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. 2003;2003(1):35-47.
doi: 10.1155/S1110724303209037.

Gene Therapy Applications to Cancer Treatment

Gene Therapy Applications to Cancer Treatment

Susy M. Scholl et al. J Biomed Biotechnol. 2003.

Abstract

Over the past ten years significant advances have been made in the fields of gene therapy and tumour immunology, such that there now exists a considerable body of evidence validating the proof in the principle of gene therapy based cancer vaccines. While clinical benefit has so far been marginal, data from preclinical and early clinical trials of gene therapy combined with standard therapies are strongly suggestive of additional benefit. Many reasons have been proposed to explain the paucity of clinical responses to single agent vaccination strategies including the poor antigenicity of tumour cells and the development of tolerance through down-regulation of MHC, costimulatory, signal transduction, and other molecules essential for the generation of strong immune responses. In addition, there is now evidence from animal models that the growing tumour may actively inhibit the host immune response. Removal of the primary tumour prior to T cell transfer from the spleen of cancer bearing animals, led to effective tumour cell line specific immunity in the recipient mouse suggesting that there is an ongoing tumour-host interaction. This model also illustrates the potential difficulties of clinical vaccine trials in patients with advanced stage disease.

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References

    1. Ménétrier-Caux C, Montmain G, Dieu M C, et al. Inhibition of the differentiation of dendritic cells from CD34(+) progenitors by tumor cells: role of interleukin-6 and macrophage colony-stimulating factor. Blood. 1998;92(12):4778–4791. - PubMed
    1. Swisher S G, Roth J A, Carbone D P. Genetic and immunologic therapies for lung cancer. Semin Oncol. 2002;29(1 suppl 4):95–101. - PubMed
    1. Kigawa J, Sato S, Shimada M, Kanamori Y, Itamochi H, Terakawa N. Effect of p53 gene transfer and cisplatin in a peritonitis carcinomatosa model with p53-deficient ovarian cancer cells. Gynecol Oncol. 2002;84(2):210–215. - PubMed
    1. Ozols R F. Future directions in the treatment of ovarian cancer. Semin Oncol. 2002;29(1 suppl 1):32–42. - PubMed
    1. Xu M, Lin C, Liang X. Experimental study on combination of Ad-p53 with CDDP or As(2)O(3) in human lung adenocarcinoma cell line GLC-82 [in Chinese] Zhonghua Yi Xue Za Zhi. 2000;80(9):689–693. - PubMed