Evidence map›Paper›PMID 41461789›Full record

ArticleScientific reports2025

Investigating the role of MYLK2 in breast cancer prognosis and assessing its clinical application value.

Zhitang Wang, Yazhen Cai, Debo Chen

Abstract readValidation Study
In one paragraph

Article in Scientific 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

The trial behind it

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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.

Zhitang WangDepartment of Breast, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, 362000, Fujian, China.
Yazhen CaiMedical Records Department of Quanzhou Maternal, Child Health Hospital (Quanzhou Children's Hospital), Quanzhou, 362000, Fujian, China.
Debo ChenDepartment of Breast, The First Hospital of Quanzhou Affiliated to Fujian Medical University, Quanzhou, 362000, Fujian, China. Chendb123@gmail.com.

Funding

Startup Fund for scientific research, Fujian Medical University 2022QH1259
6 · The paper itself

Abstract

objectiveThis study aims to investigate the mechanistic role of MYLK2 (myosin light chain kinase 2) in breast cancer and assess its potential as a prognostic biomarker for clinical applications.

methodsWe performed a comprehensive analysis using gene expression data from breast cancer patients in The Cancer Genome Atlas (TCGA) database. Kaplan-Meier survival analysis and multivariate Cox regression models were employed to evaluate the association between MYLK2 expression levels and patient survival outcomes.

resultsOur findings demonstrate that MYLK2 is significantly overexpressed in tumor tissues compared to normal adjacent tissues (P < 0.05). Kaplan-Meier survival analysis revealed that high MYLK2 expression correlates with poorer overall survival (OS), progression-free survival (PFS), and disease-specific survival (DSS) (P < 0.05). Furthermore, multivariate Cox regression analysis identified MYLK2 as an independent prognostic factor for adverse outcomes in breast cancer patients.

conclusionThis study elucidates the critical biological functions of MYLK2 in breast cancer, suggesting that it may serve as a promising prognostic biomarker. These findings provide new insights for early diagnosis and treatment strategies in breast cancer management.

Indexed as

Breast NeoplasmsMyosin-Light-Chain KinaseBiomarkers, TumorCalcium-Binding ProteinsComputational BiologyFemaleGene Expression Regulation, NeoplasticHumansMolecular Targeted TherapyPrognosisProtein Interaction MapsTumor MicroenvironmentBiomarkers, TumorCalcium-Binding ProteinsMYLK protein, humanMyosin-Light-Chain KinaseBreast cancerClinical application valueMYLK2Prognosis

Identifiers

PMID41461789
PMCPMC12749863

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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.