Evidence map›Paper›PMID 24803312›Full record

ArticleInternational journal of cancer2015

Osteopontin and latent-TGF β binding-protein 2 as potential diagnostic markers for HBV-related hepatocellular carcinoma.

Andre Nogueira da Costa, Amelie Plymoth, Daniela Santos-Silva, Sandra Ortiz-Cuaran, Suzy Camey, Paule Guilloreau, Suleeporn Sangrajrang, Thiravud Khuhaprema, Maimuna Mendy, Olufunmilayo A Lesi and 8 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 7% of its field
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

44 citing papers in PubMed, 2 syntheses or guidelines pooled it, 60 citations in OpenAlex.

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  16. The Biomarkers for Predicting Viral HepatitisAssociated Hepatocellular Carcinoma.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2022
    Article
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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

18 authors at 12 institutions in 9 countries.

Andre Nogueira da CostaInternational Agency for Research on Cancer, Lyon, France.
Amelie Plymoth
Daniela Santos-Silva
Sandra Ortiz-Cuaran
Suzy Camey
Paule Guilloreau
Suleeporn Sangrajrang
Thiravud Khuhaprema
Maimuna Mendy
Olufunmilayo A Lesi
Hee-Kyung Chang
Jin-Kyoung Oh
Duk-Hee Lee
Hai-Rim Shin
Gregory D Kirk
Philippe Merle
Laura Beretta
Pierre Hainaut
Centre International de Recherche sur le Cancer · FRNational Cancer Institute of Thailand · THCentre de Recherche en Cancérologie de Lyon · FRHôpital de la Croix-Rousse · FRJohns Hopkins Medicine · USKarolinska Institutet · SEKosin University · KRKyungpook National University · KRLagos University Teaching Hospital · NGNational Cancer Center · USThe University of Texas MD Anderson Cancer Center · USWorld Health Organization Regional Office for the Western Pacific · PH

Funding

Novel markers for HCV-related HCCR01DK066840 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BERETTA, LAURA · 2004 to 2010
$2.0M
Markers for HCV-related HCC: plasma profiling, targeted strategies and validationR01CA120719 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BERETTA, LAURA · 2009 to 2013
$1.7M
NCI NIH HHS R01 CA120719NIDDK NIH HHS R01 DK066840World Health Organization 001
6 · The paper itself

Abstract

Chronic Hepatitis B (HB) is the main risk factor for chronic liver disease (CLD) and hepatocellular carcinoma (HCC) in many low-resource countries, where diagnosis is constrained by lack of clinical, histopathological and biomarker resources. We have used proteomics to detect plasma biomarkers that outperform α-Fetoprotein (AFP), the most widely used biomarker for HCC diagnosis in low-resource contexts. Deep-plasma proteome analysis was performed in HCC patients, patients with CLD and in HB-carrier controls from Thailand (South-East Asia) and The Gambia (West-Africa). Mass spectrometry profiling identified latent-transforming growth factor β binding-protein 2 (LTBP2) and Osteopontin (OPN) as being significantly elevated in HCC versus CLD and controls. These two proteins were further analyzed by ELISA in a total of 684 plasma samples, including 183 HCC, 274 CLD and 227 asymptomatic controls. When combined, LTBP2 and OPN showed an area under the receiver operating curve of 0.85 in distinguishing HCC from CLD in subjects with AFP <20 ng/mL. In a prospective cohort of 115 CLD patients from Korea, increased plasma levels of LTBP2 and/or OPN were detected in plasma collected over 2 years prior to diagnosis in 21 subjects who developed HCC. Thus, the combination of LTBP2 and OPN outperformed AFP for diagnosis and prediction of HCC and may therefore improve biomarker-based detection of HBV-related HCC.

Indexed as

Area Under CurveBiomarkers, TumorCarcinoma, HepatocellularCase-Control StudiesEarly Detection of CancerHepatitis B, ChronicHumansLatent TGF-beta Binding ProteinsLiver NeoplasmsOsteopontinPovertyROC CurveBiomarkers, TumorLatent TGF-beta Binding ProteinsLTBP2 protein, humanOsteopontinbiomarkerschronic liver diseasehepatocellular carcinomaLTBP2osteopontin

Identifiers

PMID24803312
PMCPMC4617682
OpenAlexW2119908372

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.