Evidence map›Paper›PMID 41358261›Full record

ArticleBreast cancer (Dove Medical Press)2025

Circular RNA DENND4C Regulates Cell Malignant Behaviors in Breast Cancer Through the miR-26a-5p/HSPA8 Axis.

MeiYan Guo, Yan Chang, YuNa Dai, Xia Liu, SuFang Shi, JuMei Li, WeiGuang Liu, JianJun Han

Abstract read
In one paragraph

Article in Breast cancer (Dove Medical Press), 2025. 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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2 · The registry

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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

8 authors.

MeiYan Guo *Department of Breast Surgery, Affiliated Hospital of Hebei Engineering University, Handan City, Hebei Province, 056002, People's Republic of China.
Yan Chang *Department of Breast Surgery, Affiliated Hospital of Hebei Engineering University, Handan City, Hebei Province, 056002, People's Republic of China.
YuNa DaiDepartment of Breast Surgery, Affiliated Hospital of Hebei Engineering University, Handan City, Hebei Province, 056002, People's Republic of China.
Xia LiuDepartment of Health Examination, Affiliated Hospital of Hebei Engineering University, Handan City, Hebei Province, 056002, People's Republic of China.
SuFang ShiDepartment of Breast Surgery, Affiliated Hospital of Hebei Engineering University, Handan City, Hebei Province, 056002, People's Republic of China.
JuMei LiDepartment of Breast Surgery, Affiliated Hospital of Hebei Engineering University, Handan City, Hebei Province, 056002, People's Republic of China.
WeiGuang LiuDepartment of Breast Surgery, Yangzhou Maternal and Child Health Hospital, Yangzhou City, Jiangsu Province, 225007, People's Republic of China.
JianJun HanDepartment of Breast Surgery, Affiliated Hospital of Hebei Engineering University, Handan City, Hebei Province, 056002, People's Republic of China.ORCID 0009-0003-3858-4603

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: At present, the potential functions of most circRNAs in breast cancer (BC) have not been fully elucidated. The investigatory research planned to study biological function of circDENND4C in BC and reveal its downstream molecular mechanism. Methods: A total of fifty pairs of BC tissue and their corresponding normal tissue were obtained. circDENND4C/miR-26a-5p/Human 71 kDa heat shock cognate protein (HSPA8) were assessed through RT-qPCR or Western blot. After transfecting the relevant plasmids, MKN-45 cell proliferation, cell cycle, invasion, and migration were assessed through MTT and colony formation assays, flow cytometry, and Transwell tests. Bioinformatics analysis, RIP and dual luciferase reporting experiments verified the interaction between circDENND4C, miR-26a-5p, and HSPA8. Results: Increased circDENND4C was found in BC and was related to a poor prognosis in BC patients. HSPA8 was upregulated and miR-26a-5p was downregulated in BC. Functionally, silencing circDENND4C prevented cells from proliferation, invasion, and migration, and induced cell cycle arrest at G0/G1 phase. circDENND4C overexpression had the opposite effect. The effects of circDENND4C overexpression or knockdown in BC cells were counteracted by overexpressing miR-26a-5p or HSPA8, respectively. circDENND4C mediated HSPA8 expression by competitively adsorbing miR-26a-5p. Conclusion: circDENND4C absorbs miR-26a-5p to target HSPA8, thereby promoting BC progression, which provides a new insight into the mechanism of BC.

Indexed as

breast cancercircDENND4CHSPA8miR-26a-5p

Identifiers

PMID41358261
PMCPMC12681268

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