文章摘要

奥曲肽诱导人结肠癌细胞凋亡与细胞周期的影响及机制

作者: 1龙建武, 2梁庆模, 1周筱筠, 1李晶, 1刘龙飞, 1肖帅, 1卢先州
1 南华大学附属南华医院 普通外科,湖南 衡阳 421002
2 南华大学附属南华医院 肿瘤外科,湖南 衡阳 421002
通讯: 卢先州 Email: 158452871@qq.com
DOI: 10.3978/.10.3978/j.issn.1005-6947.2015.04.014
基金: 湖南省自然科学基金省市联合资助项目, 12JJ9030

摘要

目的:探讨奥曲肽诱导人结肠癌细胞凋亡与细胞周期的影响及机制。 方法:奥曲肽、GSK-3β 抑制剂LiCl 单独或联合作用于人结肠癌SW480 细胞后,用流式细胞术检测 SW480 细胞的凋亡与细胞周期,以及用DNA 凝胶电泳实验进一步验证细胞凋亡;Western blot 检测 SW480 细胞中GSK-3β、p-GSK3-β(Tyr216)及p-GSK-3β(Ser9)蛋白表达。 结果:与未处理的空白对照组SW480 比较,奥曲肽处理SW480 细胞后,细胞凋亡率与G0/G1 细胞明显 升高,凝胶电泳出现典型的“梯形”DNA 条带,总GSK-3β 蛋白与p-GSK3β(Tyr216)表达明显上调, 而p-GSK3β(Ser9)蛋白表达明显下降(均P<0.05);LiCl 单独作用对SW480 细胞的凋亡与细胞周 期无明显影响(均P>0.05),但与奥曲肽联合作用能明显削弱奥曲肽对SW480 的促凋亡与细胞周期阻 滞作用(均P<0.05)。 结论:奥曲肽能有效诱导SW480 细胞凋亡与细胞周期阻滞,该作用可能与其上调GSK-3β 蛋白的表达, 并调节GSK-3β 蛋白的磷酸化水平有关。
关键词: 结肠肿瘤 奥曲肽 糖原合成酶激酶3

Influence of octreotide on apoptosis and cell cycle in human colon cancer cells and the mechanism

Authors: 1LONG Jianwu, 2LIANG Qingmo, 1ZHOU Xiaojun, 1LI JING, 1LIU Longfei, 1XIAO Shuai, 1LU Xianzhou
1 Department of General Surgery, Affiliated NanHua Hospital, University of South China, Hengyang, Hunan 421002, China
2 Department of Surgical Oncology, Affiliated NanHua Hospital, University of South China, Hengyang, Hunan 421002, China

CorrespondingAuthor:LU Xianzhou Email: 158452871@qq.com

Abstract

Objective: To investigate the influence of octreotide on apoptosis and cell cycle in human colon cancer cells and the mechanism. Methods: Human colon cancer SW480 cells were exposed to octreotide or GSK-3β inhibitor LiCl alone or in combination; the apoptosis and cell cycle in SW480 were analyzed by flow cytometry, and the apoptosis was also verified by DNA agarose gel electrophoresis. In addition, the expressions of GSK-3β, p-GSK3β (Tyr216) and p-GSK3β (Ser9) in SW480 cells were determined by Western blot analysis. Results: Compared with the blank control group of untreated SW480 cells, in SW480 cells after octreotide treatment, the apoptosis and ratio of G0/G1 phase cells were significantly increased, typical DNA ladders were present in the agarose gel electrophoresis, and the total GSK-3β protein and p-GSK3β (Tyr216) protein expressions were significantly increased, while the p-GSK3β (Ser9) protein expression was significantly decreased (all P<0.05); LiCl treatment alone exerted no influence on apoptosis and cell cycle in SW480 cells (both P>0.05), but it significantly weakened the apoptosis-inducing and cell cycle arrest effect of octreotide in SW480 cells in combination with octreotide (both P<0.05). Conclusion: Octreotide can effectively induce apoptosis and cell cycle arrest in SW480 cells, which may be related to its increasing GSK-3β protein expression and regulating phosphorylation level of GSK-3β.
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