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Expression and function of tetraspanin 1 in esophageal carcinoma.
Gu, Tingting; Chen, Weiwei; Chen, Li; Wang, Guilan; Li, Tiejun; Zhu, Yuanyuan; Gao, Xiaojiao.
Afiliação
  • Gu T; Department of Pathological Anatomy, Nantong University, Nantong, Jiangsu 226001, P.R. China.
  • Chen W; Department of Pathology, Affiliated Hospital of Jiangsu University, The First People's Hospital of Kunshan, Suzhou, Jiangsu 215300, P.R. China.
  • Chen L; Department of Pathological Anatomy, Nantong University, Nantong, Jiangsu 226001, P.R. China.
  • Wang G; Department of Pathological Anatomy, Nantong University, Nantong, Jiangsu 226001, P.R. China.
  • Li T; Department of Pathology, Affiliated Tumor Hospital, Nantong University, Nantong, Jiangsu 226001, P.R. China.
  • Zhu Y; Department of Pathological Anatomy, Nantong University, Nantong, Jiangsu 226001, P.R. China.
  • Gao X; Research and Development Department, Biomics Biotechnologies Co., Ltd., Nantong University, Nantong, Jiangsu 226016, P.R. China.
Oncol Lett ; 14(6): 6815-6822, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29422958
ABSTRACT
The present study explored the expression of tetraspanin 1 (TSPAN1) in esophageal carcinoma (EC) and its association with clinicopathological factors. TSPAN1 small interfering RNA (siRNA) was designed to target the TSPAN1 gene in Eca-109 cells in order to explore the biological function of TSPAN1 in the proliferation and apoptosis of EC. The results demonstrated that the level of TSPAN1 expression in EC tissue was significantly increased compared with that in adjacent normal tissue (P<0.001). TSPAN1 expression was also associated with histological differentiation, depth of invasion, lymph node metastasis (all P<0.05) and Ki-67 (P<0.01). However, no association was observed between TSPAN expression and gender, age or location (P>0.05). In addition, silencing TSPAN1 markedly inhibited proliferation while increasing the apoptosis rate of Eca-109 cells, which was demonstrated by detecting the expression of the cell proliferation-associated gene Ki-67 and the apoptotic gene caspase-3 (P<0.05). Taken together, these results indicated that TSPAN1 functions as a tumor-associated gene in EC through promoting cell proliferation and suppressing apoptosis, and siRNA technology may provide an advanced alternative in the development of therapeutics for EC.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article