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全血中循环的微小RNA-200家族是高级别浆液性上皮性卵巢癌的潜在生物标志物。

The circulating microRNA-200 family in whole blood are potential biomarkers for high-grade serous epithelial ovarian cancer.

作者信息

Pendlebury Adam, Hannan Natalie J, Binder Natalie, Beard Sally, Mcgauran Monica, Grant Peter, Tong Stephen, Whitehead Clare L

机构信息

Department of Gynaecological Oncology, University of Melbourne, Mercy Hospital for Women, Heidelberg, Vic 3084, Australia.

Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, Heidelberg, Vic 3084, Australia.

出版信息

Biomed Rep. 2017 Mar;6(3):319-322. doi: 10.3892/br.2017.847. Epub 2017 Jan 25.

DOI:10.3892/br.2017.847
PMID:28451393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5403187/
Abstract

Epithelial ovarian cancer (EOC) is the leading cause of mortality with regard to gynaecological cancer. There is no effective biomarker and therefore prognosis is poor as the majority of cases are not diagnosed until advanced disease is present. MicroRNAs (miRs) are dysregulated in ovarian cancer tissue and are present in the circulation. The aim of the present study was to investigate whether circulating miRs from the miR-200 family served as potential candidate biomarkers for the early detection of EOC. Whole blood and ovarian tissue were collected from women with early (stage I/II, n=4), advanced EOC (stage III/IV, n=4), and women with benign ovarian masses (n=5). A panel of 5 miRs were studied in whole blood and ovarian tissue using Taqman RT-PCR miR assays. The expression of circulating miR-200a, miR-200b and miR-200c were upregulated (P<0.05) in ovarian cancer compared to controls, correlated with the stage of disease and reflected tissue expression. Despite a trend, there was no significant increase in the expression of miR-21 and miR-210 in the present study. In conclusion, the circulating miR-200 family may be promising candidate biomarkers for EOC that require validation in a larger study.

摘要

上皮性卵巢癌(EOC)是妇科癌症死亡的主要原因。由于缺乏有效的生物标志物,且大多数病例直到疾病晚期才被诊断出来,因此其预后较差。微小RNA(miR)在卵巢癌组织中表达失调且存在于循环中。本研究的目的是调查来自miR-200家族的循环miR是否可作为EOC早期检测的潜在候选生物标志物。收集了早期(I/II期,n = 4)、晚期EOC(III/IV期,n = 4)女性患者以及患有良性卵巢肿块的女性(n = 5)的全血和卵巢组织。使用Taqman RT-PCR miR检测法在全血和卵巢组织中研究了一组5种miR。与对照组相比,卵巢癌患者循环miR-200a、miR-200b和miR-200c的表达上调(P<0.05),与疾病分期相关并反映组织表达情况。尽管有趋势,但本研究中miR-21和miR-210的表达没有显著增加。总之,循环miR-200家族可能是EOC有前景的候选生物标志物,但需要在更大规模的研究中进行验证。