Evidence map›Paper›PMID 27716620›Full record

ArticleOncotarget2016

Circulating microRNAs found dysregulated in ex-exposed asbestos workers and pleural mesothelioma patients as potential new biomarkers.

Ilaria Bononi, Manola Comar, Andrea Puozzo, Mariarita Stendardo, Piera Boschetto, Sara Orecchia, Roberta Libener, Roberto Guaschino, Silvia Pietrobon, Manuela Ferracin and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. 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
5.4field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 67 citations in OpenAlex.

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  15. Asbestos induces mesothelial cell transformation via HMGB1-driven autophagy.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

14 authors at 4 institutions in 1 country.

Ilaria BononiDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, School of Medicine, University of Ferrara, Ferrara, Italy.
Manola ComarInstitute for Maternal and Child Health - IRCCS "Burlo-Garofolo"- Trieste, University of Trieste, Trieste, Italy.
Andrea PuozzoDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, School of Medicine, University of Ferrara, Ferrara, Italy.
Mariarita StendardoDepartment of Medical Sciences, School of Medicine, University of Ferrara, Ferrara, Italy.
Piera BoschettoDepartment of Medical Sciences, School of Medicine, University of Ferrara, Ferrara, Italy.
Sara OrecchiaMesothelioma BioBank, Pathology Unit and City Hospital, Alessandria, Italy.
Roberta LibenerMesothelioma BioBank, Pathology Unit and City Hospital, Alessandria, Italy.
Roberto GuaschinoTransfusion Medicine, City Hospital, Alessandria, Italy.
Silvia PietrobonDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, School of Medicine, University of Ferrara, Ferrara, Italy.
Manuela FerracinDepartment of Experimental, Diagnostic and Specialty Medicine - DIMES, University of Bologna, Bologna, Italy.
Massimo NegriniDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, School of Medicine, University of Ferrara, Ferrara, Italy.
Fernanda MartiniDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, School of Medicine, University of Ferrara, Ferrara, Italy.
Massimo BovenziClinical Unit of Occupational Medicine, Department of Medical Sciences, School of Medicine, University of Trieste, Trieste, Italy.
Mauro TognonDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, School of Medicine, University of Ferrara, Ferrara, Italy.
University of Ferrara · ITAzienda Sanitaria Locale Alessandria · ITUniversity of Trieste · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant pleural mesothelioma (MPM), a fatal cancer, is an occupational disease mostly affecting workers ex-exposed to asbestos fibers. The asbestos, a cancerogenic mineral of different chemical composition, was widely employed in western Countries in industrial manufactures of different types. MPM may arise after a long latency period, up to five decades. MPM is resistant to conventional chemo- and radio-therapies. Altogether, these data indicate that the identification of new and specific markers are of a paramount importance for an early diagnosis and treatment of MPM. In recent years, microRNAs expression was found dysregulated in patients, both in cancer cells and sera, affected by tumors of different histotypes, including MPM. Cell and circulanting microRNAs, found to be dysregulated in this neoplasia, were proposed as new biomarkers. It has been reported that circulating microRNAs are stable in biological fluids and could be employed as potential MPM biomarkers. In this investigation, circulating microRNAs (miR) from serum samples of MPM patients and workers ex-exposed to asbestos fibers (WEA) and healthy subjects (HS) were comparatively analyzed by microarray and RT-qPCR technologies. Our results allowed (i) to select MiR-3665, an endogenous stable microRNA, as the internal control to quantify in our analyses circulating miRNAs; to detect (ii) miR-197-3p, miR-1281 and miR 32-3p up-regulated in MPM compared to HS; (iii) miR-197-3p and miR-32-3p up-regulated in MPM compared to WEA; (iv) miR-1281 up-regulated in both MPM and WEA compared to HS. In conclusion, three circulating up-regulated microRNAs, i.e. miR-197-3p, miR-1281 and miR-32-3p are proposed as potential new MPM biomarkers.

Indexed as

Occupational HealthArea Under CurveAsbestosBiomarkers, TumorCase-Control StudiesCirculating MicroRNAGene Expression ProfilingHumansLung NeoplasmsMesotheliomaMesothelioma, MalignantMicroRNAsOccupational ExposureOligonucleotide Array Sequence AnalysisPleural NeoplasmsPredictive Value of TestsAsbestosBiomarkers, TumorCirculating MicroRNAMicroRNAsMIRN1281 microRNA, humanMIRN197 microRNA, humanMIRN32 microRNA, humanasbestosbiomarkermesotheliomamicroRNAworker

Identifiers

PMID27716620
PMCPMC5347725
OpenAlexW2528598919

What OpenQuestion holds

Textmetadata
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.