Gendicine

Gendicine is a recombinant adenovirus engineered to express wildtype-p53 (rAd-p53). This virus is designed to treat patients with tumors which have mutated p53 genes.

Gendicine is the first gene therapy product approved for clinical use in humans. Gendicine is manufactured by Shenzhen SiBiono GeneTech. Gendicine was approved in 2003 by the Chinese State Food and Drug Administration to treat head and neck squamous cell carcinoma.[1]

Gendicine enters the tumour cells by way of receptor-mediated endocytosis and begins to over-express genes coding for the p53 protein needed to fight the tumour.[2] Ad-p53 seems to act by stimulating the apoptotic pathway in tumour cells, which increases the expression of tumour suppressor genes and immune response factors (such as the ability of natural killer (NK) cells to exert “bystander” effects). It also decreases the expression of multi-drug resistance, vascular endothelial growth factor and matrix metalloproteinase-2 genes and blocking transcriptional survival signals.

This is no close correlation between p53 mutation status of the tumour cells and response to Ad-p53 treatment.[3] Ad-p53 appears to act synergistically with conventional treatments such as chemo- and radiotherapy. This synergy still exists in patients who were able to resist chemotherapy and radiotherapy. There are fewer side effects than conventional therapy.

Introgen's Advexin, a similar gene therapy that also uses adenovirus to deliver the p53 gene, was turned down by the FDA in 2008.[4]

References

  1. ↑ "China approves first gene therapy". Nature Biotechnology 22: 3–4. 2004. doi:10.1038/nbt0104-3. PMID 14704685.
  2. ↑ Peng, Zhaohui (May 1, 2004). "The Genesis of Gendicine: The Story Behind the First Gene Therapy". Biopharm International.
  3. ↑ Zhaohui Peng (2005). "Current Status of Gendicine in China: Recombinant Human Ad-p53 Agent for Treatment of Cancers" (PDF). Human Gene Therapy (16): 1016–1027.
  4. ↑ "Ark floats gene therapy's boat, for now". Nature Biotechnology 26 (26): 1057–1059. 2008. doi:10.1038/nbt1008-1057.


This article is issued from Wikipedia - version of the Sunday, December 27, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.