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Immunopreventive Effects against Murine H22 Hepatocellular Carcinoma in vivo by a DNA Vaccine Targeting a Gastrin-Releasing Peptide

  • Meko'o, Jean Louis Didier (School of Life Science and Technology, China Pharmaceutical University) ;
  • Xing, Yun (School of Life Science and Technology, China Pharmaceutical University) ;
  • Zhang, Huiyong (School of Life Science and Technology, China Pharmaceutical University) ;
  • Lu, Yong (School of Life Science and Technology, China Pharmaceutical University) ;
  • Wu, Jie (School of Life Science and Technology, China Pharmaceutical University) ;
  • Cao, Rongyue (School of Life Science and Technology, China Pharmaceutical University)
  • Published : 2014.11.06

Abstract

There is a continuing need for innovative alternative therapies for liver cancer. DNA vaccines for hormone/growth factor immune deprivation represent a feasible and attractive approach for cancer treatment. We reported a preventive effect of a DNA vaccine based on six copies of the B cell epitope GRP18-27 with optimized adjuvants against H22 hepatocarcinoma. Vaccination with pCR3.1-VS-HSP65-TP-GRP6-M2 (vaccine) elicited much higher level of anti-GRP antibodies and proved efficacious in preventing growth of transplanted hepatocarcinoma cells. The tumor size and weight were significantly lower (p<0.05) in the vaccine subgroup than in the control pCR3.1-VS-TP-HSP65-TP-GRP6, pCR3.1-VS-TP-HSP65-TP-M2 or saline subgroups. In addition, significant reduction of tumor-induced angiogenesis associated with intradermal tumors of H22 cells was observed. These potent effects may open ways towards the development of new immunotherapeutic approaches in the treatment of liver cancer.

Keywords

References

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