Evidence map›Paper›PMID 40751520›Full record

ArticleArchives of Iranian medicine2025

Synergistic Effect of miR-383 and Cisplatin on Inhibition of Growth, Proliferation, and Migration of Lung Cancer Cells.

Vagef Elyaszadeh, Maryam Tohidast, Seyed Samad Hosseini, Mohammad Amini, Parinaz Marami, Behzad Baradaran, Amir Ali Mokhtarzadeh, Asiyeh Jebelli

Abstract read
In one paragraph

Article in Archives of Iranian medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Vagef ElyaszadehDepartment of Biological Science, Faculty of Basic Science, Higher Education Institute of Rab-Rashid, Tabriz, Iran.ORCID 0009-0003-8817-7109
Maryam TohidastImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0003-4673-554X
Seyed Samad HosseiniImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0002-3722-4716
Mohammad AminiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0001-7543-9577
Parinaz MaramiDepartment of Biological Science, Faculty of Basic Science, Higher Education Institute of Rab-Rashid, Tabriz, Iran.ORCID 0009-0006-9115-1729
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0002-8642-6795
Amir Ali MokhtarzadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0002-4515-8675
Asiyeh JebelliDepartment of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.ORCID 0000-0001-9494-2207

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer (LC) is a common life-threatening malignancy in humans. Cisplatin has been widely used in the treatment of various types of cancer. miR-383 is dysregulated in multiple cancers, and participates in tumorigenic processes, including apoptosis, proliferation, metastasis, and drug resistance. This study aimed to investigate the synergistic effect of miR-383 and cisplatin in LC.

methodsA549 cells were treated with cisplatin and miR-383 separately or in combination. Cell viability, apoptosis induction, stemness features, migratory capacity, and autophagy were measured by various methods. In addition, quantitative real-time PCR (qRT-PCR) was used to evaluate the expression levels of genes involved in apoptosis, stemness, and migration.

resultsThe results demonstrated that miR-383 transfection in A549 cells increased their chemosensitivity to cisplatin, enhancing cisplatin-induced apoptosis (from 11.28% to 37.86%). This effect was mediated by regulating key genes such as

conclusionThe findings indicate that the combination treatment of miR-383 and cisplatin suppressed cell proliferation, migration and colony formation while enhancing the sensitivity of A549 cells to chemotherapy compared to monotherapy. These results suggest that miR-383 combination therapy warrants further investigation as a potential strategy for LC treatment.

Indexed as

Antineoplastic AgentsCell ProliferationCisplatinLung NeoplasmsMicroRNAsA549 CellsApoptosisAutophagyCaspase 3Cell MovementCell SurvivalDrug SynergismGene Expression Regulation, NeoplasticHumansAntineoplastic AgentsCaspase 3CisplatinMicroRNAsMIRN383 microRNA, humanApoptosisCisplatinCombination therapyLung cancermiR-383

Identifiers

PMID40751520
PMCPMC12305408

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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.