Evidence map›Paper›PMID 31658043›Full record

ArticleCancer biomarkers : section A of Disease markers2019

Circulating plasma microRNA signature for the diagnosis of cervical cancer.

Ge Ma, Guoxin Song, Xuan Zou, Xia Shan, Qingxie Liu, Tiansong Xia, Xin Zhou, Wei Zhu

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 3 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

37 citing papers in PubMed, 3 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Liquid Biopsy Biomarkers for Cervical Cancer: A Systematic Review.International journal of molecular sciences · 2025
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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

8 authors at 2 institutions in 1 country.

Ge MaBreast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China.
Guoxin SongDepartment of Pathology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Xuan ZouFirst Clinical College of Nanjing Medical University, Nanjing, Jiangsu, China.
Xia ShanDepartment of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Qingxie LiuDepartment of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Tiansong XiaBreast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China.
Xin ZhouDepartment of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Wei ZhuDepartment of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Nanjing Medical University · CNJiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine the utility of plasma microRNAs (miRNAs) as biomarkers in cervical cancer (CC).

methodsSome studies were conducted about the specific expression of plasma miRNAs in the diagnosis of CC. Plasma samples of 97 CC patients and 87 normal controls (NCs) were used to identify dysregulation of miRNAs in the training, testing, and external validation phases. Receiver operating characteristic (ROC) curves and area under the ROC curve (AUC) were used to evaluate the sensitivity and specificity of identified individual miRNAs and miRNA panels for the diagnosis of CC. Expression levels of specific miRNAs were also examined in plasma exosomes and tissue samples of CC patients.

resultsFour plasma miRNAs (miR-146a-5p, miR-151a-3p, miR-2110 and miR-21-5p) which showed up-regulation were identified and validated in CC patients. A panel of the four miRNAs were constructed as potential diagnostic markers for CC. The AUCs of the panel of these four-miRNAs for the training, testing, and external validation phases were 0.911, 0.774, and 0.786, respectively. miR-146a-5p and miR-21-5p levels were all up-regulated in CC tissue specimens, whereas miR-146a-5p, miR-151a-3p, and miR-2110 levels were up-regulated in plasma exosomes.

conclusionThe signature of the four-miRNAs identified in peripheral plasma is a promising novel biomarker for the diagnosis of CC.

Indexed as

Biomarkers, TumorCase-Control StudiesCirculating MicroRNAFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedUterine Cervical NeoplasmsBiomarkers, TumorCirculating MicroRNAcervical cancerdiagnosisexosomePlasma microRNAqRT-PCR

Identifiers

PMID31658043
PMCPMC12826395
OpenAlexW2981442203

What OpenQuestion holds

Textmetadata
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.