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1999 Fiscal Year Final Research Report Summary

Development of a method for combination electro-gene therapy using suicide gene and chemokine gene(s)

Research Project

Project/Area Number 10671309
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Cerebral neurosurgery
Research InstitutionKUMAMOTO UNIVERSITY

Principal Investigator

NISHI Toru  KUMAMOTO UNIV.HOSP. INSTRACTOR, 医学部・附属病院, 助手 (00264309)

Co-Investigator(Kenkyū-buntansha) TAKESHIMA Hideo  KUMAMOTO UNIV. MED.SCH. INSTRACTOR, 医学部, 助手 (70244134)
KOCHI Masato  KUMAMOTO UNIV. MED.SCH. ASSOCIATE PROFESSOR, 医学部, 助教授 (70178218)
USHIO Yukitaka  KUMAMOTO UNIV. MED.SCH. PROFESSOR, 医学部, 教授 (20028583)
Project Period (FY) 1998 – 1999
Keywordselectro-gene therapy / gene therapy / suicide gene / chemokine gene / CT26 tumor
Research Abstract

1. Electro-gene therapy using suicide genes.
We could develop a method for successful electro-gene therapy (EGT) using plasmid DNA for tumor bearing mice. Subcutaneously inoculated CT26 tumor was subjected to EGT, which consists of intratumoral injection of a naked plasmid encoding a marker gene or a therapeutic gene, followed by in vivo electroporation (EP). When this treatment modality is carried out with the plasmid DNA for the green fluorescent protein gene, followed by in vivo EP with the optimized pulse parameters, numerous intensely bright green fluorescent signals appeared within the tumor. EGT, using the 'A' fragment of the diphtheria toxin gene significantly inhibited the growth of tumors, by about 30%, on the flank of mice. With the herpes simplex virus thymidine kinase gene, followed by systemic injection of ganciclovir, EGT was far more effective in retarding tumor growth, varying between 50%-90%, compared to the other controls. Based on these results, it appears that EGT c … More an be successfully used for treating murine solid tumors.
2. Combination electro-gene therapy using suicide gene and chemokine gene.
As next step, we performed a combiantion electro-gene therapy using a suicide gene and cytokine gene. We selected HS-tk gene and IL-12 gene for this study, since the usage of both genes in gene therapy for malignant tumor has been established and the mechanisms for the effect is already known. We constructed two expression plasmids for two subunits of IL-12. Three expression plasmid DNAs for HS-tk, p40 and p30 were mixed and injected into subucutaneous tumors, followed by in vivo electroporation. The anti-tumor effect of combination electro-gene therapy was significantly stronger than those of single gene therapy. In animals in which tumor was totally eradicated, the establishment of systemic anti-tumor immunity was confirmed by rechallenge experiments.
We think this method for in vivo gene transfer and gene therapy for malignant solid tumors are very efficient and have possible applications to all kinds or solid tumors. Less

  • Research Products

    (32 results)

All Other

All Publications (32 results)

