Suppr超能文献

实时定量聚合酶链反应配对设计研究:miR - 378*和miR - 145是人类结直肠癌有效的早期诊断生物标志物。

Paired design study by real-time PCR: miR-378* and miR-145 are potent early diagnostic biomarkers of human colorectal cancer.

作者信息

Peng Juan, Xie Zhengyong, Cheng Liyang, Zhang Yuxin, Chen Junyong, Yu Hongping, Li Zehang, Kang Huixing

机构信息

Guilin Medical College, Huang Cheng North 2 Road 109, Qixing District, Guilin, Guangxi, China.

General Hospital of Guangzhou Military Command of PLA, Liuhua Road 111, Guangzhou, Guangdong, China.

出版信息

BMC Cancer. 2015 Mar 21;15:158. doi: 10.1186/s12885-015-1123-2.

Abstract

BACKGROUND

Although microRNAs offer great potential as cancer biomarkers, effective clinical dignostics and tumor maker have not been verified to diagnose with colorectal cancer (CRC). The purpose of our study is to systematically assess the expression of miRNAs in matched cancer and normal tissue samples to identify promising diagnostic microRNA (miRNA) biomarkers for CRC.

METHODS

In our study, we examined by Real-Time PCR the expression levels of 96 mature miRNA in 32 CRC patients with differently expressed tumors versus normal colon tissues. Using enter and stepwise variable selection methods separately, conditional logistic regression was conducted to identify miRNAs associated with CRC. The classification performance of these indicators was assessed under the Fisher discriminant analysis. Receiver operating characteristic curve analyses were applied to obtain diagnostic utility of the differentially expressed miRNAs.

RESULTS

In this study, we confirmed 11 overexpressed miRNAs with no less than twofold difference, and 85 downexpressed miRNAs with up to 0.5-fold difference in CRC from 96 aberrantly expressed miRNAs being identified by real-time PCR. Conditional logistic regression results confirmed that miRNA-378 and miRNA-145 expression profile was statistically significant. The error diagnosis rate of these two miRNAs are 0.194 and 0.113, separeately, showing by discriminant analysis.

CONCLUSIONS

MiRNA-145 and miRNA-378* are potential biomarkers for early detection of CRC, which may help in diagnosing CRC in early period.

摘要

背景

尽管微小RNA作为癌症生物标志物具有巨大潜力,但有效的临床诊断和肿瘤标志物尚未被证实可用于诊断结直肠癌(CRC)。我们研究的目的是系统评估微小RNA在配对的癌组织和正常组织样本中的表达,以确定有前景的结直肠癌诊断性微小RNA(miRNA)生物标志物。

方法

在我们的研究中,我们通过实时荧光定量PCR检测了32例结直肠癌患者中96种成熟miRNA在肿瘤组织与正常结肠组织中差异表达的水平。分别使用逐步进入法和逐步变量选择法,进行条件逻辑回归以识别与结直肠癌相关的miRNA。在Fisher判别分析下评估这些指标的分类性能。应用受试者工作特征曲线分析来获得差异表达miRNA的诊断效用。

结果

在本研究中,通过实时荧光定量PCR从96种异常表达的miRNA中,我们确认了11种在结直肠癌中过表达且差异倍数不低于2倍的miRNA,以及85种下调且差异倍数高达0.5倍的miRNA。条件逻辑回归结果证实miRNA-378和miRNA-145的表达谱具有统计学意义。判别分析显示,这两种miRNA的错误诊断率分别为0.194和0.113。

结论

MiRNA-145和miRNA-378*是结直肠癌早期检测的潜在生物标志物,可能有助于早期诊断结直肠癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e533/4436811/84832c77a9ca/12885_2015_1123_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验