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)

Clinicopathological significance of platelet-derived growth factor (PDGF)-B and vascular endothelial growth factor-A expression, PDGF receptor-β phosphorylation, and microvessel density in gastric cancer

http://hdl.handle.net/2297/30295
http://hdl.handle.net/2297/30295
4504e3a7-73f0-4ac7-aace-8ce42d439f00
名前 / ファイル ライセンス アクション
ME-PR-SUZUKI-S-659.pdf ME-PR-SUZUKI-S-659.pdf (4.0 MB)
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 Clinicopathological significance of platelet-derived growth factor (PDGF)-B and vascular endothelial growth factor-A expression, PDGF receptor-β phosphorylation, and microvessel density in gastric cancer
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 Suzuki, Shioto

× Suzuki, Shioto

WEKO 572
e-Rad 40334859
研究者番号 40334859

Suzuki, Shioto

Search repository
Dobashi, Yoh

× Dobashi, Yoh

WEKO 22858

Dobashi, Yoh

Search repository
Hatakeyama, Yayoi

× Hatakeyama, Yayoi

WEKO 22859

Hatakeyama, Yayoi

Search repository
Tajiri, Ryosuke

× Tajiri, Ryosuke

WEKO 914
研究者番号 10402059

Tajiri, Ryosuke

Search repository
Fujimura, Takashi

× Fujimura, Takashi

WEKO 22001
研究者番号 50262580

Fujimura, Takashi

Search repository
Heldin, Carl H.

× Heldin, Carl H.

WEKO 22860

Heldin, Carl H.

Search repository
Ooi, Akishi

× Ooi, Akishi

WEKO 245
e-Rad 50160411
金沢大学研究者情報 50160411
研究者番号 50160411

Ooi, Akishi

Search repository
書誌情報 BMC Cancer

巻 10, p. 659, 発行日 2010-11-30
ISSN
収録物識別子タイプ ISSN
収録物識別子 1471-2407
NCID
収録物識別子タイプ NCID
収録物識別子 AA12034763
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1246/bcsj.20100168
出版者
出版者 BioMed Central
抄録
内容記述タイプ Abstract
内容記述 Background: Angiogenesis is important in the growth and metastasis of various kinds of solid tumors, including gastric cancers. The angiogenic process is triggered by several key growth factors, including vascular endothelial growth factor (VEGF)-A and platelet-derived growth factor (PDGF)-B, that are secreted by tumors. Our aim was to define: i) the expression pattern of VEGF-A and PDGF-B in tumor cells and the activation of PDGF receptor (PDGFR)-β tyrosine kinase in stromal cells of human gastric adenocarcinomas; and ii) the relationship between VEGF-A and PDGF-B expression and microvessel density (MVD), to determine if there is a rationale for a new therapeutic strategy.Methods: A series of 109 gastric adenocarcinoma cases that had undergone surgical resection was examined immunohistochemically using antibodies against VEGF-A, PDGF-B, and CD34, followed by further examination of PDGFR-β phosphorylation by immunoblotting analysis.Results: MVD was higher in diffuse-type than intestinal-type cancers (p < 0.001). VEGF-A overexpression correlated to PDGF-B overexpression in both the intestinal-type (p < 0.005) and diffuse-type (p < 0.0001) groups, indicating that VEGF-A and PDGF-B are secreted simultaneously in the same tumor, and may thus play important roles together in angiogenesis. However, several differences between intestinal-type and diffuse-type cancers were observed. In the diffuse-type cancer group, higher MVD was related to the PDGF-B proportion (p < 0.05) and VEGF-A overexpression (p < 0.05), but not to PDGF-B overexpression or the VEGF-A proportion. On the other hand, in the intestinal-type cancer group, higher MVD was correlated to overexpression (p < 0.005), intensity (p < 0.05), and proportion (p < 0.05) of PDGF-B, but not of VEGF-A. In addition, phosphorylation of PDGFR-β was correlated with depth of cancer invasion at statistically significant level.Conclusions: Our results indicate that PDGF-B, which is involved in the maintenance of microvessels, plays a more important role in angiogenesis in intestinal-type gastric carcinomas than VEGF-A, which plays a key role mainly in the initiation of new blood vessel formation. In contrast, VEGF-A has a critical role for angiogenesis more in diffuse-type cancers, but less in those of intestinal type. Thus, a therapy targeting the PDGF-B signaling pathway could be effective for intestinal-type gastric carcinoma, whereas targeting VEGF-A or both VEGF-A and PDGF-B signaling pathways could be effective for diffuse-type gastric carcinomas. © 2010 Suzuki et al; licensee BioMed Central Ltd.
権利
権利情報 © 2010 Suzuki et al; licensee BioMed Central Ltd.
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://www.biomedcentral.com/1471-2407/10/659
戻る
0
views
See details
Views

Versions

Ver.1 2023-07-28 01:00:27.585729
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