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Xpention Genetics, Inc. is a biotechnology company that was formed to develop both immunological and molecular tests for cancer detection in animals and humans as well as therapeutic vaccines and other treatment methods for both veterinary and human cancers. Xpention through its subsidiary has licensed, exclusive rights to a specific genetic marker called the p65 that has highly specific correlation to numerous cancers.
 
     
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Following development of the molecular assay, the company will pursue development of therapeutic vaccines utilizing RNAi (interference RNA) technology. Any changes in the genetic dynamic of P65 will steer cells toward abnormal growth resulting in tumor development. The hallmark of P65 alteration is a pronounced increase in the level of gene expression. Other oncogenes such as ERB2 are found to be elevated primarily in breast cancer. It has been shown that once the level of ERB2 goes back to normal, cancer growth slows down or disappears.

Xpention’s approach to vaccine development relies on the use of RNAi technology. RNAi is a novel technique capable of manipulating the level of a target gene by “interfering” with its genetic expression. This technology has been successfully applied to a variety of genetic targets including cancer and viral genes. Xpention is developing adenoviral vector based delivery systems that contain genetic elements unique to P65 sequences. By interfering with the genetic machine responsible for the altered levels of P65 in cancer cells, Xpention aims to revert or slow down the neoplastic process. An “in vitro” and mouse model for P65 related cancer growth has already been developed. The company will also employ the “Integrated technology platform system” (ITPS) to determine the efficacy of adenovirus vector RNAi based vaccine (AVVRNAi). Levels of p65 are measured before and at different time points after AVVRNAi injections in mice. Different dosages of vaccine will be used to determine the proper concentrations based on the highest levels of P65 gene inhibition. ITPS will greatly expedite the preclinical stage of the P65 vaccine development allowing a faster and more efficient start of human clinical studies.

 


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