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LncRNA NEAT1 Promotes the Progression of Gastric Cancer Through Modifying the miR-1224-5p/RSF1 Signaling Axis
Luoluo Yang1, Min Wang2, Ping He1
1Department of Gastroenterology, First Hospital of Jilin University, Changchun 130021, Jilin, People's Republic of China.
Introduction:
The therapy of patients with advanced phase gastric cancer is still a huge threat, with extremely imperfect therapies authorized. Even if the amassed indications have validated the significance of lncRNA in gastric cancer, few understandings are stated concerning nuclear paraspeckle assembly transcript 1 (NEAT1) practical functions and molecular mechanisms.
Methods:
In this research, the expression of NEAT1 and miR-1224-5p in gastric cancer tissues was measured by qRT-PCR analysis, and the expression of remodeling and spacing factor 1 (RSF1) was measured by IHC assay. Then, the bioinformatics prediction software ENCORI was applied to envisage the assumed binding sites. The monitoring roles of NEAT1 or miR-1224-5p on the cell proliferation and migration capacity were verified by CCK-8, wound healing and transwell assay, correspondingly. The interactions among NEAT1, miR-1224-5p and RSF1 were investigated via luciferase analysis.
Results:
Our findings revealed high expression levels of NEAT1, RSF1 and a decreased expression level of miR-1224-5p in gastric cancer. Upregulation of NEAT1 or knockdown of miR-1224-5p elevated gastric cancer cell proliferation, and migration. Bioinformatics and luciferase analyses simplified that NEAT1 directly cooperated with miR-1224-5p to weaken miR-1224-5p binding to the RSF1 3'-UTR region. Likewise, the mechanical inquiries ratified that initiation of the miR-1224-5p/RSF1 regulatory loop by miR-1224-5p knockdown or overexpressed RSF1 validated the functions of NEAT1 in endorsing gastric cancer cell malignancy.
Discussion:
Our research initially validated that NEAT1 may regulate the expression of RSF1 competitive sponge to miR-1224-5p, contributed to the supervision of gastric cancer evolution, which exposed new brightness for diagnosis and therapy of gastric cancer.
Insights
Nuclear paraspeckle assembly transcript 1 (NEAT1) promotes gastric cancer progression by sponging miR-1224-5p, leading to increased remodeling and spacing factor 1 (RSF1) expression. This finding offers new avenues for gastric cancer diagnosis and therapy.
Area of Science:
- Molecular Oncology
- Epigenetics
- Cancer Biology
Background:
- Advanced gastric cancer presents significant therapeutic challenges.
- Long non-coding RNAs (lncRNAs) are implicated in gastric cancer, but specific roles like NEAT1 remain underexplored.
Purpose of the Study:
- To investigate the functional role and molecular mechanism of NEAT1 in gastric cancer.
- To elucidate the regulatory relationship between NEAT1, miR-1224-5p, and RSF1 in gastric cancer progression.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and immunohistochemistry (IHC) to assess NEAT1, miR-1224-5p, and RSF1 expression.
- Bioinformatics analysis (ENCORI) for predicting binding sites.
- Cell proliferation (CCK-8), migration (wound healing, Transwell), and interaction (luciferase) assays to validate molecular mechanisms.
Main Results:
- NEAT1 and RSF1 were highly expressed, while miR-1224-5p was decreased in gastric cancer tissues.
- NEAT1 upregulation enhanced gastric cancer cell proliferation and migration.
- NEAT1 acts as a molecular sponge for miR-1224-5p, inhibiting its binding to RSF1 and promoting cancer cell malignancy.
Conclusions:
- NEAT1 regulates RSF1 expression via competitive sponging of miR-1224-5p.
- This regulatory axis contributes to gastric cancer progression.
- Findings provide novel insights for gastric cancer diagnosis and therapeutic strategies.
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