1 / 24

Cancer Gene Therapy

Cancer Gene Therapy. …Using Tumor Suppressor Genes. Overview. Gene Therapy p53 Using Gene Therapy to Treat Lung Cancer Problems. Gene Therapy. Vectors In Vivo vs. Ex Vivo Which cells are the target cells. What is Gene Therapy?.

Télécharger la présentation

Cancer Gene Therapy

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Cancer Gene Therapy …Using Tumor Suppressor Genes.

  2. Overview • Gene Therapy • p53 • Using Gene Therapy to Treat Lung Cancer • Problems

  3. Gene Therapy • Vectors • In Vivo vs. Ex Vivo • Which cells are the target cells

  4. What is Gene Therapy? • Gene therapy is a technique for introducing the genetic material of a gene in a patient that lacks that gene because of a mutation.

  5. Vectors • The way you insert the “normal” gene in the patient’s cell is by vectors. • The most common vectors that are used in gene therapy are virus vectors

  6. Why Viruses? • Viruses through the time of evolution have evolved to infect the cells with great specificity • Viruses tend to be very efficient at transfecting their own DNA into the host cell genome. • This allows them to produce new viral particles at the period of synthesis of the cell

  7. Types Of Viruses… • Retrovirus • Adinovirus • Lentiviruses • Poxviruses • and Herpes Viruses

  8. Adenovirus 36 kb Double Stranded DNA Genome Entry through CAR receptor and integrin co-receptor

  9. ITR Stuffer DNA Therapeutic Transgene Stuffer DNA ITR  L4 L1 L2 L3 L5 E1A E1B E3 E2B E2A E4 Latest Generation Adenoviral Vector “Gutless”; Helper-dependent; Minimal Ad

  10. Which Virus to Use? • Depends • how well they transfer the genes to cells • which cells they can recognize and infect • and whether they alter the cell’s DNA permanently or temporarily

  11. Strategies for Transgene Delivery Ex Vivo In Vivo Cells removed from body Transgene delivered directly into host Transgene delivered Cells cultured Cells returned to the body

  12. Which cells are the target cells • Both Healthy and Cancerous cells can be a target • Ex of targeting Healthy cells • One way is by replacing a missing or altered gene with a “normal” one

  13. Cont: Which cells are the target cells • Ex of targeting Cancer Cells • Scientists can target cancer cells with genes that can be used to destroy the cells. In this technique, cancer cells are introduced to what is called “suicide genes”

  14. Gene Therapy Principles AAV Nucleus Adenovirus Therapeutic Protein Retrovirus/Lentivirus Target Cell Naked DNA

  15. Adenovirus Cell Entry

  16. p53 Pathway

  17. Using Gene Therapy to Treat Lung Cancer • In this clinical trial the scientist used gene therapy in combination with radiation therapy so they can treat lung cancer in 19 different patients

  18. Treatment: Gene therapy and Radiation. • Intratumoral needle injections of Ad-p53 on days 1, 18 and 32 of the treatment. • tumors ≥ 4 cm where injected with 10 ml • tumors ‹ 4 cm were injected with 3 ml • Radiation therapy

  19. Results • 17/19 patients made it through the entire therapy • complete response in 2 patients (11%) • partial response in 4 patients (21%) • stable disease in 1 patient (5%) • progressive disease in 11 patients (57%)

  20. Results Not That Good • 57% of the patients showed that the cancer progressed to worse stages • Why?

  21. Major Problems that Scientists Must Overcome • Identify more efficient ways to deliver the genes to the patients’ genetic material • Develop vectors that can specifically focus on the targeted cells • Ensure that vectors will successfully insert the desired genes into each of these target cells

  22. Cont: Major Problems that Scientists Must Overcome • Deliver genes to a precise location in the patient’s DNA • Ensure that transplanted genes are precisely controlled by the body’s normal physiologic signals

More Related