Evidence map›Paper›PMID 40777951›Full record

ArticleAfrican health sciences2024

MiRNA-153 attenuates progression of non-small cell lung cancer through targeting positive regulatory/SET domain 2.

Ji Chen, Shiliang Xie, Miao Feng, Dan Wang

Abstract read
In one paragraph

Article in African health sciences, 2024. 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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0citing papers 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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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ji ChenDepartment of Thoracic Surgery, Huashan Hospital Affiliated to Fudan University, Shanghai, China.
Shiliang XieDepartment of Cardiothoracic Surgery, Shanghai Tongji hospital/Tongji hospital Affiliated to Tongji University, Shanghai, China.
Miao FengDepartment of Thoracic Surgery, Huashan Hospital Affiliated to Fudan University, Shanghai, China.
Dan WangDepartment of Traditional Chinese Medicine, Changzheng Hospital, Naval Medical University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: To explore whether micro ribonucleic acid (miR)-153 regulates positive regulatory/SET domain 2 (PRDM2) in a targeted manner and affects the proliferation and apoptosis of non-small cell lung cancer (NSCLC) A549 cells. Methodology: The expressions of miR-153 and PRDM2 in NSCLC tissues and A549 cells were detected by quantitative real-time polymerase chain reaction (qRT-PCR). TargetScan was utilized to predict miR-153 target genes. Methyl thiazolyl tetrazolium (MTT) and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays were carried out to study the cell proliferation and apoptosis. Western blotting was performed to examine the changes in the proteins in the Janus kinase-signal transducer and activator of transcription (JAK/STAT) signaling pathway following the miR-153 overexpression. Results: The expression of miR-153 was decreased and that of PRDM2 was increased in NSCLC tissues and cells. Target genes regulated by miR-153 participated in self-vascular development, miRNA metabolic process and the Wnt signaling pathway. The overexpression of miR-153 led to an obvious reduction in the proliferation ability of A549 cells, a notable increase in apoptotic cells, and significant decreases in phosphorylated (p)-JAK2 and p-STAT3 proteins. Dual-luciferase reporter gene assay revealed that miR-153 could directly modulate the expression level of PRDM2. Conclusion: MiR-153 directly targets PRDM2 and affects A549 cell proliferation and apoptosis through the JAK/STAT pathway.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMicroRNAsTranscription FactorsA549 CellsApoptosisCell ProliferationDisease ProgressionGene Expression Regulation, NeoplasticHumansSignal TransductionMicroRNAsMIRN153 microRNA, humanTranscription FactorsJanus kinase-signal transducer and activator of transcription (JAK/STAT) signaling pathwaymiR-153Non-small cell lung cancerpositive regulatory/SET domain 2

Identifiers

PMID40777951
PMCPMC12327139

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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.