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Mol Clin Oncol. 2017 Dec;7(6):1152-1158. doi: 10.3892/mco.2017.1462. Epub 2017 Oct 18.

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1
miRNAs associated with prostate cancer risk and progression.与前列腺癌风险和进展相关的微小RNA
BMC Urol. 2017 Mar 20;17(1):18. doi: 10.1186/s12894-017-0206-6.
2
MiR-1, a Potential Predictive Biomarker for Recurrence in Prostate Cancer After Radical Prostatectomy.MiR-1,一种前列腺癌根治术后复发的潜在预测生物标志物。
Am J Med Sci. 2017 Apr;353(4):315-319. doi: 10.1016/j.amjms.2017.01.006. Epub 2017 Jan 31.
3
miR-1307 promotes the proliferation of prostate cancer by targeting FOXO3A.miR-1307 通过靶向 FOXO3A 促进前列腺癌的增殖。
Biomed Pharmacother. 2017 Apr;88:430-435. doi: 10.1016/j.biopha.2016.11.120. Epub 2017 Jan 22.
4
Exosomal microRNAs in liquid biopsies: future biomarkers for prostate cancer.液体活检中的外泌体微小RNA:前列腺癌的未来生物标志物
Clin Transl Oncol. 2017 Jun;19(6):651-657. doi: 10.1007/s12094-016-1599-5. Epub 2017 Jan 4.
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An indel polymorphism within pre-miR3131 confers risk for hepatocellular carcinoma.
Carcinogenesis. 2017 Feb 1;38(2):168-176. doi: 10.1093/carcin/bgw206.
6
Pri-miR-34b/c rs4938723 polymorphism increased the risk of prostate cancer.微小RNA前体-34b/c rs4938723多态性增加了前列腺癌的发病风险。
Cancer Biomark. 2017;18(2):155-159. doi: 10.3233/CBM-160058.
7
Recent scenario of microRNA as diagnostic and prognostic biomarkers of prostate cancer.微小RNA作为前列腺癌诊断和预后生物标志物的最新情况。
Urol Oncol. 2017 Mar;35(3):92-101. doi: 10.1016/j.urolonc.2016.10.019. Epub 2016 Nov 24.
8
Pri-miR-34b/c rs4938723 polymorphism is associated with the risk of childhood acute lymphoblastic leukemia.微小RNA前体-34b/c rs4938723多态性与儿童急性淋巴细胞白血病风险相关。
Cancer Genet. 2016 Nov;209(11):493-496. doi: 10.1016/j.cancergen.2016.09.009. Epub 2016 Sep 30.
9
Effect of rs11614913 Polymorphism on Mature miR196a2 Expression and its Target Gene HOXC8 Expression in Human Glioma.rs11614913多态性对人胶质瘤中成熟miR196a2表达及其靶基因HOXC8表达的影响
J Mol Neurosci. 2017 Feb;61(2):144-151. doi: 10.1007/s12031-016-0855-z. Epub 2016 Oct 28.
10
Association between microRNA-27a rs895819 polymorphism and risk of colorectal cancer: A meta-analysis.微小RNA-27a rs895819多态性与结直肠癌风险的关联:一项荟萃分析。
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运用错配聚合酶链反应-限制性片段长度多态性技术评估前列腺癌患者前体微小RNA-3131内一个3碱基对插入/缺失多态性

Evaluation of a 3-base pair indel polymorphism within pre-microRNA-3131 in patients with prostate cancer using mismatch polymerase chain reaction-restriction fragment length polymorphism.

作者信息

Hashemi Mohammad, Bahari Gholamreza, Sattarifard Hedieh, Narouie Behzad

机构信息

Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan 98167-43181, Iran.

Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan 98167-43181, Iran.

出版信息

Mol Clin Oncol. 2017 Oct;7(4):696-700. doi: 10.3892/mco.2017.1369. Epub 2017 Aug 8.

DOI:10.3892/mco.2017.1369
PMID:28856004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5574207/
Abstract

The present study aimed to examine the impact of a 3-bp indel (rs57408770) polymorphism within the pre-microRNA (miR)-3131 polymorphism on prostate cancer (PCa) risk in a sample of an Iranian population. In total, 340 subjects, including 177 patients with PCa and 170 patients with benign prostatic hyperplasia, were enrolled in the present case-control study. A mismatch polymerase chain reaction-restriction fragment length polymorphism method was designed for genotyping the 3-bp indel (rs57408770) polymorphism. The present findings demonstrated that the indel variant significantly increased the risk of PCa in codominant [odds ratio (OR)=2.23, 95% confidence interval (CI)=1.13-4.37; P=0.021, insertion (ins)/ins vs. deletion (del)/del] and recessive (OR=2.33, 95% CI=1.25-4.36; P=0.009, ins/ins vs. del/del + del/ins). In conclusion, to the best of our knowledge, the present findings for the first time proposed that a 3-bp indel variant of miR-3131 may be a risk factor for susceptibility to PCa in a sample of an Iranian population. Further studies with different ethnicities and larger sample sizes are required to validate the present findings.

摘要

本研究旨在检测前体微小RNA(miR)-3131的3个碱基对插入缺失(rs57408770)多态性对伊朗人群样本中前列腺癌(PCa)风险的影响。本病例对照研究共纳入340名受试者,包括177例PCa患者和170例良性前列腺增生患者。设计了错配聚合酶链反应-限制性片段长度多态性方法对3个碱基对插入缺失(rs57408770)多态性进行基因分型。本研究结果表明,该插入缺失变异在共显性模型中[比值比(OR)=2.23,95%置信区间(CI)=1.13 - 4.37;P = 0.021,插入(ins)/ins与缺失(del)/del相比]和隐性模型中(OR = 2.33,95% CI = 1.25 - 4.36;P = 0.009,ins/ins与del/del + del/ins相比)均显著增加PCa风险。总之,据我们所知,本研究结果首次提出miR-3131的3个碱基对插入缺失变异可能是伊朗人群样本中PCa易感性的一个风险因素。需要开展不同种族和更大样本量的进一步研究来验证本研究结果。