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作 者:樊晓妹[1] 李魁秀[1] 李琰[2] 房朝辉[1] 牛书怀[1] 金鸽[1]
机构地区:[1]河北医科大学第四医院,河北石家庄050000 [2]河北省肿瘤研究所,河北石家庄050000
出 处:《实用妇产科杂志》2014年第1期33-36,共4页Journal of Practical Obstetrics and Gynecology
摘 要:目的:探讨表皮生长因子受体(EGFR)基因R497K及.216G/T单核苷酸多态性(SNP)与宫颈癌患者放化疗近期疗效的关系。方法:应用聚合酶链反应一连接酶检测反应方法,检测了196例接受单纯放疗或放疗合并化疗的宫颈癌的EGFR基因R497K、-216G/T两个SNP。结果:与携带R497KG/G基因型组相比,携带A/A基因型组放疗敏感性差异有统计学意义(P〈0.05),校正OR值为0.244(95%C10.087~0.680);与携带-216G/G基因型组相比,携带G/T+T/T基因型组放疗敏感性差异无统计学意义,校正OR值为2.412(95%C10.856—6.797)。与携带R497KG/G基因型相比,携带A/A基因型组复发转移风险差异有统计学意义(P〈0.05),校正OR值为0.248(95%C10.078~0.786);与携带-216G/G基因型的患者相比,携带G/T4-T/T基因型组复发转移风险差异无统计学意义(P〉0.05),校正OR值为1.027(95%C10.324~3.253)。结论:EGFR基因R497K多态性位点与宫颈癌患者放化疗近期疗效及复发或转移风险相关,可能是预测宫颈癌放疗近期疗效及复发或转移的预测指标。Objective:This study was designed to investigate the association of EGFR R497K and -216G/ T single nucleotide polymorphisms with radiochemotherapy response in cervical cancer. Methods :The geno- type of EGFR R497K and -216G/T were analyzed by polymerase chain reaction-ligation detection reaction (PCR-LDR) in 196 cervical cancer patients whounderwent radiotherapy alone or radiotherapy combined with chemotherapy. Results:Compared with patients with R497K G/G genotype,the patients with A/A genotype had a significantly higher sensitivity to radiochemotherapy treatment (adjusted OR = 0. 244,95% CI 0. 087 ~ 0. 680). Compared with the patients with -216G/G genotype,the patients with G/T + T/T genotypes had no significant difference in sensitivity to radiochemotherapy( adjusted OR =2.412,95% CI 0. 856 -6. 979 ). Com- pared with the patients with R497K G/G genotype,the patients with A/A genotype had a decreased risk of recurrencemetastasis ( adjusted OR = 0. 248,95% CI 0. 078 ~ 0. 786, P 〈 0. 05). Compared with the paitents with -216G/G genotype, the patients with G/T + T/T genotypes had no significant difference in the risk of re- currence/metastasis(adjusted OR = 1. 027,95% CI 0. 324 -3. 253). Conclusions: In our study, the R497K polymorphisms have a relationship with treatment response and the risk of recurrencemetastasis for cervical cancer. R497K SNP might be a genetic marker for prediction radiochemotherapy response and the risk of re- currence/metastasis of patients with cervical cancer.
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