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タイトル
  • Receptor for Advanced Glycation End Products (RAGE) Functions as a Receptor for Specific Sulfated Glycosaminoglycans, and Anti-RAGE Antibody or The Sulfated Glycosaminoglycans Delivered in Vivo Inhibit Pulmonary Metastasis of Tumor Cells
作成者

Shuji, Mizumoto

NRID 1000040443973

Jun, Takahashi

Kazuyuki, Sugahara

NRID 1000060154449
権利情報
    • This research was originally published in JOURNAL OF BIOLOGICAL CHEMISTRY. : Shuji MIZUMOTO, Jun TAKAHASHI, Kazuyuki SUGAHARA. Receptor for Advanced Glycation End Products (RAGE) Functions as a Receptor for Specific Sulfated Glycosaminoglycans, and Anti-RAGE Antibody or The Sulfated Glycosaminoglycans Delivered in vivo Inhibit Pulmonary Metastasis of Tumor Cells. 2012; Vol.287(23) :18985-18994. © 2012 the American Society for Biochemistry and Molecular Biology.
主題
  • NDC 490
内容注記
Other
  • Altered expression of chondroitin sulfate (CS) and heparan sulfate (HS) at the surfaces of tumor cells plays a key role in malignant transformation and tumor metastasis. Previously we demonstrated that a Lewis lung carcinoma (LLC)-derived tumor cell line with high metastatic potential had a higher proportion of E-disaccharide units, GlcUA-GalNAc(4,6-O-disulfate), in CS chains than low metastatic LLC cells and that such CS chains are involved in the metastatic process. The metastasis was markedly inhibited by the pre-administration of CS-E from squid cartilage rich in E units or by preincubation with a phage display antibody specific for CS-E. However, the molecular mechanism of the inhibition remains to be investigated. In this study the receptor molecule for CS chains containing E-disaccharides expressed on LLC cells was revealed to be receptor for advanced glycation end products (RAGE), which is a member of the immunoglobulin superfamily predominantly expressed in the lung. Interestingly, RAGE bound strongly to not only E-disaccharide, but also HS-expressing LLC cells. Furthermore, the colonization of the lungs by LLC cells was effectively inhibited by the blocking of CS or HS chains at the tumor cell surface with an anti-RAGE antibody through intravenous injections in a dose-dependent manner. These results provide the clear evidence that RAGE is at least one of the critical receptors for CS and HS chains expressed at the tumor cell surface and involved in experimental lung metastasis and that CS/HS and RAGE are potential molecular targets in the treatment of pulmonary metastasis.
出版者American Society for Biochemistry and Molecular Biology
日付 Issued 2012-06-01
言語eng
資源タイプjournal article
出版タイプAM
資源識別子 URI http://hdl.handle.net/2115/49329
関連
  • isIdenticalTo DOI https://doi.org/10.1074/jbc.M111.313437
収録誌情報
    • ISSN 0021-9258
    • ISSN 1083-351X
    • The Journal of Biological Chemistry
    287(23), 18985-18994
ファイル
コンテンツ更新日時2019-10-09T00:14:31Z