ログイン
言語:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Inhibitory effects of adhesion oligopeptides on the invasion of squamous carcinoma cells with special reference to implication of αv integrins

http://hdl.handle.net/2297/1661
http://hdl.handle.net/2297/1661
87badfcc-b81f-4023-b770-0397253e858e
名前 / ファイル ライセンス アクション
KawaharaJCRCO1995.pdf KawaharaJCRCO1995.pdf (72.4 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Inhibitory effects of adhesion oligopeptides on the invasion of squamous carcinoma cells with special reference to implication of αv integrins
言語
言語 eng
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
著者 Kawahara, Ei

× Kawahara, Ei

WEKO 661
e-Rad 90161348
研究者番号 90161348

Kawahara, Ei

Search repository
Imai, Kazushi

× Imai, Kazushi

WEKO 20611

Imai, Kazushi

Search repository
Kumagai, Shigehiro

× Kumagai, Shigehiro

WEKO 20612
e-Rad 00215013

Kumagai, Shigehiro

Search repository
Yamamoto, Etsuhide

× Yamamoto, Etsuhide

WEKO 157
e-Rad 00092445
金沢大学研究者情報 00092445
研究者番号 00092445

Yamamoto, Etsuhide

Search repository
Nakanishi, Isao

× Nakanishi, Isao

WEKO 20613

Nakanishi, Isao

Search repository
提供者所属
内容記述タイプ Other
内容記述 金沢大学大学院医学系研究科保健学専攻
書誌情報 Journal of Cancer Research and Clinical Oncology

巻 121, 号 3, p. 133-140, 発行日 1995-01-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0171-5216
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1007/bf01198094
出版者
出版者 Springer
抄録
内容記述タイプ Abstract
内容記述 We studied invasion-related adhesion events in vitro using three squamous carcinoma cell lines (HSC-3, poorly differentiated type; OSC-19, well-differentiated type; and KB cells, undifferentiated type). An in vitro invasion assay through matrigel in the transwell chamber revealed that HSC-3 cells were most invasive, OSC-19 cells moderately invasive and KB cells least invasive. Inhibition assay of invasion using synthetic peptides RGD, RGDV, RGDS, RGDT, IKVAV and YIGSR, showed that invasion of the three cell lines was significantly inhibited by RGDV. There were other peptides that inhibited invasion significantly including IKVAV for HSC-3, and RGDS and YIGSR for OSC-19. HSC-3 cells and OSC-19 cells adhered to fibronectin, laminin, vitronectin, and type IV collagen, and KB cells did not adhere to laminin but did to fibronectin, vitronectin and collagen type IV. Pretreatment of cells with RGDV peptide in the attachment assay reduced the ability of these cells to bind to vitronectin and fibronectin more efficiently than pretreatment with RGDS. Anti-αv antibodies inhibited adhesion of HSC-3, OSC-19 and KB cells to vitronectin, but anti-β1 antibodies did not inhibit adhesion. Immunofluorescent microscopic examinations showed that all cell lines were positive for anti-β5 and anti-αv antibodies, and only HSC-β3 cells were positive for antiβ-3 antibody. α5β1 was not clearly demonstrated in any of the cell lines. RGDV was the most effective inhibitor of squamous cell carcinoma invasion among the synthetic oligopeptides used in this experiment, and it is suggested that it affects αvβ3-and/or αvβ5-mediated carcinoma cell invasion.
権利
権利情報 The Original version is available at www.springerlink.com
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
戻る
0
views
See details
Views

Versions

Ver.1 2023-07-27 12:21:34.750506
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3