上海口腔医学 ›› 2015, Vol. 24 ›› Issue (1): 30-36.

• 基础研究 • 上一篇    下一篇

氯喹增强口腔癌CAL-27细胞对顺铂化疗敏感性的观察

全海英1,2,周丽佳1,李昂迪1,张泽兵1   

  1. 1.吉林大学口腔医院 病理科,吉林 长春 130021;
    2.吉林医药学院附属医院 口腔科,吉林 吉林 132013
  • 收稿日期:2014-02-17 出版日期:2015-02-20 发布日期:2015-07-24
  • 通讯作者: 张泽兵,Tel:0431-85579328,E-mail:zebing@jlu.edu.cn
  • 作者简介:全海英(1987-),女,硕士研究生,医师,E-mail:hanbingsui111@163.com
  • 基金资助:
    吉林省科技厅基金(201105101); 吉林省卫生厅基金(20132004)

Mechanism of chloroquine in promoting sensitivity of chemotherapeutics in oral squamous cell carcinoma CAL-27 cell line to cisplatin

QUAN Hai-ying1,2,ZHOU Li-jia1,LI Ang-di1,Zhang Ze-bing1   

  1. 1.Department of Pathology, Stomatological Hospital, Jilin University. Changchun 130021;
    2.Department of Stomatology, the Affiliated Hospital of Jilin Medical College. Jilin 132013, Jilin Province, China
  • Received:2014-02-17 Online:2015-02-20 Published:2015-07-24
  • Supported by:
    Research Fund of Department of Science and Technology of Jilin Province (20115101) and Department of Health of Jilin Province (20132004)

摘要: 目的利用氯喹(chloroquine,CQ)及顺铂(cisplatin,DDP)作用于CAL-27细胞,探讨自噬在口腔癌化疗中的作用及机制,为临床增强口腔癌化疗敏感性提供理论依据。方法应用四甲基偶氮唑蓝(MTT)比色法比较药物对CAL-27细胞的生长抑制作用,采用激光共聚焦显微镜观察自噬特异性蛋白LC3-Ⅱ的表达,AnnexinV/PI双染色流式细胞仪检测细胞凋亡,流式细胞术观察细胞周期的分布。采用SPSS17.0软件包对数据进行统计学分析。结果不同浓度氯喹及顺铂处理CAL-27细胞不同时间后,细胞生存率逐渐降低,呈浓度和时间依赖性。5 mg/L氯喹联合顺铂在IC50浓度(5 mg/L)处理后,与单独顺铂处理相比,显著降低了CAL-27细胞的生存率(P<0.05)。氯喹或顺铂作用于CAL-27细胞48 h后,自噬在细胞中分布清晰,顺铂组(DDP组)细胞平均荧光强度高于对照组、氯喹处理组(CQ组)及氯喹与顺铂联合处理组(CQ+DDP组)(P<0.05);氯喹组细胞平均荧光强度显著低于其他3组(P<0.05)。氯喹或顺铂作用于CAL-27细胞48 h后,与对照组相比,DDP组和CQ+DDP组细胞凋亡率显著提高(P<0.05);与顺铂单独作用相比,CQ+DDP组细胞凋亡率显著提高(P<0.05)。氯喹和顺铂作用于CAL-27细胞48 h后,DDP组和CQ+DDP组G1期细胞明显增多,出现G1期阻滞,CQ+DDP组G1期细胞数显著高于DDP组(P<0.05)。结论抑制自噬能够提高CAL-27细胞对顺铂的化疗敏感性,CAL-27细胞本身的自噬是产生化疗耐药的重要机制。自噬抑制剂有望成为口腔癌化疗的增敏剂。

关键词: 细胞自噬, 顺铂, 氯喹, 细胞凋亡, 口腔鳞状细胞癌

Abstract: PURPOSE: To study the role and mechanism of autophagy in chemotherapy of oral squamous cell carcinoma, and provide theoretical evidence to improve chemotherapeutic efficacy of oral squamous cell carcinoma patients. METHODS: The cell survival rate changes induced by cisplatin (DDP) and chloroquine (CQ) in CAL-27 cells were assayed by methyl thiazolyl tetrazolium method(MTT). The LC3-Ⅱ expression level was detected by laser scanning confocal microscope; The apoptotic rate was determined by flow cytometry. SPSS17.0 software package was used for statistical analysis. RESULTS: MTT results showed that compared with the control group, the cell survival rate reduced with the increasing time of DDP and CQ treatment; The optimal concentration of CAL-27 cells was 5 mg/L after treatment with CQ. IC50 of the CAL-27 cells was 5 mg/L after treatment with DDP; MTT results showed that the cell survival rate of CQ+DDP group was significantly lower than control group, CQ group and DDP group (P<0.05). With the action of CQ and DDP to CAL-27 cells for 48 hours, immunofluorescence results showed that the average fluorescence intensity of DDP group was significantly higher than the other 3 groups (P<0.05), while it was significantly lower in CQ group than the other 3 groups (P<0.05). With the action of CQ and DDP to CAL-27 cells for 48 hours, flow cytometry results showed that the cell apoptosis rate of DDP group and CQ+DDP group were significantly higher than control group and CQ group. The cell apoptosis rate of CQ+DDP group was significantly higher than DDP group (P<0.05). With the action of CQ and DDP to CAL-27 cells for 48 hours, cells in G1 phase of DDP group and CQ+DDP group increased, indicating G1 phase blockage. The cell count in G1 phase of CQ+DDP group was significantly higher than DDP group (P<0.05). CONCLUSIONS: Inhibition of autophagy can enhance the chemotherapeutic sensitivity of DDP in CAL-27 cells. Autophagy in CAL-27 cells is an important mechanism for chemotherapy resistance of oral squamous cell carcinoma. Autophagy inhibitor may have significant potential to be a novel chemotherapeutic sensitizer for oral squamous cell carcinoma.

Key words: Cell autophagy, Cisplatin, Chloroquine, Cell apoptosis, Oral squamous cell carcinoma

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