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Updated: Dec 5, 2025

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Published on: April 6, 2012
Long noncoding RNA FGF14-AS2 inhibits breast cancer metastasis by regulating the miR-370-3p/FGF14 axis
Yucui Jin1,2, Ming Zhang2, Rui Duan2
1Jiangsu Key Laboratory of Xenotransplantation, Nanjing Medical University, Longmian Road 101, Nanjing, People's Republic of China.
Abstract:
Long noncoding RNAs (lncRNAs) have emerged as important regulators in cancers, including breast cancer. However, the overall biological roles and clinical significance of most lncRNAs are not fully understood. This study aimed to elucidate the potential role of a novel lncRNA FGF14-AS2 and the mechanisms underlying metastasis in breast cancer. The lncRNA FGF14-AS2 was significantly downregulated in breast cancer tissues; patients with lower FGF14-AS2 expression had advanced clinical stage. In vitro and in vivo assays of FGF14-AS2 alterations revealed a complex integrated phenotype affecting breast cancer cell migration, invasion, and tumor metastasis. Mechanistically, FGF14-AS2 functioned as a competing endogenous RNA of miR-370-3p, thereby leading to the activation of its coding counterpart, FGF14. Clinically, we observed increased miR-370-3p expression in breast cancer tissues, whereas FGF14 expression was decreased in breast cancer tissues compared to the adjacent normal breast tissues. FGF14-AS2 expression was significantly negatively correlated with miR-370-3p expression, and correlated positively to FGF14 expression. Collectively, our findings support a model in which the FGF14-AS2/miR-370-3p/FGF14 axis is a critical regulator in breast cancer metastasis, suggesting a new therapeutic direction in breast cancer.
Insights
The long noncoding RNA FGF14-AS2 is downregulated in breast cancer, suppressing metastasis by regulating the miR-370-3p/FGF14 axis. Lower FGF14-AS2 indicates advanced disease, suggesting therapeutic potential.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are key regulators in cancer, but their roles in breast cancer metastasis remain incompletely understood.
- Identifying novel lncRNAs and their mechanisms is crucial for understanding breast cancer progression and developing targeted therapies.
Purpose of the Study:
- To investigate the role of the novel lncRNA FGF14-AS2 in breast cancer metastasis.
- To elucidate the underlying molecular mechanisms involving FGF14-AS2 in breast cancer progression.
Main Methods:
- Analysis of FGF14-AS2 expression in breast cancer tissues and correlation with clinical stage.
- In vitro and in vivo experiments to assess the functional impact of FGF14-AS2 alterations on cancer cell behavior.
- Mechanistic studies to identify interactions between FGF14-AS2, miR-370-3p, and FGF14.
Main Results:
- FGF14-AS2 was significantly downregulated in breast cancer tissues, with lower expression linked to advanced clinical stage.
- Altered FGF14-AS2 levels affected breast cancer cell migration, invasion, and tumor metastasis in vitro and in vivo.
- FGF14-AS2 acts as a competing endogenous RNA for miR-370-3p, leading to FGF14 activation.
- miR-370-3p was upregulated, and FGF14 was downregulated in breast cancer tissues.
- FGF14-AS2 expression inversely correlated with miR-370-3p and positively with FGF14.
Conclusions:
- The FGF14-AS2/miR-370-3p/FGF14 axis is a critical regulator of breast cancer metastasis.
- FGF14-AS2 functions as a tumor suppressor by inhibiting metastasis through this axis.
- This axis represents a potential therapeutic target for breast cancer treatment.
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