One of the biggest risks to world health is cancer, and because of its complexity and diversity, traditional therapies like radiation therapy, chemotherapy, and surgery can sometimes be ineffective. A developing therapeutic approach called gene therapy seeks to treat cancer by deleting, replacing, or repairing damaged genes. In addition to focusing on the tumor cells, this strategy enhances the patient's immune system, which leads to a better treatment effect. We have extensive research and service expertise in developing cancer gene therapy formulations, and CD Formulation is a leader in the creation of gene therapy drugs.
The genomic characteristics of cancer provide the possibility of personalized treatment. By analyzing the genomic information of tumor cells, a treatment plan for a specific type of cancer is issued. Gene therapy can reduce damage to normal cells, reduce side effects, and improve patients' quality of life. In addition, as technology continues to advance, the safety and efficacy of gene therapy continues to improve.
CTGVT is to insert anticancer genes into oncolytic virus (OV) vectors. By combining the respective advantages of gene therapy and viral therapy, the viral vectors can specifically replicate in tumor cells and kill tumor cells in a targeted manner. By combining the respective advantages of gene therapy and virus therapy, the viral vector itself can specifically replicate in the tumor cells and kill the tumor cells in a targeted manner, and on the other hand, the expression of the exogenous genes it carries can be greatly increased with the replication and proliferation of the viral vector, which can overcome the drawbacks of low transfection efficiency, poor targeting, low expression of anticancer genes, and insufficient killing power of the traditional cancer gene therapy.
RNA interference (RNAi) is a sequence-specific post-transcriptional gene silencing (PTGS) mechanism wherein double-stranded RNA (dsRNA) molecules mute the matching genes at the mRNA level or stop their expression. RNA interference (RNAi) technology is currently being used more and more in cancer research. In tumor therapy, RNAi technology can specifically inhibit the expression of non-normally up-regulated cancer-related genes, so that they are silenced or dormant, and then achieve the purpose of inhibiting the growth of tumor cells.
Immunogene therapy uses genetically modified tumor seedlings or antigen-presenting cells in vitro, or the direct introduction of immunogenes in vivo,to stimulate or enhance the anti-tumor immune function of the human body, so as to achieve the purpose of tumor treatment. Therapeutic genes include tumor-associated antigen genes, cytokine genes, or MHC genes.
CD Formulation is redefining the gold standard in gene therapy formulation development, with each of our experimental protocols validated by real-world data. If you are interested in us, please feel free to contact us.