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  1. 20 医学系研究科・医学部
  2. 20C 本学関連学会刊行誌
  3. 20C1 秋田医学
  4. 第31巻1号

Modulation of Endothelial Cell Migration by Heparanase

http://hdl.handle.net/10295/1540
http://hdl.handle.net/10295/1540
d36090e3-614d-4c2d-ab3a-33a35bc7f8ff
名前 / ファイル ライセンス アクション
akigaku31-1h.pdf akigaku31-1h.pdf (576.6 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2009-01-18
タイトル
タイトル Modulation of Endothelial Cell Migration by Heparanase
言語 en
言語
言語 eng
主題
主題Scheme Other
主題 Heparanase
主題
主題Scheme Other
主題 HUVEC
主題
主題Scheme Other
主題 FGF
主題
主題Scheme Other
主題 VEGF
主題
主題Scheme Other
主題 heparan sulfate proteoglycan
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
作成者 HORIKAWA, Naoki

× HORIKAWA, Naoki

en HORIKAWA, Naoki

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内容記述
内容記述タイプ Abstract
内容記述 Cancer cells need new angiogenesis to grow and invade into new areas. A currently accepted model of angiogenesis associated with cancers involves growth factors, such as fibroblast growth factor (FGF) and vascular endothelial growth factor (VEGF), produced or induced by cancers stimulating endothelial cells in the surrounding tissue to from new blood vessels. Other molecules could also participate in the mechanism of angiogenesis by modulating growth factor activities. Heparan sulfate proteoglycan (HSPG) functions as one of such molecule by specifically binding to FGF and VEGF. Heparanase, an endo-fi-glucuronidase specifically degrading HSPG, has been reported in some cancers and implicated in the mechanism of metastasis. Since heparanase degrades HSPG and thus could modulate FGF and VEGF activities, the potential role of this enzyme in angiogenic mechanism was investigated. The migration of human umbilical vein endothelial cells (HUVECs) toward FGF and VEGF in the Boyden chamber was employed as a model system of angiogenesis. Addition of purified heparanase protein to the HUVEC culture significantly abrogated the FGF- and VEGF-induced cell migration. Reversal of this inhibitory activity of heparanase by heparin suggested that the effect involved degradation of HSPG. HUVEC transiently transfected with heparanase gene also exhibited suppressed migration toward FGF and VEGF. These results clearly demonstrated that heparanase in amounts sufficient to degrade cell surface HSPG abrogated the migration of HUVEC induced by FGF or VEGF_ The modulation of growth factor activities using heparanase may provide useful tools devising new cancer therapies.
言語 en
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
書誌情報 秋田医学

巻 31, 号 1, p. 83-93, 発行日 2004-05-01
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 03866106
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AN00009294
出版者
出版者 秋田医学会
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