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作 者:赵雪强[1] 蒋碧佳[1] 银建华[1] 唐碧芸 黄秀兰[1] 李文翠[1]
机构地区:[1]桂林医学院附属医院临桂分院呼吸内科,广西桂林541199
出 处:《现代肿瘤医学》2015年第10期1352-1355,共4页Journal of Modern Oncology
基 金:广西卫生厅立项课题项目(编号:Z2013490)
摘 要:目的:探讨肿瘤坏死因子相关凋亡诱导配体(tumor necrosis factor related apoptosis inducing ligand,TRAIL)联合三氧化二砷(arsenic trioxide,ATO)对裸鼠肺癌移植瘤的抗肿瘤作用及可能机制。方法:将裸鼠肺癌移植瘤模型随机分为生理盐水组、TRAIL组、ATO组及TRAIL+ATO组,称瘤重并计算抑瘤率,用RTPCR检测NF-κB、Caspase-3、Survivin基因表达变化。结果:与生理盐水组比较,ATO组对裸鼠肺癌移植瘤具有抑制作用,联合用药具有协同增效作用,抑制NF-κB表达,下调Survivin mRNA,上调Caspase-3的表达。结论:ATO可能通过NF-κB通路,下调Survivin,上调Caspase-3增强TRAIL对裸鼠肺癌移植瘤的抗肿瘤作用。Objective:To study the inhibitory action and mechanism of TRAIL combined with ATO on tansplanted human lung cancer in nude mice. Methods: Nude mice bearing A549 lung cancer were randomly divided into normal saline group, TRAIL group, ATO group and TRAIL + ATO group. Tumor tissues were weighted and inhibitory rate was observed. Nuclear factor kappa B ( NF - κB), Caspase - 3, Survivin mRNA were assayed by reverse transcriptase - polymerase chain reaction( RT -PCR). Results:Compared with NS, both ATO and ATO + TRAIL obviously inhibited the growth of tansplanted human lung cancer in nude mice. They had a synergistic effect (P 〈 0.05), down - regulated the expression of NF - KB and Survivin, up - regulated the expression of Caspase - 3 ( P 〈 0.05 ). Conclusion : ATO combining with TRAIL can synergistic inhibit the gowth of tansplanted human lung cancer in nude mice, possible mechanism may be inhibition of NF -κB signaling pathway and down - regulation of Survivin expression, up - regulation of Caspase - 3 expression.
关 键 词:三氧化二砷 肿瘤坏死因子相关凋亡诱导配体 肺肿瘤 NF-ΚB
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