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Updated: Nov 27, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
miR-152/TNS1 axis inhibits non-small cell lung cancer progression through Akt/mTOR/RhoA pathway
Jinjin Duan1, Li Wang1, Liqun Shang1
1Department of Respiratory and Critical Care Medicine, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi 710068, P.R. China.
Aim:
The purpose of the present study was to explore the function and mechanism of tensin 1 (TNS1) in non-small cell lung cancer (NSCLC) progression.
Methods:
The expression of TNS1 in NSCLC cells and tissues was assessed by RT-PCR and Western blot. Besides, Kaplan-Meier survival analysis was recruited to explore the association between TNS1 and NSCLC. Cell growth was analyzed by MTT and flow cytometry assay, while cell metastasis was determined by wound healing and transwell assays. The targeting relationship between TNS1 and miR-152 was assessed by luciferase activity assays. And Western blot was employed to determine the expression of related proteins of Akt/mTOR/RhoA pathway.
Results:
TNS1 level was boosted in NSCLC cells and tissues, related to the prognosis of NSCLC patients. Furthermore, it was proved that TNS1 promoted the growth and metastasis of NSCLC cells via Akt/mTOR/RhoA pathway. And miR-152 targeted TNS1 to affect the progression of NSCLC.
Conclusion:
miR-152/TNS1 axis inhibits the progression of NSCLC by Akt/mTOR/RhoA pathway.
Insights
Tensin 1 (TNS1) promotes non-small cell lung cancer (NSCLC) growth and metastasis. The miR-152/TNS1 axis, via the Akt/mTOR/RhoA pathway, inhibits NSCLC progression.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Non-small cell lung cancer (NSCLC) remains a leading cause of cancer mortality worldwide.
- Understanding the molecular mechanisms driving NSCLC progression is crucial for developing effective therapies.
Purpose of the Study:
- To investigate the role and mechanism of tensin 1 (TNS1) in the progression of non-small cell lung cancer (NSCLC).
- To elucidate the relationship between TNS1, miR-152, and the Akt/mTOR/RhoA signaling pathway in NSCLC.
Main Methods:
- TNS1 expression was analyzed in NSCLC cells and tissues using RT-PCR and Western blot.
- Cell proliferation, migration, and invasion were assessed using MTT, flow cytometry, wound healing, and Transwell assays.
- The interaction between TNS1 and miR-152 was confirmed via luciferase assays, and the Akt/mTOR/RhoA pathway was evaluated.
Main Results:
- TNS1 expression was significantly upregulated in NSCLC tissues and cells, correlating with poorer patient prognosis.
- TNS1 overexpression promoted NSCLC cell growth, migration, and invasion.
- TNS1 was identified as a direct target of miR-152, and the miR-152/TNS1 axis regulated NSCLC progression through the Akt/mTOR/RhoA pathway.
Conclusions:
- The miR-152/TNS1 axis plays a critical role in inhibiting NSCLC progression.
- Targeting the miR-152/TNS1 axis via the Akt/mTOR/RhoA pathway represents a potential therapeutic strategy for NSCLC.
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