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Updated: Mar 31, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
miR-29a suppresses growth and metastasis in papillary thyroid carcinoma by targeting AKT3
1Institute of Virology and AIDS Research, The First Hospital of Jilin University, Changchun, 130021, China.
Abstract:
MicroRNA-29a (miR-29a) has been reported to play important roles in tumor initiation, development, and metastasis in various cancers. However, the biological function and potential mechanisms of miR-29a in papillary thyroid carcinoma (PTC) remain unclear. In the present study, we discovered that miR-29a was frequently downregulated in PTC tissues, and its expression was significantly associated with tumor size, TNM stage, and lymph node metastasis. Functional assays showed that overexpression of miR-29a markedly suppressed PTC cell proliferation, migration, and invasion and promoted PTC apoptosis and cell cycle arrest at G0/G1 phase. In vivo, miR-29a overexpression decreased tumor growth in a xenograft mouse model. Luciferase reporter assay showed that miR-29a can directly bind to the 3' untranslated region (UTR) of AKT3 in PTC cells. Overexpreesion of miR‑29a obviously decreased AKT3 expression, thereby suppressing phosphatidylinositol 3-kinase (PI3K)/AKT pathway activation. We also confirmed that AKT3 expression was increased in PTC tissue and was inversely correlated miR-29a expression in PTC tissues. In addition, downregulation of AKT3 by siRNA mimicked the effects of miR-29a overexpression, and upregulation of AKT3 partially reversed the inhibitory effects of miR-29a. These results suggested that miR-29a could act as a tumor suppressor in PTC by targeting AKT3 and that miR-29a may potentially serve as an anti-tumor agent in the treatment of PTC.
Insights
MicroRNA-29a (miR-29a) acts as a tumor suppressor in papillary thyroid carcinoma (PTC). Downregulation of miR-29a promotes PTC growth and metastasis by targeting AKT3, suggesting its potential as an anti-tumor agent.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-29a (miR-29a) is implicated in various cancers, but its role in papillary thyroid carcinoma (PTC) is not well understood.
- Understanding miR-29a's function in PTC is crucial for developing new therapeutic strategies.
Purpose of the Study:
- To investigate the biological function and molecular mechanisms of miR-29a in papillary thyroid carcinoma.
- To determine if miR-29a can serve as a potential therapeutic target for PTC.
Main Methods:
- Analysis of miR-29a expression in PTC tissues and correlation with clinicopathological features.
- In vitro functional assays (cell proliferation, migration, invasion, apoptosis, cell cycle) and in vivo xenograft mouse models.
- Luciferase reporter assays to identify miR-29a targets, including AKT3, and investigation of the PI3K/AKT pathway.
Main Results:
- miR-29a was significantly downregulated in PTC tissues and associated with tumor size, TNM stage, and lymph node metastasis.
- Overexpression of miR-29a suppressed PTC cell proliferation, migration, and invasion, induced apoptosis, and caused cell cycle arrest.
- miR-29a directly targets AKT3, inhibiting the PI3K/AKT pathway; AKT3 was upregulated in PTC and inversely correlated with miR-29a levels.
Conclusions:
- miR-29a functions as a tumor suppressor in PTC by targeting AKT3 and inhibiting the PI3K/AKT pathway.
- Restoration of miR-29a expression may represent a novel therapeutic approach for papillary thyroid carcinoma treatment.
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