Evidence map›Paper›PMID 26779490›Full record

ArticleFrontiers in molecular biosciences2015

Tumor-Related Methylated Cell-Free DNA and Circulating Tumor Cells in Melanoma.

Francesca Salvianti, Claudio Orlando, Daniela Massi, Vincenzo De Giorgi, Marta Grazzini, Mario Pazzagli, Pamela Pinzani

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  15. PD-L1 Detection on Circulating Melanoma Cells.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Emerging Biomarkers in Cutaneous Melanoma.Molecular diagnosis & therapy · 2018
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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

7 authors at 1 institution in 1 country.

Francesca SalviantiDepartment of Clinical, Experimental and Biomedical Sciences, University of Florence Florence, Italy.
Claudio OrlandoDepartment of Clinical, Experimental and Biomedical Sciences, University of Florence Florence, Italy.
Daniela MassiDivision of Pathology, Department of Surgery and Translational Medicine, University of Florence Florence, Italy.
Vincenzo De GiorgiDivision of Dermatology, Department of Surgery and Traslational Medicine, University of Florence Florence, Italy.
Marta GrazziniDivision of Dermatology, Department of Surgery and Traslational Medicine, University of Florence Florence, Italy.
Mario PazzagliDepartment of Clinical, Experimental and Biomedical Sciences, University of Florence Florence, Italy.
Pamela PinzaniDepartment of Clinical, Experimental and Biomedical Sciences, University of Florence Florence, Italy.
University of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solid tumor release into the circulation cell-free DNA (cfDNA) and circulating tumor cells (CTCs) which represent promising biomarkers for cancer diagnosis. Circulating tumor DNA may be studied in plasma from cancer patients by detecting tumor specific alterations, such as genetic or epigenetic modifications. Ras association domain family 1 isoform A (RASSF1A) is a tumor suppressor gene silenced by promoter hypermethylation in a variety of human cancers including melanoma. The aim of the present study was to assess the diagnostic performance of a tumor-related methylated cfDNA marker in melanoma patients and to compare this parameter with the presence of CTCs. RASSF1A promoter methylation was quantified in cfDNA by qPCR in a consecutive series of 84 melanoma patients and 68 healthy controls. In a subset of 68 cases, the presence of CTCs was assessed by a filtration method (Isolation by Size of Epithelial Tumor Cells, ISET) as well as by an indirect method based on the detection of tyrosinase mRNA by RT-qPCR. The distribution of RASSF1A methylated cfDNA was investigated in cases and controls and the predictive capability of this parameter was assessed by means of the area under the ROC curve (AUC). The percentage of cases with methylated RASSF1A promoter in cfDNA was significantly higher in each class of melanoma patients (in situ, invasive and metastatic) than in healthy subjects (Pearson chi-squared test, p < 0.001). The concentration of RASSF1A methylated cfDNA in the subjects with a detectable quantity of methylated alleles was significantly higher in melanoma patients than in controls. The biomarker showed a good predictive capability (in terms of AUC) in discriminating between melanoma patients and healthy controls. This epigenetic marker associated to cfDNA did not show a significant correlation with the presence of CTCs, but, when the two parameters are jointly considered, we obtain a higher sensitivity of the detection of positive cases in invasive and metastatic melanomas. Our data suggest that cell-free tumor DNA and CTCs represent two complementary aspects of the liquid biopsy which may improve the diagnosis and the clinical management of melanoma patients.

Indexed as

cell-free DNAcirculating tumor cellsepigenetic markermelanomatumor marker

Identifiers

PMID26779490
PMCPMC4705904
OpenAlexW2222487251

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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.