Evidence map›Paper›PMID 42576488›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2026

[Overexpression of miR-183-5p enhances malignant phenotype and inhibits ferroptosis of triple-negative breast cancer cells by negatively regulating KLHL24].

Kun Wang, Shunfu Hou, Yong Li, Qinghua Liu, Chonggao Yin, Hongli Li

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Kun WangMedical Research Center, Shandong Second Medical University, Weifang 261053, China.
Shunfu HouDepartment of Clinical Pathology, Shandong Second Medical University, Weifang 261053, China.
Yong LiMedical Research Center, Shandong Second Medical University, Weifang 261053, China.
Qinghua LiuHuman Anatomy Teaching and Research Section, Shandong Second Medical University, Weifang 261053, China.
Chonggao YinCollege of Nursing, Shandong Second Medical University, Weifang 261053, China.
Hongli LiMedical Research Center, Shandong Second Medical University, Weifang 261053, China.

Funding

National Natural Science Foundation of China 82373043
6 · The paper itself

Abstract

objectivesTo investigate the effects of miR-183-5p overexpression on proliferation, invasion, migration, and ferroptosis of triple-negative breast cancer (TNBC) cells and the role of Kelch-like protein 24 (KLHL24) in mediating these effects.

methodsBioinformatics analyses were conducted to screen differentially expressed genes in breast cancer (BRCA) and predict the target gene of miR-183-5p. RT-qPCR was used to verify miR-183-5p expression in normal breast epithelial and TNBC cell lines. Dual-luciferase reporter assay was performed to confirm direct binding of miR-183-5p to 3'-UTR of KLHL24. Western blotting was used to detect KLHL24 expression in different TNBC cells after transfection with miR-183-5p-overexpressing plasmids. MDA-MB-231 cells were co-transfected with NC-miR and NC-KLHL24, oe-miR-183-5p and NC-KLHL24, NC-miR and oe-KLHL24, or oe-miR-183-5p and oe-KLHL24 plasmids, and the changes in cell proliferation, migration and invasion were examined using EdU, Transwell, and wound healing assays. Western blotting was used to detect the changes in expressions of ferroptosis-related proteins (GPX4, SLC7A11, and Nrf2), and ROS, LPO, MDA, and GSH levels in the transfected cells were determined.

resultsThe expression of miR-183-5p was significantly elevated in BRCA tissues and TNBC cell lines, and MDA-MB-231 cells showed the highest miR-183-5p expression. Dual-luciferase reporter assay confirmed the direct binding of miR-183-5p to 3'-UTR of KLHL24. Overexpression of miR-183-5p significantly downregulated KLHL24 expression. In TNBC cells, miR-183-5p overexpression obviously promoted cell proliferation, invasion, and migration, upregulated the expressions of GPX4, SLC7A11 and Nrf2, reduced the levels of ROS, LPO and MDA, and increased the level of GSH (

conclusionsOverexpression of miR-183-5p enhances TNBC cell proliferation, invasion, migration and inhibits ferroptosis by negatively regulating KLHL24.

Indexed as

FerroptosisMicroRNAsTriple Negative Breast NeoplasmsAmino Acid Transport System y+Cell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMDA-MB-231 CellsNeoplasm InvasivenessAmino Acid Transport System y+MicroRNAsMIRN183 microRNA, humanSLC7A11 protein, humanferroptosisinvasion and migrationKLHL24miR-183-5pproliferationtriple-negative breast cancer

Identifiers

PMID42576488
PMCPMC13458494

What Socratic holds

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Registered trials

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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 Socratic graph.