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Egal Gorse 2006-2007

Transfection of Recombinant Plasmid DNA From Immunotoxins into Eukaryotic Cells for the Development of an Antibody Targeted Cancer Therapy. Egal Gorse 2006-2007. Goals. To determine if mammalian carrier cells would accept and express immunotoxin DNA.

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Egal Gorse 2006-2007

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  1. Transfection of Recombinant Plasmid DNA From Immunotoxins into Eukaryotic Cells for the Development of an Antibody Targeted Cancer Therapy Egal Gorse 2006-2007

  2. Goals • To determine if mammalian carrier cells would accept and express immunotoxin DNA. • To evaluate which carrier cells most effectively expressed immunotoxin DNA.

  3. Cancer • Cancer is the leading cause of death in the world (7.6 million per year). • There is no effective treatment for cancer. • Chemotherapy is inefficient (resistance and not targeted). • Immunotoxins have shown promise as an effective cancer therapy (Vallera 2005).

  4. How EpCAMKDEL Kills Cells A T B Binding Outside Inside Cytosol Golgi Apparatus Endoplasmic Reticulum

  5. How EpCAMKDEL Kills Cells A T B Outside Inside Transport Vesicle Cytosol Golgi Apparatus Endoplasmic Reticulum

  6. How EpCAMKDEL Kills Cells A T B Outside Inside Transport Vesicle Cytosol Golgi Apparatus Endoplasmic Reticulum

  7. How EpCAMKDEL Kills Cells A T T B Outside Inside Cytosol Transport Vesicle Golgi Apparatus Endoplasmic Reticulum

  8. How EpCAMKDEL Kills Cells T Outside Inside Cytosol A T B Golgi Apparatus Transport Vesicle Endoplasmic Reticulum

  9. How EpCAMKDEL Kills Cells T Outside Inside Cytosol Golgi Apparatus A T B Endoplasmic Reticulum

  10. How EpCAMKDEL Kills Cells B T Outside Inside Cytosol Golgi Apparatus Endoplasmic Reticulum

  11. How EpCAMKDEL Kills Cells A T T Outside Inside Cytosol Golgi Apparatus A Endoplasmic Reticulum

  12. How EpCAMKDEL Kills Cells T Outside Inside Cytosol Golgi Apparatus Transport Vesicle Endoplasmic Reticulum A

  13. How EpCAMKDEL Kills Cells A T Outside Inside Cytosol Golgi Apparatus Endoplasmic Reticulum

  14. How EpCAMKDEL Kills Cells A T Outside Inside Cytosol Golgi Apparatus Endoplasmic Reticulum

  15. Conventional Immunotoxin Administration

  16. Cells Transfected With Immunotoxins Directly at the Site of The Tumor Therapy Targeted Directly at The Site Of The Tumor

  17. Transfecting EpCAMKDEL Immunotoxin DNA Into Cancerous Cells Using LNCX.NGFR

  18. Transfecting EpCAMKDEL Immunotoxin DNA Into Cancerous Cells Using LNCX.NGFR

  19. Transfecting EpCAMKDEL Immunotoxin DNA Into Cancerous Cells Using LNCX.NGFR

  20. Transfecting EpCAMKDEL Immunotoxin DNA Into Cancerous Cells Using LNCX.NGFR

  21. Transfecting EpCAMKDEL Immunotoxin DNA Into Cancerous Cells Using LNCX.NGFR

  22. Transfecting EpCAMKDEL Immunotoxin DNA Into Cancerous Cells Using LNCX.NGFR

  23. NIH-3T3 Transfected with EpCAMKDEL/LNCX.NGFR

  24. Proliferation Assay

  25. Proliferation Assay

  26. Conclusions • Immunotoxin genes were capable of transfection into mammalian cells. • The mammalian carrier cells were capable of expressing the immunotoxin genes. • Expressed immunotoxins were capable of killing cancerous cells. • The mouse cell lines tested were more capable of transfection than the human cell lines.

  27. Future Study • Testing in a live model (in vivo). • Use results in an effective cancer therapy for human.

  28. Acknowledgments • Team Research • Dr. Daniel Vallera • Dr. Deborah Todhunter • Ms. Lois Fruen

  29. Transfection of Recombinant Plasmid DNA From Immunotoxins into Eukaryotic Cells for the Development of an Antibody Targeted Carcinoma Therapy Egal Gorse 2006-2007

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