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Updated: Jan 9, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
CircFOXK2 induces non-small cell lung cancer tumorigenesis through the miR-328-5p/PKP3 axis
Tongwei Xiang1, Liping Chen2, Huaying Wang3
1Department of Respiratory and Critical Care Medicine, Yinzhou People's Hospital, The Affiliated People's Hospital of Ningbo University, Ningbo, China. 603358673@qq.com.
Abstract:
Circular RNAs (circRNAs) are non-coding RNAs (ncRNAs) implicated in the onset and advancement of various human cancers. Among these, circFOXK2 has been linked to non-small cell lung cancer (NSCLC); however, its precise functions and underlying molecular mechanisms are not fully understood. This study shows the first experimental findings that circFOXK2 promotes NSCLC tumor progression by modulating the miR-328-5p/PKP3 signaling pathway. Levels of circFOXK2, miR-328-5p, and PKP3 were evaluated by qRT-PCR. Cellular (NSCLSC) proliferation was examined via CCK-8 assays, migratory capacity via wound healing, and invasive potential via Transwell assays. Potential binding interactions between miR-328-5p and circFOXK2 were first assessed using bioinformatic analysis and verified using a dual-luciferase reporter assay (DLRGAs). Regulatory relationships among circFOXK2, miR-328-5p, and PKP3 were further investigated through qRT-PCR analysis. Elevated expression of circFOXK2 and reduced levels of miR-328-5p were observed in NSCLC cell lines and tissues. Functionally, circFOXK2 enhanced cellular propagation, dissemination, and invasion in vitro. Mechanistic evaluation revealed that circFOXK2 upregulates PKP3 by acting as an miR-328-5p sponge. The findings demonstrate that circFOXK2 contributes to NSCLC tumorigenesis via modulation of the miR-328-5p/PKP3 pathway, identifying this signaling axis as a potential therapeutic target in NSCLC.
Insights
Circular RNAs (circRNAs) promote non-small cell lung cancer (NSCLC) progression. This study reveals circFOXK2 enhances NSCLC by sponging miR-328-5p, upregulating PKP3, highlighting a novel therapeutic pathway.
Area of Science:
- Oncology
- Molecular Biology
- RNA Biology
Background:
- Circular RNAs (circRNAs) are regulatory non-coding RNAs (ncRNAs) involved in cancer development.
- The specific role and molecular mechanisms of circFOXK2 in non-small cell lung cancer (NSCLC) remain largely unelucidated.
Purpose of the Study:
- To investigate the functional role of circFOXK2 in NSCLC progression.
- To elucidate the molecular mechanism by which circFOXK2 influences NSCLC tumorigenesis, focusing on the miR-328-5p/PKP3 signaling pathway.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) to assess expression levels of circFOXK2, miR-328-5p, and PKP3.
- Cellular assays including CCK-8 for proliferation, wound healing for migration, and Transwell assays for invasion.
- Bioinformatic analysis and dual-luciferase reporter assays (DLRGAs) to confirm interactions between miR-328-5p and circFOXK2.
Main Results:
- circFOXK2 and PKP3 were upregulated, while miR-328-5p was downregulated in NSCLC tissues and cell lines.
- circFOXK2 significantly promoted NSCLC cell proliferation, migration, and invasion in vitro.
- circFOXK2 functions as a molecular sponge for miR-328-5p, leading to the upregulation of its target gene, PKP3.
Conclusions:
- circFOXK2 drives NSCLC progression through the miR-328-5p/PKP3 signaling axis.
- This circRNA-mediated pathway represents a potential therapeutic target for non-small cell lung cancer treatment.
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