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Updated: Sep 1, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
CircRNA 0009043 suppresses non-small-cell lung cancer development via targeting the miR-148a-3p/DNAJB4 axis
Kelin She1,2, Shaoqi Yu3, Shushuai He3
1Department of Thoracic Surgery, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Nomal University, Changsha, Hunan, 410005, China. shekelin@163.com.
Background:
Circular RNAs (circRNAs) are important regulators of the development and progression of non-small-cell lung cancer (NSCLC) and many other malignancies. The functional importance of circ_0009043 in NSCLC, however, has yet to be established.
Methods:
The expression of circ_0009043, miR-148a-3p, and DnaJ heat shock protein family (Hsp40) member B4 (DNAJB4) in NSCLC cells was assessed via qPCR. The proliferative activity of these cells was examined through EdU uptake and CCK-8 assays, while flow cytometry approaches were used to examine apoptotic cell death rates. Protein expression was measured through Western immunoblotting. Interactions between miR-148a-3p and circ_0009043 or DNAJB4 were detected through RNA immunoprecipitation (RIP) and dual-luciferase reporter assays. The in vivo importance of circ_0009043 as a regulator of oncogenic activity was assessed using murine xenograft models.
Results:
Both NSCLC cells and tissue samples were found to exhibit circ_0009043 upregulation, and lower circ_0009043 expression levels were found to be related to poorer NSCLC patient overall survival. Knocking down circ_0009043 resulted in the enhancement of NSCLC cell proliferative activity and the suppression of apoptotic tumor cell death in vitro, while also driving more rapid in vivo tumorigenesis. Mechanistically, circ_0009043 was found to function as a molecular sponge that sequestered miR-148a-3p, which was in turn able to directly suppress DNAJB4 expression. When miR-148a-3p was overexpressed, this reversed the impact of knocking down circ_0009043 on the apoptotic death and proliferation of NSCLC cells. Conversely, miR-148a-3p inhibition resulted in the suppression of NSCLC cell apoptosis and the enhancement of tumor cell growth, while the downregulation of DNAJB4 reversed these changes.
Conclusion:
Circ_0009043 acts as a tumor suppressor in NSCLC cells, promoting DNAJB4 upregulation via the sequestration of miR-148a-3p.
Insights
Circular RNA (circRNA) circ_0009043 suppresses non-small-cell lung cancer (NSCLC) by sponging miR-148a-3p, leading to increased DNAJB4 expression and promoting tumor cell apoptosis.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Circular RNAs (circRNAs) are critical in cancer development, but circ_0009043's role in non-small-cell lung cancer (NSCLC) remains unclear.
- Understanding circRNA functions is vital for developing novel cancer therapies.
Purpose of the Study:
- To investigate the functional role and molecular mechanism of circ_0009043 in NSCLC.
- To determine the relationship between circ_0009043, miR-148a-3p, and DNAJB4 in NSCLC progression.
Main Methods:
- Quantitative PCR (qPCR) and Western immunoblotting assessed gene and protein expression.
- Cell proliferation, apoptosis, and in vivo tumor growth were evaluated using EdU, CCK-8, flow cytometry, and murine xenograft models.
- RNA immunoprecipitation (RIP) and dual-luciferase reporter assays elucidated molecular interactions.
Main Results:
- Circ_0009043 was upregulated in NSCLC, with lower levels correlating with poorer survival.
- Circ_0009043 knockdown enhanced proliferation and inhibited apoptosis in NSCLC cells, promoting tumor growth in vivo.
- Circ_0009043 acts as a sponge for miR-148a-3p, inhibiting its ability to suppress DNAJB4 expression.
Conclusions:
- Circ_0009043 functions as a tumor suppressor in NSCLC.
- The circ_0009043/miR-148a-3p/DNAJB4 axis regulates NSCLC cell proliferation and apoptosis.
- Targeting circ_0009043 may offer a therapeutic strategy for NSCLC.
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