Evidence map›Paper›PMID 36911385›Full record

ArticleExperimental and therapeutic medicine2023

A20 affects macrophage polarization through the NLRP3 inflammasome signaling pathway and promotes breast cancer progression.

Yanbin Zheng, Shenglan Wang, Yutong Zhong, Chunhong Huang, Xinjie Wu

Abstract read
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Article in Experimental and therapeutic medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yanbin ZhengDepartment of Clinical Laboratory, LongYan First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 364000, P.R. China.
Shenglan WangDepartment of Clinical Laboratory, LongYan First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 364000, P.R. China.
Yutong ZhongDepartment of Clinical Laboratory, LongYan First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 364000, P.R. China.
Chunhong HuangDepartment of Clinical Laboratory, LongYan First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 364000, P.R. China.
Xinjie WuDepartment of Emergency, LongYan First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian 364000, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common malignant tumor in females, and the majority of patients succumb to metastasis. The present study aimed to investigate the association between tumor necrosis factor alpha-induced protein 3 (A20), NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) and tumor-associated macrophage polarization, and their effects on the proliferation and metastasis of breast cancer cells. The expression of A20 in breast cancer cells was analyzed by reverse transcription-quantitative PCR (RT-qPCR) and western blotting. RT-qPCR and western blotting were also used to confirm the transfection efficiency. The viability, clone formation, migration, invasion and angiogenesis of transfected breast cancer cells were detected by Cell Counting Kit-8, colony formation, wound healing, Transwell and tube formation assays, respectively. Activated macrophages, namely M1 and M2 type macrophages, were observed by double staining immunofluorescence. The levels of M1 and M2 macrophage markers were analyzed by qPCR. The expression of angiogenesis-related proteins and NLRP3 inflammasome activation-associated proteins was detected by western blotting. The results revealed that A20 was highly expressed in breast cancer cells. Interference with A20 inhibited the proliferation, invasion, migration and angiogenesis of breast cancer cells, and inhibited the M2-like polarization of macrophages. Interference with A20 promoted the activation of the NLRP3 inflammasome. The NLRP3 inhibitor MCC950 alleviated the effect of interference with A20 to promote macrophage proliferation and recruitment, as well as M2-like polarization. In conclusion, interference with A20 inhibited macrophage proliferation and M2-like polarization through the NLRP3 inflammasome signaling pathway to inhibit breast cancer progression.

Indexed as

A20 (tumor necrosis factor alpha-induced protein 3)breast cancerLRR- and pyrin domain-containing protein 3 inflammasomemacrophage polarityNOD-

Identifiers

PMID36911385
PMCPMC9995841

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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.