Evidence map›Paper›PMID 42337672›Full record

ArticleWorld journal of surgical oncology2026

LncRNA ACTA2-AS1 acts as a bladder cancer prognostic biomarker and blocks malignant advance via miR-148b-3p/DNAJB4.

Xing Chen, Qunfu Tang, Yingjie Wang, Jianbin Zhang, Lei Zhou

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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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xing Chen *Department of Urology, China-Japan Friendship Hospital, Beijing, 100029, China.
Qunfu Tang *Department of Urology, Liwan Central Hospital of Guangzhou, Guangzhou, 510380, China.
Yingjie WangDepartment of Oncology, Tongxiang First People's Hospital, Jiaxing, Zhejiang Province, 314500, People's Republic of China.
Jianbin ZhangDepartment of Urology, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, 030001, China.
Lei ZhouDepartment of Urology, Central Hospital Affiliated to Shandong First Medical University, No.105 Jiefang Road, Lixia District, Jinan, 250013, China. zhouleizhll@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong non-coding RNA (lncRNA) is crucial in bladder cancer (BCa) development. This research explores the clinical significance and underlying mechanisms of lncRNA ACTA2-AS1 in BCa.

methodsFrom the GEO database, differentially expressed lncRNAs (DElncRNAs) in BCa were identified, and tumor, along with adjacent non-tumor tissue samples from 132 patients, were collected. RT-qPCR was employed for the quantitative measurement of ACTA2-AS1, miR-148b-3p, and DNAJB4 expression. Chi-square analysis was employed to assess the association of ACTA2-AS1 with clinical features. Kaplan-Meier and Cox regression evaluated ACTA2-AS1's prognostic value. CCK-8, Transwell, and flow cytometry assays evaluated cell proliferation, migration, invasion, apoptosis, and cell cycle arrest. DLR and RIP tests confirmed miR-148b-3p's targeting of ACTA2-AS1 and DNAJB4.

resultsACTA2-AS1 showed significant downregulation in four GEO databases. Moreover, both ACTA2-AS1 and DNAJB4 were notably decreased in BCa tumor tissues, while miR-148b-3p increased significantly. Low ACTA2-AS1 expression correlates with poor tumor differentiation, positive lymph node metastasis, and TNM stage III-IV. Moreover, patients with low ACTA2-AS1 expression are associated with a significantly unfavorable prognosis. Mechanistically, miR-148b-3p targets ACTA2-AS1 and DNAJB4. The suppression impacts of ACTA2-AS1 on BCa cell proliferation, migration, and invasion, and its boost of apoptosis and cell cycle arrest were greatly reversed by miR-148b-3p.

conclusionLow ACTA2-AS1 expression is a potential biomarker for unfavorable prognosis in BCa patients. Furthermore, ACTA2-AS1 may counteract BCa's malignant biological behaviors via targeting the miR-148b-3p/DNAJB4 axis.

Indexed as

Biomarkers, TumorGene Expression Regulation, NeoplasticHSP40 Heat-Shock ProteinsMicroRNAsRNA, Long NoncodingUrinary Bladder NeoplasmsActinsApoptosisCell Line, TumorCell MovementCell ProliferationFemaleFollow-Up StudiesHumansMaleMiddle AgedACTA2 protein, humanActinsBiomarkers, TumorHSP40 Heat-Shock ProteinsMicroRNAsMIRN148 microRNA, humanRNA, Long NoncodingACTA2-AS1Bladder cancerDNAJB4miR-148b-3pPrognostic

Identifiers

PMID42337672
PMCPMC13543625

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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.