Evidence map›Paper›PMID 39183060›Full record

ArticleZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences2024

Decarbromodiphenyl ether exposure promotes migration of triple-negative breast cancer cells through miR-221 in extracellular vesicles.

Mengxiao Jiang, Lizhen Wang, Linming Lu, Youhua Tong, Yanyu Li, Hui Zhi

Abstract read
In one paragraph

Article in Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical 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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1 · What the graph read from it

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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.

Mengxiao JiangDepartment of Pathology, Wannan Medical College, Wuhu 241002, Anhui Province, China. xiaoxiaoxiao203@163.com.
Lizhen WangDepartment of Pathology, Wannan Medical College, Wuhu 241002, Anhui Province, China.
Linming LuDepartment of Pathology, Wannan Medical College, Wuhu 241002, Anhui Province, China.
Youhua TongDepartment of Pathology, Wannan Medical College, Wuhu 241002, Anhui Province, China.
Yanyu LiDepartment of Pathology, Wannan Medical College, Wuhu 241002, Anhui Province, China.
Hui ZhiDepartment of Pathology, Wannan Medical College, Wuhu 241002, Anhui Province, China. zhi_hui01@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the effect of decarbromodiphenyl ether (BDE-209) exposure on the migration ability of triple-negative breast cancer (TNBC) cells and to explore the underlying mechanism.

methodsHuman TNBC MDA-MB-231 cells were divided into blank control group and BDE-209 exposure groups (treated with 0.02, 0.20, 2.00, 20.00 and 200.00 ng/mL BDE-209 in high glucose DMEM). Extracellular vehicles (EVs) secreted by MDA-MB-231 cells were isolated by differential ultracentrifugation. Transmission electron microscopy (SEM), nanoparticle tracking analysis (NTA) and Western blotting were performed to characterize the EVs. The effect of the EVs induced by BDE-209 exposure (EVs-BDE-209) on the migration and invasion of MDA-MB-231 cells was detected by wound-healing assay and Transwell test. qRT-PCR was used to measure the miR-221 level in EVs-BDE-209. The expression of MMP9 in MDA-MB-231 cells was determined by Western blotting.

resultsCompared with the blank control, BDE-209 exposure increased the tumor cell-derived EVs in dose-dependent manner. The MDA-MB-231 cells co-cultured with EVs released by 200.00 ng/mL BDE-209 exposure showed an 86% increase in cell migration rate, a 1.32-fold higher number of membrane-penetrating cells, a 2.71-fold higher expression level of miR-221, and a 1.62-fold higher expression level of MMP9 compared with the blank control group (all

conclusionsBDE-209 exposure may promote metastasis potential of MDA-MB-231 cells via EVs-BDE-209 transmitted miR-221.

Indexed as

Cell MovementExtracellular VesiclesHalogenated Diphenyl EthersMicroRNAsTriple Negative Breast NeoplasmsCell Line, TumorFemaleHumansMatrix Metalloproteinase 9decabromobiphenyl etherHalogenated Diphenyl EthersMatrix Metalloproteinase 9MicroRNAsMIR221, humanMMP9 protein, humanCell migrationDecarbromodiphenyl etherExtracellular vesiclesMatrix metalloprotein 9MicroRNA-221Triple-negative breast cancer

Identifiers

PMID39183060
PMCPMC11375496

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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.