pathways

Abstract

Signaling pathways in mammalian cells are assembled and regulated by a finely controlled network of protein–protein and protein–phospholipid interactions, mediated by dedicated signaling domains and their cognate binding motifs. The domain-based modular architecture of signaling proteins may have facilitated the evolution of complex biological systems, and can be exploited experimentally to generate synthetic signaling pathways and artificial mechanisms of autoregulation. Pathogenic proteins, such as those encoded by bacteria and viruses, frequently form ectopic signaling complexes to respecify cellular behavior. In a similar fashion, proteins expressed as a consequence of oncogenic fusions, mutations or amplifications can elicit ectopic protein–protein interactions that re-wire signaling pathways, in a fashion that promotes malignancy. Compounds that directly or indirectly reverse these aberrant interactions offer new possibilities for therapy in cancer.

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
Figure 2
Figure 3
Figure 4

Similar content being viewed by others

References

  • Aghazadeh B, Lowry WE, Huang XY, Rosen MK . (2000). Structural basis for relief of autoinhibition of the Dbl homology domain of proto-oncogene Vav by tyrosine phosphorylation. Cell 102: 624–633.

    Article  Google Scholar 

  • Anderson D, Koch CA, Grey L, Ellis C, Moran MF, Pawson T . (1990). Binding of SH2 domains of phospholipase Cγ1, GAP, and Src to activated growth factor receptors. Science 250: 979–982.

    Article  CAS  Google Scholar 

  • Bhattacharyya RP, Remenyi A, Yeh BJ, Lim WA . (2006). Domains, motifs, and scaffolds: the role of modular interactions in the evolution and wiring of cell signaling circuits. Annu Rev Biochem 75: 655–680.

    Article  CAS  Google Scholar 

  • Bilder D . (2004). Epithelial polarity and proliferation control: links from the Drosophila neoplastic tumor suppressors. Genes Dev 18: 1909–1925.

    Article  CAS  Google Scholar 

  • Brown MT, Cooper JA . (1996). Regulation, substrates and functions of Src. Biochem Biophys Acta 1287: 121–149.

    PubMed  Google Scholar 

  • Brunet A, Bonni A, Zigmond MJ, Lin MZ, Juo P, Hu LS et al. (1999). Akt promotes cell survival by phosphoylating and inhibiting a forkhead transcription factor. Cell 96: 857–868.

    Article  CAS  Google Scholar 

  • Bustelo XR . (2000). Regulatory and signaling properties of the Vav family. Mol Cell Biol 20: 1461–1477.

    Article  CAS  Google Scholar 

  • Dueber JE, Yeh BJ, Chak K, Lim WA . (2003). Reprogramming control of an allosteric signaling switch through modular recombination. Science 301: 1904–1908.

    Article  CAS  Google Scholar 

  • Engelman JA, Luo J, Cantley LC . (2006). The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Nat Rev Genet 7: 606–619.

    Article  CAS  Google Scholar 

  • Frischknecht F, Moreau V, Rottger S, Gonfloni S, Reckmann I, Superti-Furga G et al. (1999). Actin-based motility of vaccinia virus mimics receptor tyrosine kinase signalling. Nature 401: 926–929.

    Article  CAS  Google Scholar 

  • Gruenheid S, DeVinney R, Bladt F, Goosney D, Gelkop S, Gish GD et al. (2001). Enteropathogenic E. coli Tir binds Nck to initiate actin pedestal formation in host cells. Nat Cell Biol 3: 856–859.

    Article  CAS  Google Scholar 

  • Haglund K, Dikic I . (2005). Ubiquitylation and cell signaling. EMBO J 24: 3353–3359.

    Article  CAS  Google Scholar 

  • He Y, Wertheim JA, Xu L, Miller JP, Karnell FG, Choi JK et al. (2002). The coiled-coil domain and Tyr177 of bcr are required to induce a murine chronic myelogenous leukemia-like disease by bcr/abl. Blood 99: 2957–2968.

