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作 者:孙臻峰[1] 沈斌[1] 张佳[1] 苏甜甜[1] 董频[1]
机构地区:[1]上海市第一人民医院耳鼻咽喉头颈外科,上海200080
出 处:《临床耳鼻咽喉头颈外科杂志》2015年第11期1016-1019,共4页Journal of Clinical Otorhinolaryngology Head And Neck Surgery
摘 要:目的:探讨耐药基因MDR1(P-gp)和ABCG2在Hep-2细胞耐药中的作用。方法:应用流式细胞仪检测MDR1和ABCG2抑制剂对于Hep-2喉癌细胞株积聚和外排抗肿瘤药物功能的影响,以及MDR1和ABCG2抑制剂对于Hep-2喉癌细胞株增敏作用的影响。结果:ABCG2抑制剂FTC在Hep-2细胞对Mitoxantrone吸收、外排检测实验中与对照组比较,差异有统计学意义;P-gp在该实验中与对照组差异无统计学意义;当抗肿瘤药物为Mitoxantrone及Cisplatin时,P-gp及ABCG2拮抗剂的加入对Hep-2细胞活力检测与对照组比较,差异无统计学意义;当抗肿瘤药为Doxorubicin时,FTC、P-gp单独作用对Hep-2细胞活力影响与对照组比较差异无统计学意义;而当FTC+P-gp时,对Hep-2细胞活力影响与对照组比较差异有统计学意义(P<0.05);当抗肿瘤药为5-FU时,P-gp对Hep-2细胞活力影响相比对照组差异有统计学意义(P<0.05),而FTC对该药耐药几乎无任何影响,FTC+P-gp也无效;当抗肿瘤药为Paclitaxel时,P-gp对Hep-2细胞活力影响相比对照组差异有统计学意义,FTC+P-gp对Hep-2细胞活力影响相比对照组差异有统计学意义(P<0.05)。结论:ABCG2可能主要通过影响化疗药物在细胞中的积聚与外排导致细胞耐药。P-gp产生耐药的方式可能有其他途径。P-gp和ABCG2在不同的化疗药物耐药作用中扮演不同的角色。Objective:To study the effect of MDR1 (P-gp) and ABCG2 on the drug resistance in Hep 2 cells. Method:Flow cytometry was used to detect the variations of the antitumor drugs accumulation and discharging, and activity variations when MDR1 and ABCG2 inhibitors were used in Hep-2. Result: The accumulation and dis- charging of mitoxantrone was significantly higher than the control group when ABCG2 inhibitor FTC was used in Hep-2 (P〈0.05). In contrast, P-gp did not appear similar case; To the mitoxantrone and cisplatin, there was no statistical correlation about activity of Hep-2 between P-gp or ABCG2 antagonist and the control; To the doxorubicin, combining FTC and P-gp, the activity of Hep-2 was higher than the control and difference was significant (P〈0.05), In contrast, FTC and P-gp did not appear similar case when use/ alone; To the 5-FU, when PGP used, the activity of Hep-2 was higher than that in the control and difference was significant (P〈0.05), In con- trast, FTC and FTC+P-gp did not appear similar case; To the paelitaxel, wl-en P-gp or FTC+P-gp used, the activity of Hep-2 was higher than that in the control and difference was significant(P〈0.05). Conclusion: ABCG2 may lead to drug resistance mainly by changing the ability of cell in accumulating and discharging chemotherapy drugs. P-gp has other way. P-gp and ABCG2 play different roles in different drug resistance.
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