Genes Correlated with Gemcitabine Efficacy in Non-small Cell Lung Cancer

Chunhong Li, Meiyan Liu, Hailing Lu, Wei Liu, L. Cai, Xiaoqun Dong
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引用次数: 1

Abstract

Objective: Gemcitabine in combination with platinum improves survival of patients with non-small cell lung cancer (NSCLC). The purpose of the study was to explore genes related to gemcitabine efficacy. Methods: The sensitivity of NSCLC cell lines to anticancer drugs was tested via MTT assay. Gene expression analysis was performed by cDNA microarray, and qRT-PCR was used for verification of the microarray results on highly sensitive genes. Fluorouracil (5-Fu) was used as the negative control of gemcitabine. Results: Gemcitabine-related and fluorouracil-related genes were pooled into different clusters. Genes negatively related to 5-Fu sensitivity were positively related to gemcitabine efficacy. Metallothionein, Cathepsin B, TIMP1 and Galectin-1 genes which were resisted to certain anticancer drugs were sensitive to gemcitabine (P<0.05). Conclusion: Metallothionein, Cathepsin B, TIMP1 and Galectin-1 can be considered as the predictors for gemcitabine sensitivity.
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与吉西他滨治疗非小细胞肺癌疗效相关的基因
目的:吉西他滨联合铂可提高非小细胞肺癌(NSCLC)患者的生存率。该研究的目的是探索与吉西他滨疗效相关的基因。方法:采用MTT法检测非小细胞肺癌细胞株对抗癌药物的敏感性。基因表达分析采用cDNA芯片,高敏感基因采用qRT-PCR对芯片结果进行验证。以氟尿嘧啶(5-Fu)作为吉西他滨阴性对照。结果:吉西他滨相关基因和氟尿嘧啶相关基因汇集成不同的簇。与5-Fu敏感性负相关的基因与吉西他滨疗效正相关。对部分抗癌药物耐药的金属硫蛋白、组织蛋白酶B、TIMP1、半凝集素-1基因对吉西他滨敏感(P<0.05)。结论:金属硫蛋白、组织蛋白酶B、TIMP1和半凝集素-1可作为吉西他滨敏感性的预测因子。
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