Combination of miR-125b and miR-27a enhances sensitivity and specificity of AFP-based diagnosis of hepatocellular carcinoma
Combination of miR-125b and miR-27a enhances sensitivity and specificity of AFP-based diagnosis of hepatocellular carcinoma
复制标题
miR-125b 和 miR-27a 的组合增强基于 AFP 的肝细胞癌诊断的敏感性和特异性
DOI:
10.1007/s13277-015-4545-1
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发表时间:
2016-05
期刊:
影响因子:
--
通讯作者:
Guo Hua
中科院分区:
文献类型:
--
作者:
Xi Qing;Luo Yi;Zhang Ning;Guo Hua
Non-invasive biomarkers of early-stage hepatocellular carcinoma (HCC) could offer immense benefits. Currently available tumor markers for HCC are of not much clinical relevance. In this study, we investigated the potential for using a panel of serum microRNAs (miRNAs) as novel tumor markers in conjunction with serum alpha-fetoprotein (AFP) for diagnosis of HCC. Serum expression of four miRNAs was assessed in 150 subjects (90 cases of HCC and 60 cases without cancer) by quantitative real-time polymerase chain reaction (qRT-PCR). Logistic regression analysis was performed to assess the potential use of miRNAs for detection of HCC. Receiver operating characteristic curves were used to evaluate diagnostic accuracy. A panel of serum miRNAs (miR-125b, miR-223, miR-27a, and miR-26a) used in conjunction with AFP helped differentiate HCC patients from those in the non-cancer group after adjusting for age and gender, with the area under the curve of 0.870. In addition, the use of miR-125b/miR-27a panel differentiated HBV-related early-stage HCC with a high sensitivity (80.0 %) and specificity (87.2 %) in AFP-negative (−) subjects. A combination of serum miR-125b, miR-223, miR-27a, and miR-26a as a second-line tests could help detect HCC in AFP (−) subjects. The panel of miR-125b/miR-27a/AFP had a higher sensitivity and specificity for diagnosis of early-stage HCC as compared to that of a single marker.
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影响因子:
--
作者:
Wang, Li;Yao, Min;Dong, Zhizhen;Zhang, Yun;Yao, Dengfu
通讯作者:
Yao, Dengfu
影响因子:
3.7
作者:
Tan Y;Ge G;Pan T;Wen D;Chen L;Yu X;Zhou X;Gan J
通讯作者:
Gan J
影响因子:
1.4
作者:
Mingchen Ba;H. Long;Yun-Qiang Tang;S. Cui
通讯作者:
Mingchen Ba;H. Long;Yun-Qiang Tang;S. Cui
影响因子:
3.1
作者:
A. Maringhini;M. Cottone;E. Sciarrino;M. P. MarcenÒ;F. Seta;G. Fusco;Fortunato Rinaldi;L. Pagliaro
通讯作者:
A. Maringhini;M. Cottone;E. Sciarrino;M. P. MarcenÒ;F. Seta;G. Fusco;Fortunato Rinaldi;L. Pagliaro
DOI:
10.1042/cs20100297
发表时间:
2011-03
期刊:
Clinical science (London, England : 1979)
影响因子:
--
作者:
Gui J;Tian Y;Wen X;Zhang W;Zhang P;Gao J;Run W;Tian L;Jia X;Gao Y
通讯作者:
Gao Y