Evidence map›Paper›PMID 42169120›Full record

ArticleWorld journal of surgical oncology2026

MicroRNA-563 as a potential biomarker in triple-negative breast cancer: impeding tumor progression by targeting ITGAV and epithelial-mesenchymal transition.

Xiaobo Li, Huiling Qin, Jing Zhai, Xingzhen Hu, Lan Liu

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Article in World journal of surgical oncology, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiaobo Li *Department of Pathology, The Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, Jilin, 133000, China.
Huiling Qin *Department of Rehabilitation Medicine, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, 533000, China.
Jing ZhaiRadiation Oncology Department, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Xingzhen HuDepartment of Radiology, Ningbo Yinzhou No.2 Hospital, No. 998 Qianhe North Road, Yinzhou District, Ningbo, 315192, China. Huxingzhenhxz@163.com.
Lan LiuDepartment of Pathology, The Affiliated Hospital of Yanbian University (Yanbian Hospital), Yanji, Jilin, 133000, China. Liulianll2026@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is characterized by its aggressive nature and limited treatment options, which contribute to a poor prognosis. However, the potential role of microRNA-563 (miR-563) in this malignancy remains unclear. This study investigates the tumor-suppressive role of miR-563 and its underlying mechanisms, proposing its potential as a novel biomarker in TNBC.

methodsThe expression of miR-563 was analyzed in clinical samples of TNBC in comparison to healthy controls and non-TNBC cases. Functional assays were conducted using TNBC cell lines. Bioinformatics prediction and luciferase reporter assays identified integrin subunit alpha-V (ITGAV) as a direct target, which was further validated through rescue experiments. Additionally, epithelial-mesenchymal transition (EMT) markers were assessed to elucidate the mechanistic pathway.

resultsMiR-563 was significantly downregulated in TNBC patients, demonstrating an area under the curve (AUC) of 0.895 for diagnosis. This downregulation correlated with advanced disease stage, lymph node metastasis, and poorer progression-free survival. Overexpression of miR-563 resulted in the suppression of TNBC cell proliferation, migration, and invasion. ITGAV was identified as a direct target of miR-563, and rescue experiments indicated a partial reversal of the tumor-suppressive effects of miR-563. Furthermore, miR-563 inhibited EMT, as evidenced by the upregulation of E-cadherin and downregulation of Vimentin.

conclusionsThese findings identify miR-563 as a crucial tumor suppressor and a potential diagnostic predictor in TNBC, operating in part through the ITGAV-mediated pathway.

Indexed as

Biomarkers, TumorEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticMicroRNAsTriple Negative Breast NeoplasmsCase-Control StudiesCell Line, TumorCell MovementCell ProliferationDisease ProgressionFemaleFollow-Up StudiesHumansLymphatic MetastasisMiddle AgedPrognosisBiomarkers, TumorMicroRNAsBiomarkerEMTMicroRNA-563Triple-negative breast cancer

Identifiers

PMID42169120
PMCPMC13464650

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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.