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Updated: Sep 29, 2025

In Vivo Nanovector Delivery of a Heart-specific MicroRNA-sponge
Published on: June 15, 2018
Circular RNA circ_0001006 aggravates cardiac hypertrophy via miR-214-3p/PAK6 axis
Xuefeng Lin1,2,3,4,5,6, Liqin Zhang6, Wei Zhang7
1Department of Cardiovascular Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shanxi 710061, PR China.
Insights
Circular RNA hsa_circ_0001006 (circ_0001006) worsens cardiac hypertrophy by inhibiting miR-214-3p, which increases PAK6 levels. This finding reveals a novel mechanism in heart disease progression.
Area of Science:
- Molecular Biology
- Genetics
- Cardiovascular Research
Background:
- Circular RNAs (circRNAs) regulate gene expression in various biological processes.
- The specific role of circRNAs in the development of heart disease remains largely unexplored.
- Cardiac hypertrophy is a significant risk factor for heart failure.
Purpose of the Study:
- To investigate the role and underlying mechanism of circRNAs in cardiac hypertrophy.
- To identify specific circRNAs involved in the pathological process of cardiac hypertrophy.
Main Methods:
- Upregulation of circRNA hsa_circ_0001006 (circ_0001006) was observed in cardiac hypertrophy models.
- Gain-of-function and knockdown experiments demonstrated circ_0001006's role in cardiomyocyte hypertrophy.
- RNA pull-down and dual-luciferase reporter assays were used to elucidate molecular interactions.
Main Results:
- circ_0001006 was upregulated in cardiac hypertrophy and induced hypertrophy in cardiomyocytes.
- Knockdown of circ_0001006 alleviated angiotensin II-induced cardiomyocyte hypertrophy.
- circ_0001006 directly binds to miR-214-3p and inhibits its function.
- miR-214-3p targets the PAK6 gene, and circ_0001006 blocks this interaction.
Conclusions:
- circRNA_0001006 exacerbates cardiac hypertrophy.
- The mechanism involves the suppression of miR-214-3p, leading to increased PAK6 expression.
- circ_0001006 represents a potential therapeutic target for cardiac hypertrophy.
Aim:
Circular RNAs (circRNAs) control gene expression in a series of physiological and pathological processes, but their role in heart disease is unknown. This research illustrates the role and potential mechanism of circRNA in cardiac hypertrophy.
Methods And Results:
In this report, we found that circular RNA hsa_circ_0001006 (circ_0001006) was upregulated in cardiac hypertrophy mice and cardiomyocytes treated with angiotensin II (Ang II). Next, we noticed that gain of function circ_0001006 could induce cardiomyocyte hypertrophy; oppositely, knockdown of circ_0001006 remitted Ang II-induced cardiomyocyte hypertrophy. Biotin-coupled miRNA and RNA-pull down assays showed that miR-214-3p could bind with circ_0001006 and gain the function of miR-214-3p abrogated the pro-hypertrophy effect of circ_0001006. Furthermore, Further, dual-luciferase reporter assay showed that miR-214-3p could interact with 3'UTRs of the PAK6 gene, and circRNA_0001006 could block the above interactions. Additionally, PAK6 expression is inhibited by miR-214-3p mimic in cardiomyocytes but enhanced by over-expression of circRNA_000203 in vitro.
Conclusions:
Our data demonstrated that circRNA_0001006 exacerbates cardiac hypertrophy via suppressing miR-214-3p leading to enhanced PAK6 levels.
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