Evidence map›Paper›PMID 41044606›Full record

ReviewCancer cell international2025

Salivary genetic biomarkers of lung cancer: a systematic review and meta-analysis of the diagnostic accuracy.

Maryam Koopaie, Mahnaz Fatahzadeh, Sajad Kolahdooz

Abstract readReview
In one paragraph

Review in Cancer cell international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Maryam KoopaieDepartment of Oral Medicine, School of Dentistry, Tehran University of Medical Sciences, North Kargar, 14395 -433, Tehran, 14399-55991, Iran. mariakoopaie@gmail.com.
Mahnaz FatahzadehDivision of Oral Medicine, Department of Oral Medicine, Rutgers School of Dental Medicine, 110 Bergen Street, Newark, NJ, 07103, USA.
Sajad KolahdoozUniversal Scientific Education and Research Network (USERN), Tehran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConsidering the elevated mortality linked to lung cancer and the constraints of diagnostic and screening techniques, non-invasive biomarkers offer a promising alternative for early diagnosis. This systematic review and meta-analysis investigated the diagnostic accuracy of salivary genetic biomarkers for lung cancer.

methodsWe searched for pertinent keywords in the Cochrane Library, Embase, LIVIVO, MEDLINE, Web of Science, Scopus, and Google Scholar for relevant studies. A systematic review was performed, and data were extracted from the eligible studies. The methodological quality of the studies included in this review was assessed using the Quality Assessment tool for Diagnostic Accuracy Studies-2 (QUADAS-2). The split component synthesis method was used to determine sensitivity, specificity, likelihood ratios, and diagnostic odds ratios. Studies were classified into three categories based on the type of biomarkers used: the single salivary biomarker model, the multiple salivary biomarker model (using multiple salivary biomarkers), and the mixed biomarker model (combining salivary biomarkers with other data, such as blood biomarkers or demographic data). By synthesizing data from six studies, including single, multiple, and mixed biomarker models, the study aimed to evaluate the diagnostic accuracy of these models.

resultsThe findings indicate that single-salivary biomarker models exhibit moderate diagnostic performance, with sensitivity and specificity of 0.72 and 0.73, respectively. However, multiple salivary biomarker models demonstrate improved diagnostic accuracy (sensitivity: 0.88, specificity: 0.75), supporting the use of multiple salivary biomarkers to increase accuracy and reduce false-positive results. Mixed models using a combination of salivary and blood biomarkers outperformed other models, achieving a diagnostic odds ratio of 115.66, with sensitivity at 0.92 and specificity at 0.91.

conclusionsOur findings show that the mixed biomarker model (model using salivary and blood genetic biomarkers) yields the highest diagnostic odds ratio and area under the curve, making it the most efficacious diagnostic approach among the models analyzed.

Indexed as

BiomarkerDiagnosisGenetic markersLung cancerLung neoplasmsMeta-analysisMicroRNAsMouthMRNAsNon-small cell lung cancerSalivaSystematic review

Identifiers

PMID41044606
PMCPMC12495827

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.