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  • Acquired Diseases
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Inhibition of human lung carcinoma cell growth by apoptosis induction using Semliki Forest virus recombinant particles

Abstract

We have utilised cell cultures and growth of tumours in nude mice to assess further the potential of the Semliki Forest virus (SFV) vector as a cancer therapy agent. This vector is a transient RNA-based expression vector, and we have previously shown that SFV and its derived vector can induce p53-independent apoptosis by expression of the nonstructural region of the virus genome. Apoptosis induction is therefore an inherent property of the vector and is not dependent on heterologous gene expression. SFV recombinant suicide particles (rSFV) were shown to induce apoptosis in H358a cells, which are human non-small cell lung carcinoma cells deleted in p53. EGFP-expressing rSFV also inhibited the growth of developing H358a spheroids. Direct injection of rSFV into H358a tumours subcutaneously implanted as xenografts in nu/nu mice inhibited tumour growth, and in some cases caused complete regression. It is concluded that tumour growth suppression induced by rSFV was due to apoptosis induction and that the vector has an inherent cell death-promoting and antitumour activity. These results, as well as previous work by other authors on targeting and immune stimulation using alphavirus vectors, indicate that SFV recombinant particles in particular have considerable potential for further exploitation as a cancer therapy agent.

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References

  1. Swisher SG et al. Adenovirus-mediated p53 gene transfer in advanced non-small-cell lung cancer J Natl Cancer Inst 1999 91: 763–771

    Article  CAS  PubMed  Google Scholar 

  2. Roth JA et al. Retrovirus-mediated wild-type p53 gene transfer to tumors of patients with lung cancer Nature Med 1996 2: 985–991

    Article  CAS  PubMed  Google Scholar 

  3. Quazilbash MH et al. Cancer gene therapy using a novel adeno-associated virus vector expressing human wild-type p53 Gene Therapy 1997 4: 675–682

    Article  Google Scholar 

  4. Takahashi T et al. p53: A frequent target for genetic abnormalities in lung cancer Science 1989 246: 491–494

    Article  CAS  PubMed  Google Scholar 

  5. Berglund P et al. Semliki Forest virus expression system: production of conditionally infectious recombinant particles Bio/Technology 1993 11: 916–920

    CAS  Google Scholar 

  6. Smerdou C, Liljeström P . Two-helper RNA system for production of recombinant Semliki Forest virus particles J Virol 1999 73: 1092–1098

    CAS  PubMed  PubMed Central  Google Scholar 

  7. Atkins GJ, Sheahan BJ, Liljeström P . The molecular pathogenesis of Semliki Forest virus: a model virus made useful? J Gen Virol 1999 80: 2287–2297

    Article  CAS  PubMed  Google Scholar 

  8. Berglund P et al. Immunization with recombinant Semliki Forest virus induces protection against influenza challenge in mice Vaccine 1999 17: 497–507

    Article  CAS  PubMed  Google Scholar 

  9. Fleeton MN et al. Recombinant Semliki Forest virus particles expressing louping ill virus antigens induce a better protective response than plasmid-based DNA vaccines or an inactivated whole particle vaccine J Gen Virol 2000 81: 749–758

    Article  CAS  PubMed  Google Scholar 

  10. Glasgow GM et al. Death mechanisms in cultured cells infected by Semliki Forest virus J Gen Virol 1997 78: 1559–1563

    Article  CAS  PubMed  Google Scholar 

  11. Glasgow GM et al. The Semliki Forest virus vector induces p53-independent apoptosis J Gen Virol 1998 79: 2405–2410

    Article  CAS  PubMed  Google Scholar 

  12. Sutherland RM . Cell and environment interactions in tumor microregions: the multicell spheroid model Science 1988 240: 177–184

    Article  CAS  PubMed  Google Scholar 

  13. Asselin-Paturel C et al. Transfer of the murine interleukin-12 gene in vivo by a Semliki Forest virus vector induces B16 tumor regression through inhibition of tumor blood vessel formation monitored by Doppler ultrasonography Gene Therapy 1998 5: 606–615

    Google Scholar 

  14. Fujiwara T et al. Induction of chemosensitivity in human lung cancer cells in vivo by adenovirus-mediated transfer of the wild-type p53 gene Cancer Res 1994 54: 2287–2291

    CAS  PubMed  Google Scholar 

  15. Fujiwara T et al. Therapeutic effect of a retroviral wild-type p53 expression vector in an orthotopic lung cancer model J Natl Cancer Inst 1994 86: 1458–1462

    Article  CAS  PubMed  Google Scholar 

  16. Majno G, Joris I . Apoptosis, oncosis, and necrosis. An overview of cell death Am J Pathol 1995 146: 3–15

    CAS  PubMed  PubMed Central  Google Scholar 

  17. Donnelly JJ et al. DNA vaccines Ann Rev Immunol 1997 15: 617–626

    Article  CAS  Google Scholar 

  18. Ying H et al. Cancer therapy using a self-replicating RNA vaccine Nature Med 1999 5: 823–827

    Article  CAS  PubMed  Google Scholar 

  19. Colmenero P et al. Induction of P815 tumor immunity by recombinant Semliki Forest virus expressing the P1A gene Gene Therapy 1999 6: 1728–1733

    Article  CAS  PubMed  Google Scholar 

  20. Ohno K et al. Cell-specific targeting of Sindbis virus vectors displaying IgG-binding domains of Protein A Nat Biotechnol 1997 15: 763–767

    Article  CAS  PubMed  Google Scholar 

  21. Skehan P et al. New colorimetric cytotoxicity assay for anticancer-drug screening J Natl Cancer Inst 1990 82: 1107–1112

    Article  CAS  PubMed  Google Scholar 

  22. Korff T, Augustin HG . Integration of endothelial cells in multicellular spheroids prevents apoptosis and induces differentiation J Cell Biol 1998 143: 1341–1352

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank Dr Marina Fleeton and Professor Peter Liljeström for providing the vectors used in this study and for help with the vector system, and Ms Marie Moore for her assistance with pathological studies. We are also grateful to Ms Deborah Mansfield and Dr Jack Roth for providing the H358a cells. This work was supported by the Cancer Research Advancement Board of the Irish Cancer Society, the Irish Health Research Board, BioResearch Ireland, the Wellcome Trust and the European Union Biotechnology Programme.

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Murphy, AM., Morris-Downes, M., Sheahan, B. et al. Inhibition of human lung carcinoma cell growth by apoptosis induction using Semliki Forest virus recombinant particles. Gene Ther 7, 1477–1482 (2000). https://doi.org/10.1038/sj.gt.3301263

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