Evidence mapPaperPMID 41868101Full record

ReviewFrontiers in molecular biosciences2026

Artificial intelligence-based miRNA analysis for precision oncology: diagnostic and prognostic insights.

Tauqeer Zehra, Maryam Koopaie, Nishat Fatima, Gowhar Rashid, Iquebal Hasan, Zainab Siddiqui

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Tauqeer ZehraDepartment of Biotechnology, Era University, Lucknow, India.
Maryam KoopaieDepartment of Oral Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Nishat FatimaDepartment of Biotechnology, Era University, Lucknow, India.
Gowhar RashidDepartment of Clinical Biochemistry, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, India.
Iquebal HasanTanner College of Dental Medicine, University of Pikeville, Pikeville, KY, United States.
Zainab SiddiquiCenter for Disease Mapping and Therapeutic Research, Era University, Lucknow, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: MicroRNAs (miRNAs), small molecules that fine-tune gene activity, are consistently disrupted in cancer. Found stably in blood and other fluids, their unique cancer-associated patterns offer a promising route for non-invasive detection and monitoring. Merging artificial intelligence (AI) with miRNA analysis could revolutionize our understanding and treatment of cancer; however, reliably integrating these tools into clinics remains challenging. Methods: A multi-database search was executed until July 2025 using integrated miRNA-related descriptors and AI/ML ontologies such as support vector machine (SVM), random forest (RF), artificial neural network (ANN), logistic regression (LR), principal component analysis (PCA), and hierarchical clustering (HC), to interpret complex miRNA data in cancer. Our focus was on considering research article related to early cancer detection, prediction of patient outcomes, and guiding personalized treatments Findings: AI models analysing miRNA signatures demonstrate remarkable accuracy [area under the curve (AUC) often exceeding 0.90] in diagnosing various cancers, such as gastric, breast, and lung cancer (LC). For example, SVM proved highly effective for breast cancer (BC) detection. Crucially, AI helps identify small miRNA sets linked to cancer progression, such as a 3-miRNA combination (hsa-let-7i-3p, miR-362-3p, and miR-3651) that predicts disease stage across eight cancers. RF models achieved near-perfect AUCs (1.00) in some validation studies. AI also identifies miRNAs, such as a specific 5-miRNA group in BC, that signal resistance to chemotherapy. However, significant roadblocks persist: fragmented and non-standardized data, AI tools that exhibit disparate performance across demographic groups (evidenced by racial bias in mammography algorithms), and unaddressed validation gaps. Interpretation: The powerful combination of AI and miRNA biology is reshaping oncology. It enables earlier cancer detection, more accurate forecasts of disease course, and therapies tailored to the individual. Realizing this potential demands AI models that clinicians can understand and trust, diverse datasets to ensure tools work fairly for all patients, and close teamwork across disciplines to integrate these advances into real-world care. This convergence marks a pivotal shift towards proactive, precise, and accessible cancer management globally.

Indexed as

artificial intelligence (AI)biomarkerscancer diagnosisdeep learning (DL)machine learning (ML)miRNAprecision oncologyrandom forest (RF)

Identifiers

PMID41868101
PMCPMC13001116

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.