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O-6-甲基鸟嘌呤-DNA甲基转移酶基因启动子甲基化与肺癌风险:一项荟萃分析。

O-6-methylguanine-DNA methyltransferase gene promoter methylation and lung cancer risk: A meta-analysis.

作者信息

Yang Zhijia, Li Fangjun

机构信息

Department of Emergency, Huaihe Hospital of Henan University, Henan Kaifeng 475000, PR China.

出版信息

J Cancer Res Ther. 2016 Dec;12(Supplement):C233-C236. doi: 10.4103/0973-1482.200745.

Abstract

OBJECTIVE

To evaluate O-6-methylguanine-DNA methyltransferase (MGMT) gene promoter methylation pattern in tumor tissue and autologous controls (plasma, normal lung tissue, and bronchial lavage fluid [BLF]) in patients with nonsmall cell lung cancer (NSCLC).

MATERIALS AND METHODS

We electronic searched the MEDLINE and CNKI databases to find the open published studies related to MGMT gene promoter hypermethylation in NSCLC patients. The odds ratio (OR) for hypermethylation in plasma, BLF, and tissue was pooled by fixed or random effect model according to the statistical heterogeneity across the included studies.

RESULTS

After searching the related databases, we finally included 13 studies in this meta-analysis. The hypermethylation rate of tumor tissue, plasma, BLF, and control tissue of MGMT gene in NSCLC patients were 0.34 ± 0.20, 0.18 ± 0.14, and 0.39 ± 0.23; the statistical heterogeneity across the studies was evaluated by Chi-square and I2-test. Moreover, no statistical heterogeneity was existed in the aspects of hypermethylation for plasma, BLF, and tissue (P < 0.05). Meta-analysis showed the hypermethylation rate in tumor tissue was significantly higher than normal lung tissue (OR = 4.18, 95% CI: 2.76-6.32) and plasma (OR = 2.37, 95% CI: 1.49-3.75) in NSCLC patients. However, for BLF (OR = 2.05, 95% CI: 0.88-4.78), the hypermethylation rate was not statistical different (P > 0.05).

CONCLUSION

Hypermethylation rate in MGMT gene promoter of cancer tissue was statistical higher than autologous controls which indicated that MGMT may play an important in the cancer development.

摘要

目的

评估非小细胞肺癌(NSCLC)患者肿瘤组织及自体对照(血浆、正常肺组织和支气管灌洗液[BLF])中O-6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)基因启动子甲基化模式。

材料与方法

我们通过电子检索MEDLINE和CNKI数据库,查找与NSCLC患者MGMT基因启动子高甲基化相关的公开研究。根据纳入研究的统计异质性,采用固定效应或随机效应模型汇总血浆、BLF和组织中高甲基化的比值比(OR)。

结果

检索相关数据库后,我们最终纳入了13项研究进行该荟萃分析。NSCLC患者MGMT基因的肿瘤组织、血浆、BLF和对照组织的高甲基化率分别为0.34±0.20、0.18±0.14和0.39±0.23;采用卡方检验和I²检验评估研究间的统计异质性。此外,血浆、BLF和组织高甲基化方面不存在统计异质性(P<0.05)。荟萃分析显示,NSCLC患者肿瘤组织中的高甲基化率显著高于正常肺组织(OR=4.18,95%CI:2.76-6.32)和血浆(OR=2.37,95%CI:1.49-3.75)。然而,对于BLF(OR=2.05,95%CI:0.88-4.78),高甲基化率无统计学差异(P>0.05)。

结论

癌组织中MGMT基因启动子的高甲基化率在统计学上高于自体对照,这表明MGMT可能在癌症发展中起重要作用。

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