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2002 Fiscal Year Final Research Report Summary

Identification of intracellular target molecules of glyco-genes and functional glycomics for those proteins

Research Project

Project/Area Number 13670121
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General medical chemistry
Research InstitutionOsaka University

Principal Investigator

MIYOSHI Eiji  Osaka University Graduate School of Medicine Div. Biochemistry, Associate Professor, 医学部, 助教授 (20322183)

Project Period (FY) 2001 – 2002
KeywordsHepatocellular carcinoma / Haptoglobin / two-dimensional electrophoresis / GnT-III / GnT-V / Matriptase / Cancer Metastasis / Glycomics
Research Abstract

I identified intracellular target proteins for GnT-III and GnT-V and analyzed functions of those proteins. When DEN was administered to GnT-III transgenic mice, tumor formation in the liver was dramatically suppressed as compared to control mice. However, a few number of GnT-III transgenic mice treated with DEN had tumors. When serum proteins of those mice were analyzed by two-dimensional ectrophoresis followed by lectin blot, 6 target proteins for GnT-III were identified. One of these proteins was haptoglobin beta- chain. Haptoglobin is a radical scavenger and its function in terms of aberrant glycosylation should be clarified (Free Radical Research 36, 327-833, 2002). I also identified matriptase as a target molecule for GnT-V. Matriptase is one of membrane-anchored serine-protease, which has recently cloned. When GnT-V was transfected into a human gastric cancer cell MKN45, experimental metastasis was markedly promoted. The mechanism was due to induction of matriptase secretion because matriptase bearing beta1-6 GlcNAc branching, a product of GnT-V had a prolongation for degradation. This is the first answer for a question why GnT-V promotes cancer metastasis.

  • Research Products

    (10 results)

All Other

All Publications (10 results)

  • [Publications] Kitada, T., Miyoshi, E., et al.: "Addition of bisecting N-acetylglucosamine residues to E-cadherin downregulates the tyrosine phosphorylation of β-catenin"J. Biol. Chem.. 276. 475-480 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Chakraborty A K, Miyoshi E, et al.: "Fusion-Hybrids with macrophage and melanoma cells up-regulate N-acetylglucosaminyltransferase V, β1-6 branching, and metastasis"Cell Growth and Differentiation. 12. 623-630 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ekuni A, Miyoshi E et al.: "A glycomic approach to hepatic tumors in N-acetylglucosaminyltransferase III (GnT-III) transgenic mice induced by diethylnitorsamine (DEN) : Identification of haptoglobin as a target molecule of GnT-III"Free Radical Research. 36. 827-833 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ihara S, Miyoshi E, et al.: "Prometastatic effect of N-acetylglucosaminyltransferase V is due to modification and stabilization of active matriptase by adding beta 1-6 GlcNAc branching"J. Biol. Chem.. 277. 16960-16967 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Saito T, Miyoshi E, et al.: "A secreted type of beta 1,6-N-acetylglucosaminyltransferase V (GnT-V) induces tumor angiogenesis without mediation of glycosylation. A novel function of GnT-V distinct from the original glycosyltransferase"J. Biol. Chem.. 277. 17002-17008 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kitada, T. Miyoshi. E., Noda, K., Higashiyama, S., Ihara, H., Matsuura, N., Hayashi, N., Kawata, S., Matsuzawa, Y., and Taniguchi N.: "Addition of bisecting N-acetylglucosamine residues to: E-cadherin downregulates the tyrosine phosphotylation of β-catenin"J. Biol. Chem.. 276. 475-480 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Chakraborty A K, Pawelek J, Ikeda Y, Miyoshi E, Kolesnikova N, Funasaka Y, Ichihashi M, and Taniguchi N.: "Fusion-Hybrids with macrophage and melanoma cells up-regulate N-acetylglucosaminyltransferase V, β1-6 branching, and metastasis"Cell Growth and Differentiation. 12. 623-630 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ekuni A, Miyoshi E. Ko J H, Noda K, Kitada T, Ihara S, Endo T, Hino A, Honke K, and Taniguchi N: "A glycomic approach to hepatic tumors in N-acetylglucosaminyltransferase III (GnT-III) transgenic mice induced by diethylnitorsamine (DEN): Identification of haptoglobin as a target molecule of GnT-III"Free Radical Research. 36. 827-833 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ihara S, Miyoshi E, Ko JH, Murata K, Nakahara S, Honke K, Dickspn RB, Lin CY, Taniguchi N: "Prometastatic effect of N-acetylglucosaminyltransferase V is due to modification and stabilization of active matriptase by adding β 1-6 GlcNAc branching"J. Biol. Chem.. 277. 16960-16967 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Saito T, Miyoshi E, Sasai K, Nakano N, Eguchi H, Honke K, Taniguchi N: "A secreted type of β 1,6-N-acetylglucosaminyltransferase V (GnT-V) induces tumor angiogenesis without mediation of glycosylation. A novel function of GnT-V distinct from the original glycosyltransferase"J. Biol. Chem.. 277. 17002-17008 (2002)

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

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Published: 2004-04-14  

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