| Literature DB >> 26850373 |
Liang Li1, Jianguo Chen2, Xin Chen1, Jing Tang1, Huan Guo3, Xiaofeng Wang4, Ji Qian4, Guijuan Luo1, Fangping He5, Xiaomei Lu5, Yibo Ding6, Yingchen Yang7, Wentao Huang7, Guojun Hou7, Ximeng Lin7, Qin Ouyang7, Hengyu Li7, Ruoyu Wang8, Feng Jiang9, Rui Pu6, Jianhua Lu2, Mudan Jin7, Yexiong Tan1, Frank J Gonzalez10, Guangwen Cao6, Mengchao Wu8, Hao Wen5, Tangchun Wu3, Li Jin4, Lei Chen11, Hongyang Wang12.
Abstract
The extremely poor prognosis of patients with symptomatic hepatocellular carcinoma (HCC) diagnosed clinically at advanced stages suggests an urgent need for biomarkers that can be used for prospective surveillance and pre-clinical screening for early presence of pre-malignant lesions and tumors. In a retrospective longitudinal phase 3 biomarker study in seven medical centers of China, time-series and 6 months interval-serum samples were collected from chronic hepatitis B virus infected (CHB) patient cohorts at the pre-malignant or pre-clinical stages (average 6 months prior to clinical diagnosis) and CHB patients that did not develop cancer, and circulating miRNAs measured. A set of serum miRNAs including miR-193a-3p, miR-369-5p, miR-672, miR-429 and let-7i* were identified in pre-clinical HCC patients and have the potential to screen for CHB patients at high risk to develop HCC 6-12 months after miRNAs measurement. These circulating miRNAs combined with the conventional screening tools using α-fetoprotein and ultrasound, may have great promise for the prediction and prevention of HCC in high-risk populations.Entities:
Keywords: Biomarker; Circulating miRNAs; Hepatocellular carcinoma; Prediction; Prevention
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Year: 2016 PMID: 26850373 PMCID: PMC6594104 DOI: 10.1016/j.canlet.2016.01.028
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679