Evidence map›Paper›PMID 40072551›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2025

Long noncoding RNA MATN1-AS1 contributes to oxaliplatin resistance of gastric cancer cells through miR-518b/ZNF281 axis.

Xiuhuan Qiu, Licheng Zhang, Fengying Guo, Ruixiang Guo

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 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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5 · Who and what money

Authors and funding

4 authors.

Xiuhuan Qiu *Outpatient, Zhongshan Hospital, Xiamen University, Xiamen, 361004, China.
Licheng Zhang *Anesthesia Resuscitation Room, Zhongshan Hospital, Xiamen University, Xiamen, 361004, China.
Fengying GuoDepartment of Tumor Radiotherapy, Zhongshan Hospital, Xiamen University, Xiamen, 361004, China. guofengying126@hotmail.com.
Ruixiang GuoDepartment of Tumor Radiotherapy, Zhongshan Hospital, Xiamen University, Xiamen, 361004, China. harrison1314@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemoresistance leads to poor outcomes of patients with gastric cancer (GC). Long non-coding RNAs (lncRNAs) have been demonstrated as novel gene modulators in various carcinomas and chemoresistance. Our study aimed to investigate the role and underlying modulatory mechanism of lncRNA MATN1-AS1 in GC chemoresistance. CCK-8, flow cytometry, and Transwell assays were performed to explore the influence of the MATN1-AS1/microRNA (miR)-518b/zinc finger protein 281 (ZNF281) axis on the half inhibition concentration (IC50) to oxaliplatin (OXA), apoptosis, migration, and invasion of OXA-resistant GC cells. Dual-luciferase reporter assay was conducted to confirm the target association between miR-518b and MATN1-AS1 (or ZNF281). Xenograft mouse models were established to confirm the role of MATN1-AS1 silencing in vivo. The expression of MATN1-AS1, miR-518b, ZNF281, and multidrug resistance-related genes was detected through RT-qPCR and western blotting. MATN1-AS1 expression was upregulated in OXA-resistant GC tissues and cell lines versus OXA-sensitive tissues and parental cell lines. MATN1-AS1 depletion significantly inhibited the IC50 value of OXA, cell migration, invasion, and drug resistance but promoted cell apoptosis in OXA-resistant GC cells. Additionally, MATN1-AS1 upregulated ZNF281 expression by sponging miR-518b in OXA-resistant GC cells. Inhibiting miR-518b or overexpressing ZNF281 antagonized the effects of MATN1-AS1 silencing on OXA resistance of GC cells. Upregulation of ZNF281 abrogated the suppressive effects of miR-518b overexpression on OXA resistance of GC cells. Moreover, MATN1-AS1 knockdown suppressed tumor growth, OXA resistance, and Ki-67 expression in xenograft mouse models. MATN1-AS1 promotes OXA resistance of GC cells by enhancing ZNF281 expression via sequestration of miR-518b, shedding new light on the chemoresistance of GC.

Indexed as

Antineoplastic AgentsDrug Resistance, NeoplasmMicroRNAsOxaliplatinRepressor ProteinsRNA, Long NoncodingStomach NeoplasmsAnimalsApoptosisCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticHumansMaleMiceAntineoplastic AgentsMicroRNAsMIRN508 microRNA, humanOxaliplatinRepressor ProteinsRNA, Long NoncodingGastric cancerMATN1 antisense RNA 1miR-518bOxaliplatin resistanceZinc finger protein 281

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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.