Evidence map›Paper›PMID 35557032›Full record

ArticleJournal of gynecologic oncology2022

Diagnostic performance of microRNA-34a, let-7f and microRNA-31 in epithelial ovarian cancer prediction.

Vivek Kumar, Sameer Gupta, Kachnar Varma, Amrita Chaurasia, Manisha Sachan

Open access · diamondAbstract read
In one paragraph

Article in Journal of gynecologic oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. The Role of microRNA in the Prognosis and Diagnosis of Ovarian Cancer.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

5 authors at 3 institutions in 1 country.

Vivek KumarDepartment of Biotechnology, Motilal Nehru National Institute of Technology Allahabad, Prayagraj, India.ORCID 0000-0002-2406-1954
Sameer GuptaDepartment of Surgical Oncology, King George Medical University, Lucknow, India.ORCID 0000-0002-1865-1640
Kachnar VarmaDepartment of Pathology, Motilal Nehru Medical College Allahabad, Prayagraj, India.ORCID 0000-0003-0072-7368
Amrita ChaurasiaDepartment of Gynaecology and Obstetrics, Motilal Nehru Medical College Allahabad, Prayagraj, India.ORCID 0000-0003-3123-5980
Manisha SachanDepartment of Biotechnology, Motilal Nehru National Institute of Technology Allahabad, Prayagraj, India. manishas@mnnit.ac.in.ORCID 0000-0001-9710-8808
Motilal Nehru Medical College · INMotilal Nehru National Institute of Technology · INKing George's Medical University · IN

Funding

Indian Council of Medical Research 5/13/58/2015/NCD-III
6 · The paper itself

Abstract

objectiveTo correlate the genome-wide methylation signature of microRNA genes with dysregulated expression of selected candidate microRNA in tissue and serum samples of epithelial ovarian cancer (EOC) and control using quantitative reverse transcription polymerase chain reaction (qRT-PCR), and evaluation of EOC predictive value of candidate microRNA at an early stage.

methodsWe performed Methylated DNA Immunoprecipitation coupled with NGS (MeDIP-NGS) sequencing of 6 EOC and 2 normal tissue samples of the ovary. Expression of selected microRNA from tissue (EOC=85, normal=30) and serum (EOC=50, normal=15) samples was evaluated using qRT-PCR. We conducted bioinformatics analysis to identify the candidate miRNA's potential target and functional role.

resultsMeDIP-NGS sequencing revealed hypermethylation of several microRNAs gene promoters. Three candidate microRNAs were selected (microRNA-34a, let-7f, and microRNA-31) from MeDIP-NGS data analysis based on log2FC and P-value. The relative expression level of microRNA-34a, let-7f, and microRNA-31 was found to be significantly reduced in early-stage EOC tissues and serum samples (p<0.0001). The receiver operating characteristic analysis of microRNA-34a, let-7f and miR-31 showed improved diagnostic value with area under curve(AUC) of 92.0 (p<0.0001), 87.9 (p<0.0001), and 85.6 (p<0.0001) and AUC of 82.7 (p<0.0001), 82.0 (p<0.0001), and 81.0 (p<0.0001) in stage III-IV and stage I-II EOC serum samples respectively. The integrated diagnostic performance of microRNA panel (microRNA-34a+let-7f+microRNA-31) in late-stage and early-stage serum samples was 95.5 and 96.9 respectively.

conclusionOur data correlated hypermethylation-associated downregulation of microRNA in EOC. In addition, a combined microRNA panel from serum could predict the risk of EOC with greater AUC, sensitivity, and specificity.

Indexed as

MicroRNAsNeoplasms, Glandular and EpithelialOvarian NeoplasmsBiomarkers, TumorCarcinoma, Ovarian EpithelialDown-RegulationFemaleGene Expression Regulation, NeoplasticHumansBiomarkers, TumorMicroRNAsMIRN31 microRNA, humanBiomarkerDiagnosisEpigeneticsmicroRNAOvarian Cancer

Identifiers

PMID35557032
PMCPMC9250857
OpenAlexW4225366167

What OpenQuestion holds

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LicenceCC BY-NC
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.