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论文摘要

X-性染色体连锁凋亡抑制蛋白与口腔鳞癌细胞Tca8113化疗耐药的关系

Expression of X-linked inhibitor of apoptosis protein in Tca8113 cell and its relationship to chemoresistance

作者:王家凤 张志民 王成坤 聂代邦 高文信

Author:WANG Jia-feng1, ZHANG Zhi-min1, WANG Cheng-kun1, NIE Dai-bang2, GAO Wen-xin1

收稿日期:2010-02-25          年卷(期)页码:2010,28(01):92-92-94

期刊名称:华西口腔医学杂志

Journal Name:West China Journal of Stomatology

关键字:口腔鳞状细胞癌,X-性染色体连锁凋亡抑制蛋白,化疗耐药,

Key words:oral squamous cell carcinoma,X-linked inhibitor of apoptosis protein,chemoresistance,

基金项目:

吉林省科技发展计划基金资助项目(20050405-1);吉林大学创新基金资助项目(419070200084)

中文摘要

目的研究X-性染色体连锁凋亡抑制蛋白(XIAP)在口腔鳞癌细胞Tca8113中的表达水平,并探讨XIAP表达与Tca8113细胞对化疗药物耐药性之间的关系。方法用平阳霉素(PYM)间歇性加药,逐步递增剂量,采用甲基噻唑基四唑(MTT)法检测药物处理前后细胞对PYM的敏感性,逆转录聚合酶链反应(RT-PCR)分别检测XIAP在药物处理前后的各Tca8113细胞组中的表达变化,并探讨XIAP与细胞耐药性的关系。结果Tca8113细胞在PYM间断作用下产生耐受,Tca8113-1-10组、Tca8113-10-10组耐药细胞对PYM的半数有效浓度(IC50)分别为(12.758±0.030)、(18.986±0.150)μg·mL-1。Tca8113-1-20、Tca8113-10-20组耐药细胞对PYM的IC50分别为(26.302±0.072)、(35.294±0.115)μg·mL-1。XAIP的表达水平与细胞对PYM的耐药有相关性(P

英文摘要

Objective To explore the expression of X-linked inhibitor of apoptosis protein(XIAP) in Tca8113 cell, and to investigate its relationship to the chemoresistance. Methods The Tca8113 cell line was cultured by IMDM and the concentration of Pingyangmycin(PYM) added to Tca8113 cell line was increased gradually and continually, which was to induce the PYM-resistance in Tca8113 cell line. The sensitivity of Tca8113 cell to PYM and expression of XIAP were measured with methyl thiazolyl tetrazolium(MTT) chromatometry and reverse transcriptionpolymerase chain raction(RT-PCR). The XIAP level in the cells and its chemoresistance to PYM were analyzed by linear regression. Results The IC50 of Tca8113-1-10 group and Tca8113-10-10 group were(12.758±0.030), (18.986± 0.150)μg·mL-1 respectively. The IC50 of Tca8113-1-20 group and Tca8113-10-20 group increased to(26.302±0.072), (35.294±0.115)μg·mL-1 respectively. There was a relation between XIAP and the drug-resistance in Tca8113 cell. Conclusion XIAP may play an important role in the chemoresistance which might serve as a new therapeutic target for oral squamous cell carcinoma.

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