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miR-218-LAMB3 通路相关多态性与宫颈癌易感性的病例对照研究:中国女性。

Polymorphisms involved in the miR-218-LAMB3 pathway and susceptibility of cervical cancer, a case-control study in Chinese women.

机构信息

Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 210029, China.

出版信息

Gynecol Oncol. 2010 May;117(2):287-90. doi: 10.1016/j.ygyno.2010.01.020. Epub 2010 Feb 16.

DOI:10.1016/j.ygyno.2010.01.020
PMID:20163849
Abstract

OBJECTIVE

Laminin-5 is required in RAS and NF-kappaB blockade induced tumorigenesis of human squamous cell carcinoma and a marker of invasiveness in cervical lesions. MicroRNA-218 (miR-218) can target laminin-5 beta3 (LAMB3), but suppressed by HPV-16 E6 protein. Therefore, we hypothesized that single nucleotide polymorphisms (SNPs) in pri-miR-218 and LAMB3 may individually and/or jointly contribute to cervical cancer carcinogenesis.

METHODS

We identified one SNP rs11134527 located in pri-miR-218 sequence and one SNP rs2566 in 3'UTR of LAMB3 and genotyped these two SNPs in a case-control study of 703 cervical cancer cases and 713 cancer-free controls in Chinese women.

RESULTS

Logistic regression analyses showed that the pri-miR-218 rs11134527 variant homozygote GG was associated with a decreased risk of cervical cancer compared with the AA genotype (adjusted OR=0.72, 95% CI=0.52-0.99), while the LAMB3 rs2566 variant CT/TT genotypes were associated with a significantly increased risk of cervical cancer (adjusted OR=1.57, 95% CI=1.25-1.96), compared with the wild type CC genotype. A significant dose-response effect was observed between the number of risk alleles, rs11134527A and rs2566 T, and the risk of cervical cancer (P for trend=0.0006).

CONCLUSION

These findings indicate that pri-miR-218 rs11134527 and LAMB3 rs2566 may contribute to cervical cancer carcinogenesis, and further validations in diverse populations and functional characterizations are warranted.

摘要

目的

层粘连蛋白-5 是 RAS 和 NF-κB 阻断诱导的人鳞状细胞癌发生和宫颈病变侵袭性的标志物。微小 RNA-218(miR-218)可以靶向层粘连蛋白-5β3(LAMB3),但被 HPV-16 E6 蛋白抑制。因此,我们假设 pri-miR-218 和 LAMB3 中的单核苷酸多态性(SNP)可能单独和/或共同导致宫颈癌的发生。

方法

我们鉴定了位于 pri-miR-218 序列中的一个 SNP rs11134527 和 LAMB3 的 3'UTR 中的一个 SNP rs2566,并在中国女性的宫颈癌病例对照研究中对这两个 SNP 进行了基因分型,共纳入了 703 例宫颈癌病例和 713 例无癌对照。

结果

Logistic 回归分析表明,与 AA 基因型相比,pri-miR-218 rs11134527 变异纯合子 GG 与宫颈癌风险降低相关(调整后的 OR=0.72,95%CI=0.52-0.99),而 LAMB3 rs2566 变异 CT/TT 基因型与宫颈癌风险显著增加相关(调整后的 OR=1.57,95%CI=1.25-1.96),与野生型 CC 基因型相比。rs11134527A 和 rs2566T 的风险等位基因数量与宫颈癌风险之间存在显著的剂量反应关系(趋势检验 P=0.0006)。

结论

这些发现表明,pri-miR-218 rs11134527 和 LAMB3 rs2566 可能有助于宫颈癌的发生,需要在不同人群中进一步验证和功能特征分析。

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