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Updated: Mar 28, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-663 suppresses cell invasion and migration by targeting transforming growth factor beta 1 in papillary
Zhihong Wang1, Hao Zhang2, Ping Zhang1
1Department of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, 110001, People's Republic of China.
Abstract:
MicroRNA-663 (miR-663) has been detected in a large variety of tumor types; however, it still holds both tumor suppressive and oncogenic roles in different tumor types. The miRNA-CHIP microarray assay revealed downregulation of miR-663 in papillary thyroid carcinoma (PTC); however, the effect of miR-663 on PTC cell invasion and migration remains unknown. Accordingly, this study aimed to investigate the potential involvement of miR-663 in PTC. In this study, miR-663 expression level was measured via quantitative real-time PCR in 91 pairs of human PTC and adjacent normal tissues and in two human PTC cell lines. The effect of miR-663 on PTC cell invasion and migration were studied by transwell and wound healing assays. In addition, the miR-663 target was searched and the underlying mechanism was clarified by reporter assay and rescue experiment. The current study confirmed that miR-663 expression was inhibited in PTC tissue samples and PTC cell lines. There were statistically significant differences in expression of miR-663 with regard to age and tumor size. Upregulation of miR-663 suppressed PTC cell invasion and migration. Further study showed that transforming growth factor beta 1 (TGFβ1) was the direct target of miR-663 and mediated the effect of miR-663 on PTC development. By targeting TGFβ1, miR-663 efficiently regulates the expression of epithelial-mesenchymal transition (EMT) markers and matrix metalloproteinases (MMPs). The data indicated that miR-663 may suppress tumor invasion and migration by targeting TGFβ1 and regulate EMT progress of PTC cells.
Insights
MicroRNA-663 (miR-663) is downregulated in papillary thyroid carcinoma (PTC). Upregulating miR-663 suppresses PTC cell invasion and migration by targeting transforming growth factor beta 1 (TGFβ1).
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- MicroRNA-663 (miR-663) exhibits dual roles in various cancers.
- Downregulation of miR-663 was observed in papillary thyroid carcinoma (PTC) via microarray analysis.
- The specific function of miR-663 in PTC cell invasion and migration remained unclear.
Purpose of the Study:
- To investigate the role of miR-663 in papillary thyroid carcinoma (PTC).
- To determine the effect of miR-663 on PTC cell invasion and migration.
- To elucidate the underlying molecular mechanism of miR-663 in PTC.
Main Methods:
- Quantitative real-time PCR to measure miR-663 expression in 91 PTC tissues and cell lines.
- Transwell and wound healing assays to assess PTC cell invasion and migration.
- Reporter assays and rescue experiments to identify miR-663 targets and mechanisms.
Main Results:
- miR-663 expression was significantly inhibited in PTC tissues and cell lines.
- miR-663 upregulation suppressed PTC cell invasion and migration.
- Transforming growth factor beta 1 (TGFβ1) was identified as a direct target of miR-663.
- miR-663 regulates epithelial-mesenchymal transition (EMT) markers and matrix metalloproteinases (MMPs) via TGFβ1.
Conclusions:
- miR-663 acts as a tumor suppressor in PTC.
- miR-663 inhibits PTC cell invasion and migration by targeting TGFβ1.
- Targeting TGFβ1 by miR-663 regulates EMT progression in PTC.
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