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作 者:马骐[1] 孟令权[1] 刘景昌[1] 胡建平[1] 葛军[1] 万玉良[1] 姜杉[1]
机构地区:[1]中国石油中心医院普通外科,河北廊坊 065000
出 处:《中华医学杂志》2008年第10期716-718,共3页National Medical Journal of China
摘 要:目的探讨奥曲肽对人肝癌细胞抑制作用的机制,为奥曲肽临床应用提供实验依据。方法用奥曲肽4、7、10μg/ml作用人肝癌细胞株(SMMC-7721)24、48、72h,以空白作为对照组;采用原位末端标记(TUNEL)法流式细胞仪检测SMMC-7721凋亡;直接标记单克隆(CD95/CD178)抗体法流式细胞仪检测SMMC-7721Fas/FasL表达的变化。结果奥曲肽在4、7、10μg/ml作用SMMC-772124h后,SMMC-7721凋亡率从8%升高为40%(P〈0.05),Fas表达率从57%升高为76%(P〈0.05),FasL表达率从54%升高为63%(P〈0.05)。结论奥曲肽能诱导肝癌细胞(HepSMMC-7721)凋亡的发生,而且能促进肝癌细胞Fas/Fasl基因的表达。Objective To investigate the effects of octreotide on apoptosis of and Fas/FasL gene expression in human hepatoma cell mechanism of the suppression effect of liver cancer with e in order to offer the experimental foundation for clinic treatment. Methods Hyman hematoma cells of the line SMMC-7721 were cultured and divided into two groups: octreotide group, co-cultured with octreotide 4,7, and 10 μg/ml respectively for 24 h, 48 h, or 72 h, and control group. TUNEL was used to detect the apoptosis of the cells. Flow cytometry was used with terminal deoxynucleatidyl transferase mediated dUTP nick end labeling (TUNEL) technique to detect the apoptosis of the cells. FC was used with direct labeling of monoclonal antibody ( CD95/CD178 ) to detect the expression of Fas and FasL, and the Fas/FasL ratio. Results Octreotide increased the apoptotic rate of the cells dose- and time-dependently ( all P 〈 0.05 ). Octreotide increased the Fas expression rate, FasL expression rate, and Fas/FasL ratio dose- and time-dependently ( all P 〈 0. 05 ). Conclusion Octreotide induces the apoptosis of human hepatoma cells, possibly by the mechanism of facilitating the Fas/FasL gene expression.
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