期刊论文详细信息
Cancer Science
Suprabasin as a novel tumor endothelial cell marker
Mohammad T. Alam3  Hiroko Nagao-Kitamoto3  Noritaka Ohga3  Kosuke Akiyama3  Nako Maishi3  Taisuke Kawamoto3  Nobuo Shinohara1  Akinobu Taketomi2  Masanobu Shindoh4  Yasuhiro Hida5 
[1] Department of Renal and Genitourinary Surgery, Graduate School of Medicine, Hokkaido University, Sapporo, Japan;Department of Gastroenterological Surgery I, Graduate School of Medicine, Hokkaido University, Sapporo, Japan;Vascular Biology, Frontier Research Unit, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan;Department of Oral Pathology and Biology, Graduate School of Dental Medicine, Hokkaido University, Sapporo, Japan;Department of Cardiovascular and Thoracic Surgery, Graduate School of Medicine, Hokkaido University, Sapporo, Japan
关键词: Angiogenesis;    suprabasin;    suprabasin signaling;    tumor endothelial cell marker;    tumor endothelial cells;   
DOI  :  10.1111/cas.12549
来源: Wiley
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【 摘 要 】

Abstract

Recent studies have reported that stromal cells contribute to tumor progression. We previously demonstrated that tumor endothelial cells (TEC) characteristics were different from those of normal endothelial cells (NEC). Furthermore, we performed gene profile analysis in TEC and NEC, revealing that suprabasin (SBSN) was upregulated in TEC compared with NEC. However, its role in TEC is still unknown. Here we showed that SBSN expression was higher in isolated human and mouse TEC than in NEC. SBSN knockdown inhibited the migration and tube formation ability of TEC. We also showed that the AKT pathway was a downstream factor of SBSN. These findings suggest that SBSN is involved in the angiogenic potential of TEC and may be a novel TEC marker.

【 授权许可】

CC BY-NC-ND   
© 2014 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association.

Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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