Evidence map›Paper›PMID 29632649›Full record

ArticleOncotarget2018

Circulating miR-106b-3p, miR-101-3p and miR-1246 as diagnostic biomarkers of hepatocellular carcinoma.

Farzaneh Moshiri, Alessandro Salvi, Laura Gramantieri, Angelo Sangiovanni, Paola Guerriero, Giuseppina De Petro, Cristian Bassi, Laura Lupini, Arash Sattari, Douglas Cheung and 12 more

Abstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 4 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  6. Experimental and therapeutic medicine · 2026
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3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Farzaneh MoshiriDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Alessandro SalviDepartment of Molecular and Translational Medicine, Division of Biology and Genetics, University of Brescia, Brescia, Italy.
Laura GramantieriCenter for Applied Biomedical Research, St. Orsola-Malpighi University Hospital, Bologna, Italy.
Angelo SangiovanniGastroenterology and Hepatology Division, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milano, Milan, Italy.
Paola GuerrieroDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Giuseppina De PetroDepartment of Molecular and Translational Medicine, Division of Biology and Genetics, University of Brescia, Brescia, Italy.
Cristian BassiDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Laura LupiniDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Arash SattariComprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.
Douglas CheungComprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.
Dario VenezianoComprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.
Giovanni NigitaComprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.
Ram C ShankaraiahDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Nazario PortolaniDepartment of Medical and Surgical Sciences, Surgical Clinic, University of Brescia, Brescia, Italy.
Paolo CarcoforoDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Francesca FornariCenter for Applied Biomedical Research, St. Orsola-Malpighi University Hospital, Bologna, Italy.
Luigi BolondiCenter for Applied Biomedical Research, St. Orsola-Malpighi University Hospital, Bologna, Italy.
Antonio FrassoldatiOncology Division, University Hospital of Ferrara, Cona (FE), Italy.
Silvia SabbioniDepartment of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
Massimo ColomboGastroenterology and Hepatology Division, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milano, Milan, Italy.
Carlo M CroceComprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.
Massimo NegriniDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Molecular Mechanisms of Cachexia in Lung CancerR01CA190740 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M, NANASINKAM, SERGE PATRICK · 2015 to 2019
$2.1M
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA190740
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most common liver cancer and second leading cause of cancer related death worldwide. Most HCCs occur in a damaged cirrhotic background and it may be difficult to discriminate between regenerative nodules and early HCCs. No dependable molecular biomarker exists for the early detection of HCC. MicroRNAs (miRNAs) have attracted attention as potential blood-based biomarkers. To identify circulating miRNAs with diagnostic potential in HCC, we performed preliminary RNAseq studies on plasma samples from a small set of HCC patients, cirrhotic patients and healthy controls. Then, out of the identified miRNAs, we investigated miR-101-3p, miR-106b-3p, miR-1246 and miR-411-5p in plasma of independent HCC patients' cohorts. The use of droplet digital PCR (ddPCR) confirmed the aberrant levels of these miRNAs. The diagnostic performances of each miRNA and their combinations were measured using Receiver Operating Characteristic (ROC) curve analyses: a classifier consisting of miR-101-3p, miR-1246 and miR-106b-3p produced the best diagnostic precision in plasma of HCC vs. cirrhotic patients (AUC = 0.99). A similar performance was found when the levels of miRNAs of HCC patients were compared to healthy controls (AUC = 1.00). We extended the analyses of the same miRNAs to serum samples. In serum of HCC vs. cirrhotic patients, the combination of miR-101-3p and miR-106b-3p exhibited the best diagnostic accuracy with an AUC = 0.96. Thus, circulating miR-101-3p, miR-106b-3p and miR-1246, either individually or in combination, exhibit a considerable potential value as diagnostic biomarkers of HCC.

Indexed as

circulating microRNAcirrhosisdiagnostic biomarkershepatocellular carcinoma

Identifiers

PMID29632649
PMCPMC5880609

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.