Circulating Plasma MiR-141 Is a Novel Biomarker for Metastatic Colon Cancer and Predicts Poor Prognosis

被引:346
作者
Cheng, Hanyin [1 ]
Zhang, Lina [2 ]
Cogdell, David E. [1 ]
Zheng, Hong [2 ]
Schetter, Aaron J. [3 ]
Nykter, Matti [4 ]
Harris, Curtis C. [3 ]
Chen, Kexin [2 ]
Hamilton, Stanley R. [1 ]
Zhang, Wei [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[2] Tianjin Med Univ Canc Inst & Hosp, Dept Epidemiol & Biostat, Tianjin, Peoples R China
[3] NCI, Human Carcinogenesis Lab, Ctr Canc Res, Bethesda, MD 20892 USA
[4] Tampere Univ Technol, Dept Signal Proc, FIN-33101 Tampere, Finland
来源
PLOS ONE | 2011年 / 6卷 / 03期
关键词
TUMOR-SUPPRESSOR GENE; COLORECTAL-CANCER; EXPRESSION; MICRORNAS; TARGETS; CELLS; ZEB1;
D O I
10.1371/journal.pone.0017745
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Colorectal cancer (CRC) remains one of the major cancer types and cancer related death worldwide. Sensitive, non-invasive biomarkers that can facilitate disease detection, staging and prediction of therapeutic outcome are highly desirable to improve survival rate and help to determine optimized treatment for CRC. The small non-coding RNAs, microRNAs (miRNAs), have recently been identified as critical regulators for various diseases including cancer and may represent a novel class of cancer biomarkers. The purpose of this study was to identify and validate circulating microRNAs in human plasma for use as such biomarkers in colon cancer. Methodology/Principal Findings: By using quantitative reverse transcription-polymerase chain reaction, we found that circulating miR-141 was significantly associated with stage IV colon cancer in a cohort of 102 plasma samples. Receiver operating characteristic (ROC) analysis was used to evaluate the sensitivity and specificity of candidate plasma microRNA markers. We observed that combination of miR-141 and carcinoembryonic antigen (CEA), a widely used marker for CRC, further improved the accuracy of detection. These findings were validated in an independent cohort of 156 plasma samples collected at Tianjin, China. Furthermore, our analysis showed that high levels of plasma miR-141 predicted poor survival in both cohorts and that miR-141 was an independent prognostic factor for advanced colon cancer. Conclusions/Significance: We propose that plasma miR-141 may represent a novel biomarker that complements CEA in detecting colon cancer with distant metastasis and that high levels of miR-141 in plasma were associated with poor prognosis.
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页数:8
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