Circular RNA dehydrodolichyl diphosphate synthase facilitated triple‐negative breast cancer progression via miR‐362‐3p/DDX5 axis. Issue 6 (28th March 2022)

• Record Type: Journal Article
• Authors: Cui, Suping; Zhang, Yong; Xing, Li; Li, Rui; Piao, Yingshi; Liu, Honggang
• Is Part Of: Environmental toxicology. Volume 37:Issue 6(2022)
• Page Start: 1483
• Page End: 1494
• Publication Date: 2022-03-28
• Subjects: circDHDDS -- DDX5 -- miR‐362‐3p -- triple‐negative breast cancer; Water quality bioassay -- Periodicals; Water -- Pollution -- Toxicology -- Periodicals; Microbiological assay -- Periodicals; Toxicity testing -- Periodicals; Environmental toxicology -- Periodicals; Environmental Pollution -- Periodicals; Environmental Pollutants -- Periodicals; Environmental Monitoring -- Periodicals; Écotoxicologie -- Périodiques; Pollution -- Périodiques; 615.902
• DOI: 10.1002/tox.23500
• Languages: English
• ISSNs: 1520-4081

Abstract

Abstract: Background: Triple‐negative breast cancer (TNBC) is a common hypotype of breast cancer. Circular RNAs (circRNAs) are burgeoning serve as vital controllers in numerous tumors. Nevertheless, the expression and regulatory mode of circRNAs in TNBC are still indistinct. This paper aimed to reveal the function and molecular mechanism of circular RNA dehydrodolichyl diphosphate synthase (circDHDDS) in TNBC. Methods: The contents of circDHDDS, DHDDS mRNA, microRNA‐362‐3p (miR‐362‐3p) and DEAD (Asp‐Glu‐Ala‐Asp) box polypeptide 5 (DDX5) were indicated by quantitative real‐time polymerase chain reaction (qRT‐PCR) and western blot. The colony formation assay and 5‐ethynyl‐2'‐deoxyuridine (EdU) assay were executed to assess cell proliferation. The flow cytometry assay was utilized to detect cell apoptosis. The transwell assay and tube formation assay were applied to measure cell migration, invasion and angiogenesis. The targeted relationships of miR‐362‐3p and circDHDDS or DDX5 were forecasted and detected by dual‐luciferase reporter assay. The in vivo test was implemented to confirm the effect of circDHDDS. Results: The contents of circDHDDS and DDX5 were increased, and miR‐362‐3p level was decreased in TNBC. CircDHDDS deficiency reserved cell proliferation, migration, invasion and angiogenesis, while facilitated cell apoptosis in TNBC cells. Furthermore, miR‐362‐3p was validated to exert a tumor repressive effect in TNBC cells by suppressing DDX5. Moreover, DDX5 could regulate the development of TNBC. The experimental data exposed that levels of miR‐362‐3p presented noteworthy negative correlation with circDHDDS and DDX5, while circDHDDS and DDX5 exhibited significant positive correlation. In mechanism, circDHDDS bound to miR‐362‐3p to modulate DDX5 expression. In addition, circDHDDS knock‐down also attenuated tumor growth. Conclusion: CircDHDDS expedited TNBC by swelling DDX5 via adapting miR‐362‐3p.