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Updated: Mar 1, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-338-3p inhibits thyroid cancer progression through targeting AKT3
Guo-Qing Sui1, Dan Fei1, Feng Guo1
1Department of Ultrasound, The China-Japan Union Hospital of Jilin UniversityChangchun 130033, China.
Abstract:
microRNA-338-3p (miR-338-3p) has been implicated in tumor development and progression in many types of cancers. However, the function and mechanism underlying the action of miR-383-3p in thyroid cancer remain unclear and were therefore investigated in this study by in vitro and in vivo experiments. We found that miR-338-3p was downregulated in thyroid cancer tissues and cell lines. miR-338-3p expression was significantly associated with the clinical stage and lymph node metastasis of thyroid cancer. Forced expression of miR-338-3p suppressed thyroid cancer cell proliferation, clonogenicity, migration, and invasion in vitro and inhibited tumorigenesis in a nude mouse xenograft model system. Moreover, AKT3, a known oncogene, was confirmed as a direct target of miR-383-3p in thyroid cancer cells, as evidenced by the fact that ectopic miR-383 expression suppressed AKT3 expression and its downstream pathway (AKT pathway). In addition, AKT3 silencing by siRNA mimicked the effect of ectopic miR-338-3p on the growth and invasion of thyroid cancer cells. In contrast, AKT3 overexpression attenuated the inhibitory effect induced by miR-338-3p overexpression in thyroid cancer cells. These results suggest that miR-338-3p functions as a novel tumor suppressor that blocks thyroid cancer cell growth through targeting AKT3.
Insights
microRNA-338-3p (miR-338-3p) acts as a tumor suppressor in thyroid cancer. Its downregulation promotes cancer progression, while restoring miR-338-3p inhibits growth by targeting the oncogene AKT3.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- microRNA-338-3p (miR-338-3p) is linked to various cancers.
- Its specific role in thyroid cancer pathogenesis is not well understood.
Purpose of the Study:
- To investigate the function and mechanism of miR-338-3p in thyroid cancer.
- To determine if miR-338-3p acts as a tumor suppressor.
Main Methods:
- In vitro and in vivo experiments were conducted.
- Thyroid cancer tissues and cell lines were analyzed for miR-338-3p expression.
- Target validation was performed using techniques like Western blotting and siRNA.
- Nude mouse xenograft models were used for tumorigenesis studies.
Main Results:
- miR-338-3p was found to be downregulated in thyroid cancer tissues and cell lines.
- Lower miR-338-3p expression correlated with advanced clinical stage and lymph node metastasis.
- Overexpression of miR-338-3p inhibited thyroid cancer cell proliferation, migration, invasion, and in vivo tumor growth.
- AKT3 was identified as a direct target of miR-338-3p, and its suppression mediated the anti-cancer effects.
Conclusions:
- miR-338-3p functions as a tumor suppressor in thyroid cancer.
- It inhibits cancer cell growth and invasion by targeting the oncogene AKT3.
- Restoring miR-338-3p levels may offer a therapeutic strategy for thyroid cancer.
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