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本文引用的文献

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Dysregulated expression of dicer and drosha in breast cancer.乳腺癌中 dicer 和 drosha 的表达失调。
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Common genetic polymorphisms of microRNA biogenesis pathway genes and risk of breast cancer: a case-control study in Korea.常见 miRNA 生物发生途径基因的遗传多态性与乳腺癌风险:韩国的病例对照研究。
Breast Cancer Res Treat. 2011 Dec;130(3):939-51. doi: 10.1007/s10549-011-1656-2. Epub 2011 Jul 16.
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Worldwide burden of cervical cancer in 2008.2008 年全球宫颈癌负担。
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Overexpression of Dicer predicts poor survival in colorectal cancer.Dicer 过表达预示结直肠癌患者预后不良。
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An essential role for Ran GTPase in epithelial ovarian cancer cell survival.Ran GTPase 在卵巢上皮性癌细胞存活中起关键作用。
Mol Cancer. 2010 Oct 13;9:272. doi: 10.1186/1476-4598-9-272.
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Association of a common AGO1 variant with lung cancer risk: a two-stage case-control study.AGO1 基因常见变异与肺癌风险的关联:一项两阶段病例对照研究。
Mol Carcinog. 2010 Oct;49(10):913-21. doi: 10.1002/mc.20672.
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Genetic variation in microRNA networks: the implications for cancer research.miRNA 网络中的遗传变异:对癌症研究的影响。
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The universal overexpression of a cancer testis antigen hiwi is associated with cancer angiogenesis.普遍过表达癌症睾丸抗原 hiwi 与癌症血管生成有关。
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Expression of HIWI in human esophageal squamous cell carcinoma is significantly associated with poorer prognosis.HIWI 在人食管鳞癌中的表达与更差的预后显著相关。
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Genetic variation in MicroRNA genes and risk of oral premalignant lesions.miRNA 基因遗传变异与口腔癌前病变风险
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中国人群中 miRNA 生物发生基因 RAN、DICER 和 HIWI 的遗传变异与宫颈癌风险。

Genetic variants in RAN, DICER and HIWI of microRNA biogenesis genes and risk of cervical carcinoma in a Chinese population.

机构信息

State Key Laboratory of Reproductive Medicine, Department of Epidemiology and Biostatistics, School of Public Health, Nanjing Medical University, Nanjing 210029, China; ; Section of Clinical Epidemiology, Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Cancer Center, Nanjing Medical University, Nanjing 210029, China;

出版信息

Chin J Cancer Res. 2013 Oct;25(5):565-71. doi: 10.3978/j.issn.1000-9604.2013.10.03.

DOI:10.3978/j.issn.1000-9604.2013.10.03
PMID:24255581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3828428/
Abstract

OBJECTIVE

Recent evidence indicates that dysregulation of microRNA (miRNA) biogenesis is implicated in cancer development and progression. Based on the important role of miRNA biogenesis genes in carcinogenesis, we hypothesized that genetic variations of the miRNA biogenesis genes may modulate susceptibility to cervical cancer.

METHODS

We identified three single nucleotide polymorphisms (SNPs) located in the 3'-untranslated regions (3'-UTR) of of miRNA biogenesis key genes (rs1057035 in DICER, rs3803012 in RAN and rs10773771 in HIWI) and genotyped these SNPs in a case-control study of 1,486 cervical cancer cases and 1,549 cancer-free controls in Chinese women.

RESULTS

Logistic regression analyses showed that no significant associations were observed between the three SNPs and cervical cancer risk [rs3803012 in RAN AG/GG vs. AA adjusted OR =1.104, 95% confidence interval (CI): 0.859-1.419; rs1057035 in DICER CT/CC vs. TT adjusted OR =0.962, 95% CI: 0.805-1.149; rs10773771 in HIWI CT/CC vs. TT adjusted OR =0.963, 95% CI: 0.826-1.122].

CONCLUSIONS

The findings did not suggest that genetic variants in the 3'-UTR of RAN, DICER and HIWI of miRNA biogenesis genes were associated with the risk of cervical cancer in this Chinese population.

摘要

目的

最近的证据表明,miRNA(miRNA)生物发生的失调与癌症的发生和发展有关。基于 miRNA 生物发生基因在致癌作用中的重要作用,我们假设 miRNA 生物发生基因的遗传变异可能调节宫颈癌的易感性。

方法

我们鉴定了位于 miRNA 生物发生关键基因 3'-非翻译区(3'-UTR)中的三个单核苷酸多态性(SNP)(DICER 中的 rs1057035、RAN 中的 rs3803012 和 HIWI 中的 rs10773771),并在一项中国女性宫颈癌病例对照研究中对这些 SNP 进行了基因分型。

结果

逻辑回归分析显示,三个 SNP 与宫颈癌风险之间没有显著关联[RAN 中的 rs3803012 AG/GG 与 AA 调整后的 OR=1.104,95%置信区间(CI):0.859-1.419;DICER 中的 rs1057035 CT/CC 与 TT 调整后的 OR=0.962,95% CI:0.805-1.149;HIWI 中的 rs10773771 CT/CC 与 TT 调整后的 OR=0.963,95% CI:0.826-1.122]。

结论

在该中国人群中,miRNA 生物发生基因 3'-UTR 中的遗传变异与宫颈癌风险无关。