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  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)

Changes in blood vessel maturation in the fibrous cap of the tumor rim

https://doi.org/10.24517/00062980
https://doi.org/10.24517/00062980
20979207-fe58-4659-a79a-05cd12111a8f
名前 / ファイル ライセンス アクション
ME-PR-NAITO-H-433.pdf ME-PR-NAITO-H-433.pdf (1.3 MB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-07-05
タイトル
タイトル Changes in blood vessel maturation in the fibrous cap of the tumor rim
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
ID登録
ID登録 10.24517/00062980
ID登録タイプ JaLC
著者 Naito, Hisamichi

× Naito, Hisamichi

WEKO 99339
e-Rad 30570676

Naito, Hisamichi

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Takara, Kazuhiro

× Takara, Kazuhiro

WEKO 99305

Takara, Kazuhiro

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Wakabayashi, Taku

× Wakabayashi, Taku

WEKO 99293

Wakabayashi, Taku

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Kawahara, Hiroki

× Kawahara, Hiroki

WEKO 99328

Kawahara, Hiroki

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Kidoya, Hiroyasu

× Kidoya, Hiroyasu

WEKO 24114

Kidoya, Hiroyasu

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Takakura, Nobuyuki

× Takakura, Nobuyuki

WEKO 15659
e-Rad 80291954
研究者番号 80291954

Takakura, Nobuyuki

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著者別表示 内藤, 尚道

× 内藤, 尚道

内藤, 尚道

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高倉, 伸幸

× 高倉, 伸幸

高倉, 伸幸

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提供者所属
内容記述タイプ Other
内容記述 金沢大学医薬保健研究域医学系
書誌情報 Cancer Science

巻 103, 号 3, p. 433-438, 発行日 2011-11-20
ISSN
収録物識別子タイプ ISSN
収録物識別子 1347-9032
ISSN
収録物識別子タイプ ISSN
収録物識別子 1349-7006
NCID
収録物識別子タイプ NCID
収録物識別子 AA11808050
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1111/j.1349-7006.2011.02157.x
出版者
出版者 Japanese Cancer Association 日本癌学会 / wiley
抄録
内容記述タイプ Abstract
内容記述 It is widely accepted that blood vessels in the tumor microenvironment are immature because mural cell (MC) adhesion to endothelial cells (ECs) is broadly lacking. Hyperpermeability of the tumor vasculature then results in interstitial hypertension that mitigates against penetration of anticancer drugs into the depths of the tumor. It has been suggested that treatment with angiogenesis inhibitors normalizes blood vessels, resulting in restoration of normal permeability and improved drug delivery. However, recent reports suggest that cancer cell invasion is induced from the edge of the tumor into peripheral areas after treatment with angiogenesis inhibitors. Therefore, it is important to assess the status of blood vessels in the fibrous cap at the tumor rim after antiangiogenesis therapy. In the present study, we found that mature blood vessels in which ECs are covered with MCs are present in the fibrous cap. After treatment with angiogenesis inhibitors, immature blood vessels were destroyed and vascular function was significantly improved, but maturing blood vessels in which ECs were covered with MCs remained visible. These maturing blood vessels showed a less dilated character after treatment with the angiogenesis inhibitors. It is widely accepted that well-matured blood vessels are sheathed in extracellular matrix (ECM) and that cancer cells migrate along tracks made of ECM collagen fibers. Therefore, our data indicate the importance of destroying maturing blood vessels outside the tumor parenchyma to prevent cancer cell invasion. © 2011 Japanese Cancer Association.
権利
権利情報 copyright © 日本癌学会 Japanese Cancer Association
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連URI
識別子タイプ URI
関連識別子 http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1349-7006/
関連名称 http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1349-7006/
関連URI
識別子タイプ URI
関連識別子 https://onlinelibrary.wiley.com/doi/10.1111/j.1349-7006.2011.02157.x
関連名称 https://onlinelibrary.wiley.com/doi/10.1111/j.1349-7006.2011.02157.x
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