  • [Publications] Yoshizato K: "Gene delivery with optimized electroporation parameters shows potential for treatmeant of gliomas"Int. Natl. J. Oncol.. 15(in press). (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Goto T: "Highly efficient Electro-gene therapy of solid tumor using an expression plasmid for HS-tk gene"Proc. Natl. Acad. Sci. USA. 97. 354-359 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 西 徹: "in vivo electroporationの遺伝子治療への応用"細胞工学. (in press). (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamamoto K: "Cloning and Functional Characterization of the 5'-Flaking Region of the human Monocyte Chemoattractant Protein-1 Receptor (CCR2) Gene. Essential role of 5'-untranslated region in tissue specific expression"J. Biol. Chem.. 274. 4646-4654 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nishi T: "Prognostic Significance of the MIB-1 labeling Index for Patient with Craniopharyngioma"Int. Natl. J. Mol. Med.. 3. 157-161 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Sato K: "Expression of 120 nucleolar proliferating antigen in human glicomas and growth suppression of glioma cells by p120 ribozyme vector"Int. Natl. J. Oncol.. 14. 417-424 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yuji Oshima: "Target gene transfer to corneal endothelin in vivo by electric pulse"Gene Therapy. 5. 1347-1354 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Hideo Takeshima: "Loss of merlin-p85 protein complex in NF2-related tumors"International Journal of Oncology. 12. 1073-1078 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Koga H: "Impairment of cell adhesion by expression of the mutant neurofibromatosis type 2 (NF2) gene which lack exons in the ERM-homology domain"Oncogene. 17. 801-810 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Korematsu K: "Cadherin 8 protein expression in grey matter structures and nerve fibers of the neonatal and adult mouse brain"Neuroscience. 87. 303-315 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Okamura A: "Overexpression of stiatal enriched phosphatase (STEP) promotes the neurite outgrowth induced by a cATP analogue in PC12 cells"Mol. Brain. Res.. 67. 1-9 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nishi T: "Tissue factor expressed in pituitary adenoma cells contributes to development of vascular events in adenomas"Cancer. 86. 1354-61 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 木村貴弘: "ヒト悪性グリオーマにおけるリンパ球特異的CCケモカインの発現"神経免疫研究. (in press). (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takeshima, H: "Monocyte chemoattractant protein-1 (MCP-1) derived from human maligant glioma Biological meanings of its expression and application for the treatment of malignant glioma"Research trends in Immunology. 2. 187-194 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takahiro Fukumoto: "Peptide mimics of the CTLA4-binding domain stimulate T-cell proliferation"Nature Biotech. 16. 267-270 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Oiso, M: "Differential binding of peptides substituted at aputative C-terminal anchor residue to I-Ag7b56hisb57Ser and I-Ag7b56Prob57asp"Immunogenetics. 47. 411-414 (1998)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nishi T: "Reporter/Functional Gene Transfer in Rat Brain. in Methods in Molecular Medicine, Vol 37: Electrically Mediated Delivery of Molecules to Cells"Humana Press, Inc. Totowa. 339-348 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yoshizato K: "Gene delivery with optimized electroporation parameters shows potential for treatment of gliomas"Int. Natl. J. Oncol.. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tomoaki Goto: "Highly efficient Electro-gene therapy of solid tumor using an expression plasmid for HS-tk gene"Proc Natl Acad Sci USA. 97. 354-359 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Keizo Yamamoto: "Cloning and Functional Characterization of the 5'-flanking Region of the Human Monocyte Chemoattractant Protein-1 Receptor(CCR2) Gene"The Journal of Biological Chemistry. 274. 4646-4654 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Toru Nishi: "Prognostic significance of the MIB-1 labeling index for patient with cranioparyngioma"International Journal of Molecular Medicine. 3. 157-161 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kyoichi Sato: "Expression of p120 nucleolar proliferating antigen in human gliomas and growth suppression of glioma cells by p120 ribozyme vector"International. Journal of Oncology. 14. 417-424 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Okamura A: "Overexpression of striatal enriched phosphatase (STEP) promotes the neurite outgrowth induced by a cAMP analogue in PC12 cells"Mol. Brain. Res.. 67. 1354-1361 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Toru Nishi: "Tissue factor expressed in pituitary adenoma cells contributes to development of vascular events in adenomas"Cancer. 86. 1354-1361 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hideo Takeshima: "Monocyte chemoattractant protein-1 (MCP-1) derived from human malignant glioma. -Biological meanings of its expression and application for the treatment of malignant glioma"Research Trends in Immunology. 2. 187-194 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takahiro Fukumoto: "Peptide mimics of the CTLA4-binding domain stimulate T-cell proliferation"Nature Biotech. 16. 267-270 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Oiso, M: "Differential blinding of peptides substituted at a putative C-terminal anchor residue to I-Ag7b56Hisb57Ser and I-Ag7b56Prob57Asp"Immunogenetics. 47. 411-414 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yuji Oshima: "Target gene transfer to corneal endothelium in vivo by electric pulse"Gene Therapy. 5. 1347-1354 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hideo Takeshima: "Loss of merlin-p85 protein complex in NF2-related tumors"International. Journal of Oncology. 12. 1073-1078 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Koga H: "Impairment of cell adhesion by expression of the mutant neurofibromatosis type 2 (NF2) gene which lack exons in the ERM-homology domain"Oncogene. 17. 801-810 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Korematsu K: "Cadherin 8 protein expression in grey matter structures and nerve fibers of the neonatal and adult mouse brain"Neuroscience. 87. 303-315 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] T.Nishi: "Reporter/Functional Gene Transfer in Rat Brain. Methods in Molecular Medicine, Vol 37: Electrically Mediated Delivery of Molecules to Cells"M.J.Jaroszeski, R.Helle&R.Gilbert (eds) Humana Press, Inc. Totowa. 339-348 (1999)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2001-10-23  

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