Evidence map›Paper›PMID 40660060›Full record

ArticleMolecular biology reports2025

Silencing lncRNA MCM3AP-AS1 protects against cisplatin-induced cell death in A549 lung cancer cells.

Ibrahim Bozgeyik, Demet Tasdemir, Esra Bozgeyik, Haydar Bagis, Serdar Oztuzcu, Ahmet Ferudun Isik

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Article in Molecular biology reports, 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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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

Ibrahim BozgeyikDepartment of Medical Biology, Faculty of Medicine, Adiyaman University, 02040, Adiyaman, Turkey. i.bozgeyik@gmail.com.
Demet TasdemirRespiratory Diseases and Respiratory Surgery Research and Practice Center, Gaziantep University, Gaziantep, Turkey.
Esra BozgeyikDepartment of Medical Biology, Faculty of Medicine, Adiyaman University, 02040, Adiyaman, Turkey.
Haydar BagisDepartment of Medical Genetics, Faculty of Medicine, Adiyaman University, Adiyaman, Turkey.
Serdar OztuzcuDepartment of Medical Biology and Genetics, Faculty of Medicine, Gaziantep University, Gaziantep, Turkey.
Ahmet Ferudun IsikRespiratory Diseases and Respiratory Surgery Research and Practice Center, Gaziantep University, Gaziantep, Turkey.

Funding

Adiyaman Üniversitesi,Türkiye TIPFMAP/2023-0004
6 · The paper itself

Abstract

backgroundLung cancer remains the leading cause of cancer-related mortality worldwide, largely due to the development of resistance to standard chemotherapeutic agents such as cisplatin. Recent evidence has highlighted the regulatory role of long non-coding RNAs (lncRNAs) in mediating drug resistance mechanisms. In this study, we aimed to reveal the role of MCM3AP-AS1 in cisplatin-induced cell death in lung cancer cells. METHODS AND

resultsAs a result, we found that MCM3AP-AS1, a lncRNA previously associated with poor prognosis in various cancers, was significantly upregulated in A549 lung cancer cells following cisplatin treatment. Using RNA interference-mediated silencing of MCM3AP-AS1, we observed a marked increase in cell viability and a decrease in apoptosis, as determined by MTT assay, annexin V/PI flow cytometry, and acridine orange/ethidium bromide staining.

conclusionsThese findings suggest that MCM3AP-AS1 may be a crucial modulator of cisplatin-induced apoptosis in lung cancer cells.

Indexed as

CisplatinLung NeoplasmsRNA, Long NoncodingA549 CellsAcetyltransferasesAntineoplastic AgentsApoptosisCell DeathCell Line, TumorCell ProliferationCell SurvivalDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsAcetyltransferasesAntineoplastic AgentsCisplatinIntracellular Signaling Peptides and ProteinsMCM3AP protein, humanRNA, Long NoncodingCancerCisplatinLncRNALung cancerMCM3AP-AS1

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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.