Globular adiponectin, acting via adiponectin receptor-1, inhibits leptin-stimulated oesophageal adenocarcinoma cell proliferation

被引:71
作者
Ogunwobi, Olorunseun O. [1 ]
Beales, Ian L. P. [1 ,2 ]
机构
[1] Univ E Anglia, Sch Med Hlth Policy & Practice, Ctr Biomed Res, Norwich NR4 7TJ, Norfolk, England
[2] Norfolk & Norwich Univ Hosp, Dept Gastroenterol, Norwich NR4 7UZ, Norfolk, England
关键词
adiponectin; AMP-activated kinase; cell proliferation; leptin; obesity; oesophageal adenocarcinoma; phosphoprotein phosphatase;
D O I
10.1016/j.mce.2008.01.023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Obesity increases the risk of developing several cancers including oesophageal adenocarcinoma (OAC). Obesity is characterised by hyperleptinaema and hypoadiponectinaemia: we have hypothesised that these hormonal factors may contribute to the progression of OAC. We have examined the effects of leptin and adiponectin on proliferation of OAC cells. Leptin-stimulated proliferation in four different OAC lines (OE33, OE19, BIC-1 and FLO) and this was inhibited by globular but not full length adiponectin. All four OAC lines expressed both adiponectin-receptor isoforms (AdipoR1 and AdipoR2). Globular adiponectin also inhibited leptin-induced proliferation in rat IEC-18 cells which only expressed AdipoR1. Specific inhibitors of 5-AMP-activated protein kinase (Compound Q and serine/threonine phosphatases (okadaic acid) and a specific siRNA to AdipoR1 blocked the anti-proliferative effects of adiponectin. Adiponectin inhibited leptin-induced Akt phosphorylation; this action was sensitive to okadaic acid but not to Compound C. Adiponectin deficiency may contribute to the promotion of OAC in obesity. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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