Evidence map›Paper›PMID 41168129›Full record

ArticleRNA biology2025

Serum-MiR-CanPred: deep learning framework for pan-cancer classification and miRNA-targeted drug discovery.

Naisarg Patel, Ankita Lawarde, Suhas Manikant Surisetti, Premkumar Thiruselvam, Prakash Lingasamy, Vino Sundararajan, Sajitha Lulu S, Andres Salumets, Vijayachitra Modhukur

Abstract read
In one paragraph

Article in RNA biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Naisarg PatelIntegrative Multiomics Lab, School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, India.
Ankita LawardeDepartment of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
Suhas Manikant SurisettiIntegrative Multiomics Lab, School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, India.
Premkumar ThiruselvamIntegrative Multiomics Lab, School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, India.
Prakash LingasamyDepartment of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0002-8826-4531
Vino SundararajanIntegrative Multiomics Lab, School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, India.ORCID 0000-0002-0015-8460
Sajitha Lulu SIntegrative Multiomics Lab, School of Bio Sciences and Technology, Vellore Institute of Technology, Vellore, India.ORCID 0000-0002-3392-4168
Andres SalumetsDepartment of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0002-1251-8160
Vijayachitra ModhukurDepartment of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.ORCID 0000-0002-7123-9903

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer diagnosis at an early stage is crucial for improving overall health outcomes. However, existing cancer diagnostic techniques are mostly invasive and tend to identify the disease only in its advanced stages. MicroRNAs (miRNAs), which are small non-coding RNAs involved in gene expression regulation, are stable in serum as circulating miRNAs and have potential as non-invasive biomarkers. However, their application in pan-cancer diagnostics and therapeutics is still largely unexplored. We developed Serum-MiR-CanPred, a deep learning framework using a multi-layer perceptron (MLP) trained on serum miRNA expression data from 20,271 samples across 12 cancer types and healthy controls from GEO databases. The model achieves robust pan-cancer classification (AUC = 96.87%, accuracy = 96%) with a consensus set of 88 miRNAs. Validation using external datasets demonstrated its generalizability and clinical potential. SHapley Additive exPlanations (SHAP) identified hsa-miR-5100 as a key biomarker, dysregulated in cancers including lung, bladder, and gastric carcinomas. Pathway analysis linked these miRNAs to cancer-related processes like VEGFA-VEGFR2 signalling. Molecular docking of pre-mir-5100 with rDock, identified AC1MMYR2 as a potential high-affinity ligand, with binding stability confirmed by molecular dynamics simulations using GROMACS In conclusion, Serum-MiR-CanPred integrates explainable AI with molecular modelling, advancing miRNA-based diagnostics and drug discovery for precision oncology.

Indexed as

Biomarkers, TumorDeep LearningDrug DiscoveryMicroRNAsNeoplasmsGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMolecular Docking SimulationBiomarkers, TumorMicroRNAsartificial intelligencebiomarker discoveryCirculating miRNAdeep learningdrug repurposingmolecular dockingoncologypan-cancer predictionSHAP

Identifiers

PMID41168129
PMCPMC12578308

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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.