Evidence map›Paper›PMID 41070737›Full record

Observational studyFuture oncology (London, England)2025

hsa-miR-144-3p and hsa-miR-4262 are exosomal biomarkers and function as tumor suppressors in HCMV positive brain tumor.

Muhammad Shahbaz Haris, Muhammad Zahid Hussain, Azhar Mehmood, Mahmood Akhtar Kayani, Ishrat Mahjabeen

Abstract readObservational Study
In one paragraph

Observational study in Future oncology (London, England), 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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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Muhammad Shahbaz HarisCancer Genetics & Epigenetics Research Group, Department of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.
Muhammad Zahid HussainDepartment of Rheumatology, CMH Multan Institute of Medical Sciences, Multan, Pakistan.
Azhar MehmoodCancer Genetics & Epigenetics Research Group, Department of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.ORCID 0000-0002-8094-7557
Mahmood Akhtar KayaniCancer Genetics & Epigenetics Research Group, Department of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.ORCID 0000-0001-9886-180X
Ishrat MahjabeenCancer Genetics & Epigenetics Research Group, Department of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.ORCID 0000-0002-6392-672X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe present retrospective observational study was designed to explore the expression deregulation of exosomal microRNAs, hsa-miR-144-3p, hsa-miR-4262, and related genes in brain tumor patients.

methodsExosomes were extracted from 400 brain tumor patients and 400 controls and characterized using DLS, TEM, and ELISA. Quantitative PCR was used to check the expression level of hsa-miR-144-3p, hsa-miR-4262, phosphatidylinositol-3-kinase (PI3K) and AKT kinase (AKT) in study cohort. CMV level in brain tumor patients was checked by quantifying UL83.

resultsData analysis showed significant deregulation of hsa-miR-144-3p (p < 0.0001), hsa-miR-4262 (p < 0.0001), PI3K (p < 0.0001), and AKT (p < 0.0001) in brain tumor patients. Conclusions: ROC curve analysis showed that deregulation of hsa-miR-144-3p, hsa-miR-4262, PI3K, and AKT may act as good diagnostic markers for brain tumor patients.

Indexed as

Biomarkers, TumorBrain NeoplasmsCytomegalovirus InfectionsExosomesMicroRNAsAdultAgedCytomegalovirusFemaleGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansMaleMiddle AgedPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktBiomarkers, TumorMicroRNAsMIRN144 microRNA, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktbrain tumorexosomal microRNAExtracellular vesiclesHCMVquantitative PCR

Identifiers

PMID41070737
PMCPMC12582130

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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.