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健康供体和前列腺肿瘤患者游离DNA中GSTP1、RNF219和KIAA1539基因位点特异性甲基化的单分子分辨率研究:在诊断中的应用

Locus-Specific Methylation of GSTP1, RNF219, and KIAA1539 Genes with Single Molecule Resolution in Cell-Free DNA from Healthy Donors and Prostate Tumor Patients: Application in Diagnostics.

作者信息

Bryzgunova Olga, Bondar Anna, Ruzankin Pavel, Laktionov Petr, Tarasenko Anton, Kurilshikov Alexander, Epifanov Rostislav, Zaripov Marat, Kabilov Marsel, Laktionov Pavel

机构信息

Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia.

Sobolev Institute of Mathematics, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia.

出版信息

Cancers (Basel). 2021 Dec 12;13(24):6234. doi: 10.3390/cancers13246234.

Abstract

The locus-specific methylation of three genes (GSTP1, RNF219, and KIAA1539 (also known as FAM214B)) in the blood plasma cell-free DNA (cfDNA) of 20 patients with prostate cancer (PCa), 18 healthy donors (HDs), and 17 patients with benign prostatic hyperplasia (BPH) was studied via the MiSeq platform. The methylation status of two CpGs within the same loci were used as the diagnostic feature for discriminating the patient groups. Many variables had good diagnostic characteristics, e.g., each of the variables GSTP1.C3.C9, GSTP1.C9, and GSTP1.C9.T17 demonstrated an 80% sensitivity at a 100% specificity for PCa patients vs. the others comparison. The analysis of RNF219 gene loci methylation allowed discriminating BPH patients with absolute sensitivity and specificity. The data on the methylation of the genes GSTP1 and RNF219 allowed discriminating PCa patients, as well as HDs, with absolute sensitivity and specificity. Thus, the data on the locus-specific methylation of cfDNA (with single-molecule resolution) combined with a diagnostic approach considering the simultaneous methylation of several CpGs in one locus enabled the discrimination of HD, BPH, and PCa patients.

摘要

通过MiSeq平台研究了20例前列腺癌(PCa)患者、18例健康供体(HDs)和17例良性前列腺增生(BPH)患者血浆游离DNA(cfDNA)中三个基因(GSTP1、RNF219和KIAA1539,也称为FAM214B)的位点特异性甲基化。同一基因座内两个CpG的甲基化状态被用作区分患者组的诊断特征。许多变量具有良好的诊断特性,例如,变量GSTP1.C3.C9、GSTP1.C9和GSTP1.C9.T17中的每一个在PCa患者与其他组的比较中,在100%特异性时均表现出80%的敏感性。对RNF219基因座甲基化的分析能够以绝对的敏感性和特异性区分BPH患者。关于GSTP1和RNF219基因甲基化的数据能够以绝对的敏感性和特异性区分PCa患者以及HDs。因此,cfDNA位点特异性甲基化(具有单分子分辨率)的数据与考虑一个基因座中多个CpG同时甲基化的诊断方法相结合,能够区分HD、BPH和PCa患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec3f/8699300/3d662c9f6f67/cancers-13-06234-g001.jpg

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