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作 者:冯睿婷 梅家转[1] 栗敏[1] 赵继智[1] 白桦[1] 刘桂举
机构地区:[1]郑州人民医院肿瘤内科,河南省郑州市450003
出 处:《世界华人消化杂志》2015年第8期1218-1223,共6页World Chinese Journal of Digestology
摘 要:目的:本研究观察脑源性神经营养因子(brain-derived neurotrophic factor,BDNF)对食管癌细胞株ECa9706体外增殖和迁移能力的影响以及机制.方法:采用MTT和Transwell方法分别观察BDNF以及酪氨酸激酶受体B(tyrosine kinase receptor B,Trk B)抑制剂K252a对ECa9706细胞增殖和迁移能力的影响,采用实时定量聚合酶链反应(real-time quantitative polymerase chain reaction,q PCR)和Western blot方法分别检测ECa9706细胞中Trk B和磷脂酶C(phospholipase C,PLC)-γ1的m RNA和蛋白表达水平.结果:BDNF可显著促进ECa9706细胞增殖和迁移能力,该作用可被K252a拮抗.与对照组相比,BDNF可诱导Trk B的m RNA和蛋白表达显著增加,并提高PLC-γ1的蛋白表达水平.结论:BDNF/Trk B/PLC-γ1在食管癌细胞迁移浸润中具有重要作用.AIM: To explore the effect of brain-derived neurotrophic factor(BDNF) on the proliferation and migration of ECa9706 cell line in vitro and the underlying mechanism. METHODS: Cell proliferation and migration were examined by MTT assay and transwell assay, respectively. The m RNA and protein expression levels of tyrosine kinase receptorB(Trk B) and phospholipase C(PLC)-γ1 were detected by real-time quantitative polymerase chain reaction(q PCR) and Western blot. RESULTS: BDNF enhanced the proliferation and migration of ECa9706 cells significantly in a dose-dependent manner, and this effect was blocked by K252a(a Trk B antagonist). Compared with control cells, BDNF increased the m RNA and protein expression of Trk B, and the protein expression of PLC-γ1.
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