    Article  CAS  Google Scholar 

  • Heldin CH . (1995). Dimerization of cell surface receptors in signal transduction. Cell 80: 213–223.

    Article  CAS  Google Scholar 

  • Howard PL, Chia MC, Del Rizzo S, Liu F-F, Pawson T . (2003). Re-directing tyrosine kinase signaling to an apoptotic caspase pathway through chimeric adaptor proteins. Proc Natl Acad Sci USA 100: 11267–11272.

    Article  CAS  Google Scholar 

  • Hu J, Liu J, Ghirlando R, Saltiel AR, Hubbard SR . (2003). Structural basis for recruitment of the adaptor protein APS to the activated insulin receptor. Mol Cell 12: 1379–1389.

    Article  CAS  Google Scholar 

  • Hubbard SR . (1997). Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analog. EMBO J 16: 5572–5581.

    Article  CAS  Google Scholar 

  • Hubbard SR, Till JH . (2000). Protein tyrosine kinase structure and function. Annu Rev Biochem 69: 373–398.

    Article  CAS  Google Scholar 

  • Hunter T . (2000). Signaling – 2000 and beyond. Cell 100: 113–127.

    Article  CAS  Google Scholar 

  • Jones RB, Gordus A, Krall JA, Macbeath G . (2006). A quantitative protein interaction network for the ErbB receptors using protein microarrays. Nature 439: 168–174.

    Article  CAS  Google Scholar 

  • Kim AS, Kakalis LT, Abdul-Manan N, Liu GA, Rosen MK . (2000). Autoinhibition and activation mechanisms of the Wiskott–Aldrich syndrome protein. Nature 404: 151–158.

    Article  CAS  Google Scholar 

  • Kim JH, Chu SC, Gramlich JL, Pride YB, Babendreier E, Chauhan D et al. (2005). Activation of the PI3K/mTOR pathway by BCR–ABL contributes to increased production of reactive oxygen species. Blood 105: 1717–1723.

    Article  CAS  Google Scholar 

  • Kong-Beltran M, Seshagiri S, Zha J, Zhu W, Bhawe K, Mendoza N et al. (2006). Somatic mutations lead to an oncogenic deletion of met in lung cancer. Cancer Res 66: 283–289.

    Article  CAS  Google Scholar 

  • Liu BA, Jabonowski K, Raina M, Arce M, Pawson T, Nash PD . (2006). The human and mouse complement of SH2 domain proteins – establishing the boundaries of phosphotyrosine signaling. Mol Cell 22: 851–868.

    Article  Google Scholar 

  • Llorca O, Arias-Palomo E, Zugaza L, Bustelo XR . (2005). Global conformational rearrangements during the activation of the GDP/GTP exchange factor Vav3. EMBO J 24: 1330–1340.

    Article  CAS  Google Scholar 

  • Macara IG . (2004). Parsing the polarity code. Nat Rev Mol Cell Biol 5: 220–231.

    Article  CAS  Google Scholar 

  • McWhirter JR, Galasso DL, Wang JY . (1993). A coiled-coil oligomerization domain of Bcr is essential for the transforming function of Bcr–Abl oncoproteins. Mol Cell Biol 13: 7587–7595.

    Article  CAS  Google Scholar 

  • Million RP, Van Etten RA . (2000). The Grb2 binding site is required for the induction of chronic myeloid leukemia-like disease in mice by the Bcr/Abl tyrosine kinase. Blood 96: 664–670.

    CAS  Google Scholar 

  • Minucci S, Nervi C, Lo Coco F, Pelicci PG . (2001). Histone deacetylases: a common molecular target for differentiation treatment of acute myeloid leukemias. Oncogene 20: 3110–3115.

    Article  CAS  Google Scholar 

  • Nagar B, Hantschel O, Young MA, Scheffzek K, Veach D, Bornmann W et al. (2003). Structural basis for the autoinhibition of c-Abl tyrosine kinase. Cell 112: 859–872.

