Oncotarget

Research Papers:

Examining plasma microRNA markers for colorectal cancer at different stages

Yan Sun, Yuexin Liu, David Cogdell, George A. Calin, Baocun Sun, Scott Kopetz, Stanley R. Hamilton and Wei Zhang _

PDF  |  HTML  |  Supplementary Files  |  How to cite

Oncotarget. 2016; 7:11434-11449. https://doi.org/10.18632/oncotarget.7196

Metrics: PDF 2160 views  |   HTML 4154 views  |   ?  


Abstract

Yan Sun1,5, Yuexin Liu1, David Cogdell1, George A. Calin2,4, Baocun Sun5, Scott Kopetz3, Stanley R. Hamilton1, Wei Zhang1,4

1Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

2Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

3Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

4The Center for RNA Interference and Non-Coding RNAs, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

5Department of Pathology, Tianjin Medical University Cancer Institute and Hospital, Tianjin 300060, China

Correspondence to:

Wei Zhang, e-mail: [email protected]

Yan Sun, e-mail: [email protected]

Keywords: microRNA, biomarker, plasma, colorectal cancer, stage

Received: September 23, 2015     Accepted: January 23, 2016     Published: February 04, 2016

ABSTRACT

Circulating microRNAs (miRNAs) have emerged as promising biomarkers; however, few miRNAs have been reproducible and can be used in clinical practice. In this study, we screened the levels of 754 miRNAs using TaqMan array in 50 individual plasma samples from 10 demographically matched healthy controls and 40 colorectal cancer (CRC) patients (10 each of stage I–IV) and identified 22 miRNAs associated with the presence of and stages of CRC. Then we performed the validation for 11 miRNAs in an independent cohort including 187 CRC cases and 47 healthy controls. Comprehensive analyses showed that plasma miR-96 distinguished stage I–IV CRC from healthy controls with an area under curve (AUC) of 0.740; miR-203 separated stage III–IV CRC patients from stage I–II with an AUC of 0.757; and miR-141 differentiated stage IV CRC from stage I–III patients with an AUC of 0.851. Survival analyses showed that plasma miR-96 and miR-200b were independent prognostic factors for overall survival. Thus, we propose four miRNAs (miR-96, miR-203, miR-141 and miR-200b) as clinically validated circulating biomarkers for CRC prognosis that warrant further evaluation for clinical utility.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 7196