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2000 Fiscal Year Final Research Report Summary

ESTABLISHMENT AND APPLIANCE OF NEWLY GENE THERAPY FOR DEGENERATIVE ARTHROSIS USING DECOY STRATEGY

Research Project

Project/Area Number 11470440
Research Category

Grant-in-Aid for Scientific Research (B).

Allocation TypeSingle-year Grants
Section一般
Research Field Surgical dentistry
Research InstitutionKYUSHU UNIVERSITY

Principal Investigator

TAKENOSHITA Yasuharu  KYUSHU UNIVERSITY GRADUATE SCHOOL OF DENTAL SCIENCE, ASS PROF, 歯学研究院, 助教授 (50117157)

Co-Investigator(Kenkyū-buntansha) KUBOTA Yasutaka  KYUSHU UNIVERSITY GRADUATE SCHOOL OF DENTAL SCIENCE, ASS PROF, 歯学研究院, 助手 (60205151)
NAKAGAWA Kazunori  KYUSHU UNIVERSITY GRADUATE SCHOOL OF MEDICAL SCIENCE, ASS PROF, 医学研究院, 講師 (50217668)
ISHIBASHI Hiroaki  KYUSHU UNIVERSITY GRADUATE SCHOOL OF DENTAL SCIENCE, ASS PROF, 歯学研究院, 助手 (90254630)
Project Period (FY) 1999 – 2000
KeywordsTEMPOROMANDIBULAR JOINT / EXTRACELLULAR MATRIX / GENE THERAPY
Research Abstract

(l) Examination for the expression of uPA and MMPs stimulated by several cytokines using cultured cells.
The expression of uPA and MMPs was increased by the stimulation with TNFα using cultured cells derived from cartilaginous tissue of TMJ.
(2) Examination of transcriptional factor related to cytokines stimulation. Transcriptional factors, NF-kB and Sp1, were activated by TNFα stimulation at the cultured cells derived from cartilaginous tissue.
(3) Establishment of the condition for the gene transfer
We established the condition for the Decoy oligodeoxynucletides targeted to NF-kB and Sp1 using HVJ-liposome method, and decoy ODNs were routinely transferred to 1OO % of the cells.
(4) Inhibition of the expression of uPA and MMPs by Decoy ODNs transfection
The expression of the uPA and MMPs were inhibited by the transfection of Decoy ODNs to the cultured cells derived from cartilaginous tissue.

  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] Ishibashi H, et al.: "Sp1 Decoy Transfected Cells Suppresses the Expression of VEGF, TGFβ1, and Tissue Facotr and also Cell Grwoth and Invasion Activites."Cancer Research. 60. 6531-6536 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ishibashi H, et al.: "Hypoxia-Induced Angiogenesis of Cultured Human Salivary Gland Carcinoma Cells Involves Enhancement VEGF Production and bFGF Release."Oral Oncology. (発表予定).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nakagawa K, et al.: "Angiogenesis and Its Regulation ; Role of VEGF."Semin Thromb Hemost.. 143. 201-206 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kubota Y, et al.: "Interleukin-1α-dependent Regulation of Matrixiz Matalloproteinase-9 (MMP-9) Secretion and Activation in the Epithelial Cells of Odontogenic Jaw Cysts."Journal of Dental Research. 79(6). 1423-1430 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] H.Ishibashi, et al: "Sp1 Decoy Transfected Cells Suppresses the Expression of VEGF, TGFβ1, and Tissue Facotr and also Cell Grwoth and Invasion Activites."Cancer Research. 60. 6531-6536 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] H.Ishibashi, et al: "Hypoxia-Induced Angiogenesis of Cultured Human Salivary Gland Carcinoma Cells Involves Enhancement VEGF Production and bFGF R elease."Oral Oncology. 37. 77-83 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Y.Kubota, et al: "Interleukin-1 α-dependent Regulation of Matrix Metalloproteinase-9 (MMP-9) Secretion and Activation in the Epithelial Cells of Odontogenic Jaw Cysts."Journal of Dental Research. 79 (6). 1423-1430 (2000)

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

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Published: 2002-03-26  

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