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Updated: Dec 26, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Circular RNA has_circ_0003204 inhibits oxLDL-induced vascular endothelial cell proliferation and angiogenesis
Huifang Liu1, Xirui Ma1, Ziming Mao1
1Department of Endocrinology and Metabolism, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Insights
Circular RNAs (circRNAs) are crucial in atherosclerosis. This study shows hsa_circ_0003204 promotes endothelial cell damage, suggesting it
Area of Science:
- Molecular Biology
- Cardiovascular Research
- Cell Biology
Background:
- Circular RNAs (circRNAs) are prevalent in eukaryotes and implicated in atherosclerosis.
- Endothelial cell dysfunction is central to atherosclerotic plaque development.
Purpose of the Study:
- To investigate the role of hsa_circ_0003204 in atherosclerosis.
- To explore the functional impact of hsa_circ_0003204 on human umbilical vein endothelial cells (HUVECs) under ox-LDL stimulation.
Main Methods:
- Investigated hsa_circ_0003204 expression in ox-LDL-induced HUVECs.
- Performed knockdown of hsa_circ_0003204 to assess its effects.
- Analyzed cell proliferation, migration, invasion, and apoptosis.
- Examined the expression of key endothelial-mesenchymal transition markers (E-cadherin, N-cadherin, vimentin).
Main Results:
- hsa_circ_0003204 was overexpressed in ox-LDL-treated HUVECs.
- Knockdown of hsa_circ_0003204 enhanced HUVEC proliferation, migration, and invasion.
- hsa_circ_0003204 knockdown reduced ox-LDL-induced HUVEC apoptosis.
- Reduced E-cadherin and increased N-cadherin and vimentin expression were observed upon hsa_circ_0003204 knockdown.
Conclusions:
- hsa_circ_0003204 significantly impacts HUVEC proliferation and angiogenesis.
- hsa_circ_0003204 is implicated in endothelial cell damage during atherosclerosis.
- hsa_circ_0003204 represents a potential therapeutic target for atherosclerosis-related endothelial dysfunction.
Abstract:
Circular RNAs (circRNAs) are widely expressed in eukaryotic cells and play a key role in atherosclerosis. The aim of this study is to explore the relationship between hsa_circ_0003204 and atherosclerosis. Here, hsa_circ_0003204 was aberrantly overexpressed in the ox-LDL-induced human umbilical vein endothelial cells (HUVECs). Knockdown of hsa_circ_0003204 facilitated the proliferation, migration, and invasion but reduced the apoptosis of oxLDL-induced HUVECs. Furthermore, hsa_circ_0003204 knockdown significantly reduced the E-cadherin expression but increased the expressions of N-cadherin and vimentin in oxLDL-induced HUVECs. Collectively, these findings suggest that hsa_circ_0003204 plays an important role in the proliferation and angiogenesis of HUVECs, providing a potential target for treating endothelial cell damage in atherosclerosis.
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