Evidence map›Paper›PMID 36737651›Full record

ArticleScientific reports2023

A circulating microRNA panel as a novel dynamic monitor for oral squamous cell carcinoma.

Yudan Piao, Seung-Nam Jung, Mi Ae Lim, Chan Oh, Yan Li Jin, Hae Jong Kim, Quoc Khanh Nguyen, Jae Won Chang, Ho-Ryun Won, Bon Seok Koo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

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  17. Oral Squamous Cell Carcinoma: Focus on Biomarkers for Screening.Journal of dentistry (Shiraz, Iran) · 2024
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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

10 authors at 1 institution in 1 country.

Yudan PiaoDepartment of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
Seung-Nam JungDepartment of Otolaryngology-Head and Neck Surgery, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea.
Mi Ae LimDepartment of Otolaryngology-Head and Neck Surgery, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea.
Chan OhDepartment of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
Yan Li JinDepartment of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
Hae Jong KimDepartment of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
Quoc Khanh NguyenDepartment of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
Jae Won ChangDepartment of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.
Ho-Ryun Won *Department of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea. hryun83@cnuh.co.kr.
Bon Seok Koo *Department of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea. bskoo515@cnuh.co.kr.
Chungnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral squamous cell carcinoma (OSCC) has high recurrence and mortality rates despite advances in diagnosis and treatment. Therefore, it is necessary to identify new biomarkers for early detection, efficient monitoring, and prognosis prediction. Since microRNA (miRNA) is stable and detectable in serum, it has been reported to inform the diagnosis and monitor disease progression through liquid biopsy. In this study, a circulating specific miRNA panel in OSCC patients was developed, and its usefulness as a dynamic monitor was validated. Small RNAs were extracted from the serum of OSCC patients (n = 4) and normal controls (n = 6) and profiled using next-generation sequencing. NGS identified 42 differentially expressed miRNAs (DEmiRNAs) in serum between patients with OSCC and healthy controls, with threefold differences (p < 0.05). Combining the 42 DEmiRNAs and The Cancer Genome Atlas (TCGA) databases OSCC cohort, 9 overlapping DEmiRNAs were screened out. Finally, 4 significantly up-regulated miRNAs (miR-92a-3p, miR-92b-3p, miR-320c and miR-629-5p) were identified from OSCC patients via validation in the Chungnam National University Hospital cohort. Application of the specific miRNA panel for distinguishing OSCC patients from healthy controls produced specificity and sensitivity of 97.8 and 74%, respectively. In addition, the serum levels of these 4 miRNAs significantly decreased after complete surgical resection and increased after recurrence. We suggest that circulating 4-miRNA panel might be promising non-invasive predictors for diagnosing and monitoring the progression of patients with OSCC.

Indexed as

Circulating MicroRNAMicroRNAsMouth NeoplasmsSquamous Cell Carcinoma of Head and NeckBiomarkers, TumorGene Expression ProfilingHumansBiomarkers, TumorCirculating MicroRNAMicroRNAsMIRN629 microRNA, human

Identifiers

PMID36737651
PMCPMC9898506
OpenAlexW4319080474

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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.