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Suprabasin as a novel tumor endothelial cell marker

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 s...

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Detalles Bibliográficos
Autores principales: Alam, Mohammad T, Nagao-Kitamoto, Hiroko, Ohga, Noritaka, Akiyama, Kosuke, Maishi, Nako, Kawamoto, Taisuke, Shinohara, Nobuo, Taketomi, Akinobu, Shindoh, Masanobu, Hida, Yasuhiro, Hida, Kyoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317965/
https://www.ncbi.nlm.nih.gov/pubmed/25283635
http://dx.doi.org/10.1111/cas.12549
Descripción
Sumario: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.