Evidence map›Paper›PMID 41080754›Full record

ArticleBiochemistry and biophysics reports2025

Machine learning and WGCNA reveal the PVT1/miR-143-3p/CDK1 ceRNA axis as a key regulator in NSCLC.

Arash Safarzadeh, Setareh Ataei, Arezou Sayad, Soudeh Ghafouri-Fard

Abstract read
In one paragraph

Article in Biochemistry and biophysics reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Arash SafarzadehDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Setareh AtaeiDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Arezou SayadDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Soudeh Ghafouri-FardDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Machine learning has provided novel tools for analysis of multi-omics data for subgroups recognition in cancer to reach a clinically meaningful classification of cancer and identification of potential biomarkers. In this work, we retrieved mRNA, lncRNA, miRNA and protein expression data of non-small cell lung cancer (NSCLC) samples and used different machine learning methods for biomarker selection, diagnostic validation, construction of competing endogenous RNA network, identification of the hub axes and drug prediction. Integration of multi-omics data and machine learning resulted in identification of CDK1, TOP2A, AURKA, TPX2, BUB1B, and CENPF as key biomarkers in NSCLC. We also identified the PVT1/miR-143-3p/CDK1 axis and its associated transcription factors (FOXC1, YY1, and GATA2) as a potential regulatory network for additional investigations. These findings increase the understanding of NSCLC molecular processes and provide a foundation for developing targeted therapies and diagnostic tools.

Indexed as

CDK1Machine learningmiR-143–3pNon-small cell lung cancerPVT1

Identifiers

PMID41080754
PMCPMC12514524

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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.