    Article  CAS  Google Scholar 

  • Pawson T, Nash P . (2000). Protein–protein interactions define specificity in signal transduction. Genes Dev 14: 1027–1047.

    CAS  PubMed  Google Scholar 

  • Pawson T, Nash P . (2003). Assembly of cell regulatory systems through protein interaction domains. Science 300: 445–452.

    Article  CAS  Google Scholar 

  • Pendergast AM, Quilliam LA, Cripe LD, Bassing CH, Dai Z, Li N et al. (1993). BCR–ABL-induced oncogenesis is mediated by direct interaction with the SH2 domain of the GRB-2 adaptor protein. Cell 75: 175–185.

    Article  CAS  Google Scholar 

  • Puil L, Liu X, Gish G, Mbamalu G, Bowtell D, Pelicci PG et al. (1994). BCR–ABL oncoproteins bind directly to activators of the ras signalling pathway. EMBO J 13: 764–773.

    Article  CAS  Google Scholar 

  • Rowley JD . (1990). The Philadelphia chromosome translocation. A paradigm for understanding leukemia. Cancer 65: 2178–2184.

    Article  CAS  Google Scholar 

  • Sattler M, Mohi MG, Pride YB, Quinnan LR, Malouf NA, Podar K et al. (2002). Critical role for Gab2 in transformation by BCR/ABL. Cancer Cell 1: 479–492.

    Article  CAS  Google Scholar 

  • Sicheri F, Moarefi I, Kuriyan J . (1997). Crystal structure of the Src family tyrosine kinase Hck. Nature 385: 602–609.

    Article  CAS  Google Scholar 

  • Thomas M, Massimi P, Navarro C, Borg JP, Banks L . (2005). The hScrib/Dig apico-basal control complex is differentially targeted by HPV-16 and HPV-18 E6 proteins. Oncogene 24: 6222–6230.

    Article  CAS  Google Scholar 

  • Weinmaster G, Zoller MJ, Smith M, Hinze E, Pawson T . (1984). Mutagenesis of Fujinami sarcoma virus: evidence that tyrosine phosphorylation of P130gap-fps modulates its biological activity. Cell 37: 559–568.

    Article  CAS  Google Scholar 

  • Xu W, Harrison SC, Eck MJ . (1997). Three-dimensional structure of the tyrosine kinase c-Src. Nature 385: 595–602.

    Article  CAS  Google Scholar 

  • Zarrinpar A, Bhattacharyya RP, Lim WA . (2003). The structure and function of proline recognition domains. Sci STKE, 2003. RE8.

  • Zha J, Harada H, Yang E, Jockel J, Korsmeyer SJ . (1996). Serine phosphorylation of death agonist BAD in response to survival factor results in binding to 14-3-3 not BCL-XL . Cell 87: 619–628.

    Article  CAS  Google Scholar 

  • Zhou J, Peres L, Honore N, Nasr R, Zhu J, de The H . (2006). Dimerization-induced corepressor binding and relaxed DNA-binding specificity are critical for PML/RARA-induced immortalization. Proc Natl Acad Sci USA 103: 9238–9243.

    Article  CAS  Google Scholar 

  • Zhu J, Zhou J, Peres L, Riaucoux F, Honore N, Kogan S et al. (2005). A sumoylation site in PML. RARA is essential for leukemic transformation. Cancer Cell 7: 143–153.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Work in the authors' laboratory is supported by grants from the Canadian Institutes for Health Research, the National Cancer Institute of Canada, and Genome Canada through the Ontario Genomics Institute. TP is a Distinguished Investigator of the CIHR.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to T Pawson.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pawson, T., Warner, N. Oncogenic re-wiring of cellular signaling pathways. Oncogene 26, 1268–1275 (2007). https://doi.org/10.1038/sj.onc.1210255

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.onc.1210255

Keywords

This article is cited by

Search

Quick links