Evidence map›Paper›PMID 31877923›Full record

ReviewGenes2019

Cell-Free DNA Methylation: The New Frontiers of Pancreatic Cancer Biomarkers' Discovery.

Mariarita Brancaccio, Francesco Natale, Geppino Falco, Tiziana Angrisano

Abstract readReview
In one paragraph

Review in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
–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

36 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Cell-Free DNA Hypermethylation in Patients with Acute Pancreatitis.International journal of molecular sciences · 2025
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  5. Article
  6. Review
  7. Article
  8. Article
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  11. HighZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Article
  12. Review
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  15. 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

4 authors.

Mariarita BrancaccioDepartment of Biology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Naples, Italy.ORCID 0000-0002-4161-512X
Francesco NataleDepartment of Biology, University of Naples Federico II, 80126 Naples, Italy.ORCID 0000-0001-5366-9005
Geppino FalcoDepartment of Biology, University of Naples Federico II, 80126 Naples, Italy.
Tiziana AngrisanoDepartment of Biology, University of Naples Federico II, 80126 Naples, Italy.ORCID 0000-0002-5940-5278

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is among the most lethal cancer types world-wide. Its high mortality is related to the difficulty in the diagnosis, which often occurs when the disease is already advanced. As of today, no early diagnostic tests are available, while only a limited number of prognostic tests have reached clinical practice. The main reason is the lack of reliable biomarkers that are able to capture the early development or the progression of the disease. Hence, the discovery of biomarkers for early diagnosis or prognosis of PDAC remains, de facto, an unmet need. An increasing number of studies has shown that cell-free DNA (cfDNA) methylation analysis represents a promising non-invasive approach for the discovery of biomarkers with diagnostic or prognostic potential. In particular, cfDNA methylation could be utilized for the identification of disease-specific signatures in pre-neoplastic lesions or chronic pancreatitis (CP), representing a sensitive and non-invasive method of early diagnosis of PDAC. In this review, we will discuss the advantages and pitfalls of cfDNA methylation studies. Further, we will present the current advances in the discovery of pancreatic cancer biomarkers with early diagnostic or prognostic potential, focusing on pancreas-specific (e.g.,

Indexed as

ADAMTS1 ProteinBiomarkers, TumorCarcinoma, Pancreatic DuctalCell-Free Nucleic AcidsDNA-Binding ProteinsDNA MethylationEpigenesis, GeneticHomeodomain ProteinsHumansLithostathineNeoplasm StagingPancreatic NeoplasmsPancreatitisPrognosisPromoter Regions, GeneticTranscription FactorsADAMTS1 ProteinBiomarkers, TumorBNC1 protein, humanCell-Free Nucleic AcidsCUX2 protein, humanDNA-Binding ProteinsHomeodomain ProteinsLithostathineREG1A protein, humanTranscription Factorsbiomarkercell-free DNAchronic pancreatitisDNA methylationearly diagnosisepigenetic signaturepancreatic cancerpre-neoplasticprognosis

Identifiers

PMID31877923
PMCPMC7017422

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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.