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Updated: Dec 14, 2025

RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA
Published on: April 10, 2018
Long non-coding RNA PHACTR2-AS1 promotes tongue squamous cell carcinoma metastasis by regulating Snail
Fenqian Yuan1, Zhiguo Miao2, Wen Chen3
1Department of Head and Neck Surgery, Jiangxi Cancer Hospital, 519 East Beijing Road, Nanchang 330029, Jiangxi, China.
Abstract:
Long non-coding RNA is an endogenous non-coding RNA that has currently been proved to be an important player in cancer cell biology. In the present study, we investigated the biological role of PHACTR2-AS1 in tongue squamous cell carcinoma (TSCC). PHACTR2-AS1 was preferentially localized in the cytoplasm, and was notably upregulated in TSCC tissues. High PHACTR2-AS1 was correlated with tumour differentiation, metastatic clinical features, relapse and shortened survival time. Depletion of PHACTR2-AS1 did not affect TSCC cell viability and colony formation ability, whereas substantially inhibited cell migration and invasion in vitro and lung metastasis in vivo. Mechanistically, PHACTR2-AS1 could sponge miR-137 to increase Snail expression, resulting in triggering epithelial-mesenchymal transition process, thereby promoting TSCC cell metastasis. Taken together, our data for the first time elucidate the metastasis-promoting role of PHACTR2-AS1 in TSCC, hinting a new therapeutic target for metastatic TSCC patients.
Insights
Long non-coding RNA PHACTR2-AS1 promotes tongue squamous cell carcinoma metastasis by sponging miR-137 and upregulating Snail. This finding offers a potential therapeutic target for metastatic TSCC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNAs (lncRNAs) are key regulators in cancer biology.
- The role of PHACTR2-AS1 in tongue squamous cell carcinoma (TSCC) remains largely unexplored.
Purpose of the Study:
- To investigate the biological function and clinical significance of PHACTR2-AS1 in TSCC.
- To elucidate the underlying molecular mechanism of PHACTR2-AS1 in TSCC progression.
Main Methods:
- Quantitative real-time PCR to assess PHACTR2-AS1 expression in TSCC tissues and cell lines.
- Cell migration, invasion, and lung metastasis assays in vivo and in vitro.
- MiRNA-RNA immunoprecipitation and Western blot assays to explore the molecular mechanism.
Main Results:
- PHACTR2-AS1 was significantly upregulated in TSCC tissues and correlated with poor prognostic factors.
- PHACTR2-AS1 depletion inhibited TSCC cell migration, invasion, and lung metastasis.
- PHACTR2-AS1 acts as a molecular sponge for miR-137, increasing Snail expression and promoting epithelial-mesenchymal transition.
Conclusions:
- PHACTR2-AS1 plays a critical role in promoting TSCC cell metastasis.
- PHACTR2-AS1 represents a potential therapeutic target for patients with metastatic TSCC.
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