Evidence map›Paper›PMID 33690683›Full record

ArticlePloS one2021

Cell-free microRNA-1246 in different body fluids as a diagnostic biomarker for esophageal squamous cell carcinoma.

Isamu Hoshino, Fumitaka Ishige, Yosuke Iwatate, Hisashi Gunji, Naoki Kuwayama, Yoshihiro Nabeya, Hajime Yokota, Nobuyoshi Takeshita, Keiko Iida, Hiroki Nagase and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Isamu HoshinoDivision of Gastroenterological Surgery, Chiba Cancer Center, Chiba, Japan.ORCID 0000-0002-8156-1752
Fumitaka IshigeDepartment of Hepatobiliary and Pancreatic Surgery, Chiba Cancer Center, Chiba, Japan.
Yosuke IwatateDepartment of Hepatobiliary and Pancreatic Surgery, Chiba Cancer Center, Chiba, Japan.
Hisashi GunjiDivision of Gastroenterological Surgery, Chiba Cancer Center, Chiba, Japan.
Naoki KuwayamaDivision of Gastroenterological Surgery, Chiba Cancer Center, Chiba, Japan.
Yoshihiro NabeyaDivision of Gastroenterological Surgery, Chiba Cancer Center, Chiba, Japan.
Hajime YokotaDepartment of Diagnostic Radiology and Radiation Oncology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Nobuyoshi TakeshitaDivision of Surgical Technology, National Cancer Center Hospital East, Chiba, Japan.
Keiko IidaDepartment of Frontier Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Hiroki NagaseLaboratory of Cancer Genetics, Chiba Cancer Center Research Institute, Chiba, Japan.
Hisahiro MatsubaraDepartment of Frontier Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Chiba Cancer Center · JPChiba University · JPNational Cancer Center Hospital East · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esophageal squamous cell carcinoma is a malignant tumor with unfavorable prognosis. In this study, we investigated the usefulness of microRNA (miR)-1246 detection in various body fluids as a biomarker for this disease. A total of 72 patients with esophageal squamous cell carcinoma were enrolled, and their blood, urine, and saliva samples were collected prior to treatment. Reverse transcription-polymerase chain reaction of miR-1246 was performed, and pre- and postoperative and intraday fluctuations in its expression were examined. The expression of miR-1246 in the blood and urine was significantly higher in the patients with esophageal squamous cell carcinoma than in 50 healthy control subjects. Receiver operating characteristic curves showed that the area under the curve values were 0.91 (sensitivity 91.7%, specificity 76.0%), 0.82 (sensitivity 90.3%, specificity 62.0%), and 0.80 (sensitivity 83.3%, specificity 66.0%) in the serum, urine, and saliva, respectively. A relatively high diagnostic performance of miR-1246 was observed in all samples, which was better than that of the existing biomarkers squamous cell carcinoma antigen, carcinoembryonic antigen, and cytokeratin 19 fragment. No clear correlation was observed in the levels of miR-1246 expression among the three body fluids. Postoperatively, serum samples displayed significantly decreased miR-1246 levels. Although not significant, changes in the miR-1246 levels were observed at all collection times, with large fluctuations in the saliva. Meanwhile, serum miR-1246 expression was found to be associated with the disease prognosis. The results indicate that the levels of miR-1246 in the urine, saliva, and serum are a useful biomarker for esophageal squamous cell carcinoma and support the use of urine samples instead of blood samples for noninvasive diagnosis.

Indexed as

AgedAged, 80 and overBiomarkers, TumorBody FluidsCarcinoma, Squamous CellCirculating MicroRNADisease-Free SurvivalEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleGene Expression ProfilingHumansJapanMaleMicroRNAsMiddle AgedBiomarkers, TumorCirculating MicroRNAMicroRNAsMIRN1246 microRNA, human

Identifiers

PMID33690683
PMCPMC7946279
OpenAlexW3134361921

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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.