Evidence map›Paper›PMID 42178363›Full record

ArticleScientific reports2026

m6A modification-mediated lncRNA UNC5B-AS1 enhances HCC progression through miR-760/IL6 axis.

Li-Ping Yu, Sheng-Yu Huang, Kun-Peng Li, Jun-Sheng Ni, Zhi-Ping Huang, Zhou-Feng Deng

Abstract read
In one paragraph

Article in Scientific reports, 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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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

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Li-Ping Yu *Department of Oncology, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, 1111, Xianxia Road, Shanghai, 200336, China.
Sheng-Yu Huang *Department of Hepato-Pancreato-Biliary Surgery, School of Medicine, Shanghai Tenth People's Hospital, Tongji University, Shanghai, 200072, China.
Kun-Peng Li *Department of Hepato-Pancreato-Biliary Surgery, School of Medicine, Shanghai Fourth People's Hospital, Tongji University, Shanghai, 200434, China. doctorkpl@163.com.
Jun-Sheng NiSchool of Medicine, Yangpu Hospital, Tongji University, Shanghai, 200090, China. China.nijs77@me.com.
Zhi-Ping HuangDepartment of Hepato-Pancreato-Biliary Surgery, General Hospital of Southern Theater Command, Guangzhou, 315000, China. China.surg411@163.com.
Zhou-Feng DengDepartment of Oncology, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, 1111, Xianxia Road, Shanghai, 200336, China. 99420230@qq.com.

Funding

ake-off Program No. TF2024YZZY03Clinical Research Cultivation Programa No.2023LC004Guangzhou Science and Technology plan 2025A04J3674
6 · The paper itself

Abstract

WT1-associated protein (WTAP)-catalyzed m6A methylation drives oncogenic processes in HCC. Long noncoding RNA UNC5B-AS1 are associated with various types of cancer including hepatocellular carcinoma (HCC). Previous study indicated that UNC5B-AS1 promotes HCC progression. However, the precise roles of WTAP/UNC5B-AS1 axis in HCC progression remain unclear. In this study, we found that the m6A modification sites are highly abundant on UNC5B-AS1, and methylase WTAP enhances UNC5B-AS1 stability through m6A reader-YTHDF1 and up-regulates its expression in HCC. Functional tests showed that WTAP/UNC5B-AS1 axis drives HCC progression. Mechanically, UNC5B-AS1 acts as a molecular sponge to hsa-miR-760, to up-regulate the expression of Interleukin-6 (IL6), and plays a role in enhancing HCC progression. Our study reveals a mechanism by which m6A-RNA regulates oncogene activity, which might result in the creation of a therapeutic strategy for the treatment of HCC.

Indexed as

Carcinoma, HepatocellularCell Cycle ProteinsInterleukin-6Liver NeoplasmsMicroRNAsNetrin ReceptorsRNA, Long NoncodingRNA Splicing FactorsAdenosineCell Line, TumorDisease ProgressionGene Expression Regulation, NeoplasticHumansRNA MethylationAdenosineCell Cycle ProteinsInterleukin-6MicroRNAsNetrin ReceptorsN-methyladenosineRNA, Long NoncodingRNA Splicing FactorsUNC5B protein, humanWTAP protein, humanHepatocellular carcinoma (HCC)IL6N6-methyladenosineUNC5B-AS1WTAP

Identifiers

PMID42178363
PMCPMC13462090

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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.