Evidence map›Paper›PMID 28333958›Full record

ArticlePloS one2017

Targeted deep sequencing of plasma circulating cell-free DNA reveals Vimentin and Fibulin 1 as potential epigenetic biomarkers for hepatocellular carcinoma.

Reetta Holmila, Athena Sklias, David C Muller, Davide Degli Esposti, Paule Guilloreau, James Mckay, Suleeporn Sangrajrang, Petcharin Srivatanakul, Pierre Hainaut, Philippe Merle and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-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

32 citing papers in PubMed, 54 citations in OpenAlex.

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  12. Using cell-free DNA for HCC surveillance and prognosis.JHEP reports : innovation in hepatology · 2021
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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

12 authors at 4 institutions in 2 countries.

Reetta HolmilaEpigenetics group, International Agency for Research on Cancer (IARC), Lyon, France.
Athena SkliasEpigenetics group, International Agency for Research on Cancer (IARC), Lyon, France.
David C MullerGenetic Epidemiology group, International Agency for Research on Cancer (IARC), Lyon, France.
Davide Degli EspostiEpigenetics group, International Agency for Research on Cancer (IARC), Lyon, France.
Paule GuilloreauCroix-Rousse Hospital, Lyon, France.
James MckayGenetic Cancer Susceptibility group, International Agency for Research on Cancer (IARC), Lyon, France.
Suleeporn SangrajrangMolecular Epidemiology Section, National Cancer Institute, Bangkok, Thailand.
Petcharin SrivatanakulMolecular Epidemiology Section, National Cancer Institute, Bangkok, Thailand.
Pierre HainautInstitut Albert Bonniot, INSERM Unité 823, La Tronche, France.
Philippe MerleCroix-Rousse Hospital, Lyon, France.
Zdenko HercegEpigenetics group, International Agency for Research on Cancer (IARC), Lyon, France.
Andre Nogueira da CostaMolecular mechanisms and biomarkers group, International Agency for Research on Cancer (IARC), Lyon, France.
Centre International de Recherche sur le Cancer · FRHôpital de la Croix-Rousse · FRNational Cancer Institute of Thailand · THInstitut pour l'avancée des biosciences · FR

Funding

World Health Organization 001
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the second most common cause of cancer death worldwide, but is still lacking sensitive and specific biomarkers for early diagnosis and prognosis. In this study, we applied targeted massively parallel semiconductor sequencing to assess methylation on a panel of genes (FBLN1, HINT2, LAMC1, LTBP1, LTBP2, PSMA2, PSMA7, PXDN, TGFB1, UBE2L3, VIM and YWHAZ) in plasma circulating cell-free DNA (cfDNA) and to evaluate the potential of these genes as HCC biomarkers in two different series, one from France (42 HCC cases and 42 controls) and one from Thailand (42 HCC cases, 26 chronic liver disease cases and 42 controls). We also analyzed a set of HCC and adjacent tissues and liver cell lines to further compare with 'The Cancer Genome Atlas' (TCGA) data. The methylation in cfDNA was detected for FBLN1, PSMA7, PXDN and VIM, with differences in methylation patterns between cases and controls for FBLN1 and VIM. The average methylation level across analyzed CpG-sites was associated with higher odds of HCC for VIM (1.48 [1.02, 2.16] for French cases and 2.18 [1.28, 3.72] for Thai cases), and lower odds of HCC for FBLN1 (0.89 [0.76, 1.03] for French cases and 0.75 [0.63, 0.88] for Thai cases). In conclusion, our study provides evidence that changes in VIM and FBLN1 methylation levels in cfDNA are associated with HCC and could represent useful plasma-based biomarkers. Also, the potential to investigate methylation patterns in cfDNA could bring new strategies for HCC detection and monitoring high-risk groups and response to treatment.

Indexed as

BiomarkersCalcium-Binding ProteinsCarcinoma, HepatocellularDNADNA MethylationEpigenomicsGenetic MarkersHigh-Throughput Nucleotide SequencingHumansLiver NeoplasmsPrognosisVimentinBiomarkersCalcium-Binding ProteinsDNAfibulinGenetic MarkersVimentin

Identifiers

PMID28333958
PMCPMC5363871
OpenAlexW2598108680

What OpenQuestion holds

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LicenceCC BY
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.