Evidence map›Paper›PMID 41689061›Full record

ArticleCancer cell international2026

Research on EBV-miR-BART17-5p targeted Inhibition of ARID1A expression to regulate nasopharyngeal carcinoma dedifferentiation.

Zhen Wu, Xinxiang Su, Yaping Qin, Junjun Pu, Shengjun Xiao, Xiaoling Zhang

Abstract read
In one paragraph

Article in Cancer cell international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing 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

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Zhen Wu *Department of Pathophysiology, Faculty of Basic Medical Sciences, Guilin Medical University, Guilin, 541199, China.
Xinxiang Su *Guangxi Reproductive Medical Center, the First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
Yaping Qin *Department of Pathology, The Second Affiliated Hospital of Guilin Medical University, Guilin, 541199, China.
Junjun PuGuilin Medical University, Guilin, 541199, China.
Shengjun XiaoDepartment of Pathology, The Second Affiliated Hospital of Guilin Medical University, Guilin, 541199, China. xiaoshengjun@glmc.edu.cn.
Xiaoling ZhangDepartment of Physiology, Faculty of Basic Medical Sciences, Guilin Medical University, Guilin, 541199, China. rose2006@glmc.edu.cn.

Funding

Guangxi Key Research and Development Plan (GuiKe AB24010096)Guangxi Science and Technology Base and Talent Special Project (GuiKe AD24999032)The Basic Scientific Research Ability Improvement Project for Young and Middle-aged Teachers of Guangxi Colleges and Universities No.2024KY0522the National Science Foundation of China No. 82260476
6 · The paper itself

Abstract

objectiveTo investigate the role of EBV-miR-BART17-5p in promoting nasopharyngeal carcinoma (NPC) cell dedifferentiation, and to define the potential mediating function of ARID1A in this oncogenic pathway.

methodsBased on clinical NPC specimens, we analyzed EBV-miR-BART17-5p expression via qRT-PCR and its clinicopathological correlation. In vitro, lentiviral transduction was used to establish stable overexpression models in CNE1/CNE2 cells. Functional assays (CCK-8, colony formation, Transwell, tumor-sphere formation) and molecular analyses (Western blot, qRT-PCR) were performed. The targeting relationship was validated using dual-luciferase reporter assays. Immunohistochemistry assessed ARID1A and differentiation markers expression in tissue microarrays.

resultsEBV-miR-BART17-5p expression was elevated in advanced-stage and undifferentiated NPC tissues and correlated with poor patient prognosis. Functionally, it promoted NPC cell proliferation, migration, invasion, tumor-sphere formation, and induced dedifferentiation and stem-like phenotypes. Mechanistically, EBV-miR-BART17-5p directly targeted and downregulated ARID1A, whose low expression was similarly associated with advanced disease, poor survival, and a dedifferentiated phenotype. Crucially, ARID1A overexpression partially rescued the dedifferentiation effects induced by EBV-miR-BART17-5p.

conclusionThis study reveals that EBV-miR-BART17-5p promotes NPC dedifferentiation and malignant progression by targeting ARID1A, identifying a novel viral miRNA tumor-suppressor axis with therapeutic potential.

Indexed as

DedifferentiationEBV encoded small RNAEBV-miR-BART17-5pNasopharyngeal carcinoma

Identifiers

PMID41689061
PMCPMC13011505

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