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Updated: Oct 6, 2025

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
LncRNA NR2F2-AS1 functions as a tumor suppressor in gastric cancer through targeting miR-320b/PDCD4 pathway
Ming Luo1, Shuangya Deng1, Tong Han1
1Department of General Surgery, The Second Xiangya Hospital, Central South University, Changsha, PR China.
Abstract:
Gastric cancer is among the most frequently occurring gastrointestinal malignancies with a high mortality rate worldwide. Long non-coding RNAs (lncRNAs) are defined as core regulators in the occurrence and progression of multiple cancers, including gastric carcinoma. Mounting evidence has indicated that NR2F2-AS1 can inhibit several malignant tumors. However, the function and potential mechanism of NR2F2-AS1 remain unclear. In the current study, we found that NR2F2-AS1 was weakly expressed in gastric cancer cells in comparison with normal cells. The study has further disclosed that ectopic of NR2F2-AS1 repressed cell proliferation, migration, invasion and EMT whereas it promoted cell apoptosis in gastric carcinoma. Subsequently, our results confirmed that miR-320b was negatively regulated and that suppression of miR-320b alleviated the malignant behaviors of GC cells. More importantly, PDCD4 was a target of miR-320b. Mechanistically, NR2F2-AS1 modulated the expression level of PDCD4 by sponging miR-320b. Finally, rescue assays demonstrated that NR2F2-AS1 down-regulated PDCD4 expression to restrain the development of gastric cancer by competitively binding to miR-320b. On the whole, our study revealed the role of NR2F2-AS1/miR-320b/PDCD4 regulatory network in gastric cancer, suggesting NR2F2-AS1 may represent a novel therapeutic target for patients with gastric carcinoma.
Insights
The long non-coding RNA NR2F2-AS1 inhibits gastric cancer progression by downregulating PDCD4 expression through the miR-320b pathway. This finding suggests NR2F2-AS1 as a potential therapeutic target for gastric carcinoma.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer is a leading cause of cancer mortality globally.
- Long non-coding RNAs (lncRNAs) play crucial roles in cancer development.
- NR2F2-AS1 is implicated in inhibiting various malignant tumors, but its role in gastric cancer is unclear.
Purpose of the Study:
- To investigate the function and mechanism of NR2F2-AS1 in gastric cancer.
- To elucidate the regulatory network involving NR2F2-AS1, miR-320b, and PDCD4 in gastric carcinoma.
Main Methods:
- Quantitative real-time PCR to assess NR2F2-AS1 expression.
- Cell proliferation, migration, invasion, and apoptosis assays.
- Western blotting to detect protein expression.
- MiR-320b mimic and inhibitor transfection.
- Luciferase reporter assays to confirm target interactions.
Main Results:
- NR2F2-AS1 expression was significantly downregulated in gastric cancer tissues and cells.
- Overexpression of NR2F2-AS1 suppressed gastric cancer cell proliferation, migration, invasion, and epithelial-mesenchymal transition (EMT), while promoting apoptosis.
- NR2F2-AS1 acted as a molecular sponge for miR-320b, inhibiting its activity.
- PDCD4 was identified as a direct target of miR-320b.
- NR2F2-AS1 exerted its tumor-suppressive effects by downregulating PDCD4 via sponging miR-320b.
Conclusions:
- NR2F2-AS1 functions as a tumor suppressor in gastric cancer.
- The NR2F2-AS1/miR-320b/PDCD4 axis plays a critical role in regulating gastric cancer progression.
- NR2F2-AS1 holds potential as a novel therapeutic target for gastric cancer treatment.
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