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Updated: Mar 8, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Tumor suppressor miR-1 inhibits tumor growth and metastasis by simultaneously targeting multiple genes
Cuilian Liu1, Song Zhang1, Qizhi Wang2
1College of Life Sciences and Laboratory for Marine Biology and Biotechnology of Qingdao National Laboratory for Marine Science and Technology, Zhejiang University, Hangzhou 310058, The People's Republic of China.
Abstract:
Cancer progression depends on tumor growth and metastasis, which are activated or suppressed by multiple genes. An individual microRNA may target multiple genes, suggesting that a miRNA may suppress tumor growth and metastasis via simultaneously targeting different genes. However, thus far, this issue has not been explored. In the present study, the findings showed that miR-1 could simultaneously inhibit tumor growth and metastasis of gastric and breast cancers by targeting multiple genes. The results indicated that miR-1 was significantly downregulated in cancer tissues compared with normal tissues. The miR-1 overexpression led to cell cycle arrest in the G1 phase in gastric and breast cancer cells but not in normal cells. Furthermore, the miR-1 overexpression significantly inhibited the metastasis of gastric and breast cancer cells. An analysis of the underlying mechanism revealed that the simultaneous inhibition of tumor growth and metastasis mediated by miR-1 was due to the synchronous targeting of 6 miR-1 target genes encoding cyclin dependent kinase 4, twinfilin actin binding protein 1, calponin 3, coronin 1C, WAS protein family member 2 and thymosin beta 4, X-linked. In vivo assays demonstrated that miR-1 efficiently inhibited tumor growth and metastasis of gastric and breast cancers in nude mice. Therefore, our study contributed novel insights into the miR-1's roles in tumorigenesis of gastric and breast cancers.
Insights
MicroRNA-1 (miR-1) suppresses gastric and breast cancer growth and metastasis by targeting multiple genes. This study reveals miR-1
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Cancer progression involves complex gene regulation of tumor growth and metastasis.
- MicroRNAs (miRNAs) are known to regulate multiple genes, suggesting potential for simultaneous control of cancer processes.
- The specific role of individual miRNAs in concurrently inhibiting both tumor growth and metastasis has not been extensively studied.
Purpose of the Study:
- To investigate the role of miR-1 in simultaneously inhibiting tumor growth and metastasis in gastric and breast cancers.
- To identify the molecular mechanisms by which miR-1 exerts its tumor-suppressive effects.
- To explore the therapeutic potential of miR-1 in gastric and breast cancer treatment.
Main Methods:
- Analysis of miR-1 expression levels in cancer versus normal tissues.
- In vitro experiments involving miR-1 overexpression in gastric and breast cancer cell lines to assess cell cycle and metastatic potential.
- Bioinformatic analysis and experimental validation to identify miR-1 target genes.
- In vivo studies using nude mouse models to evaluate the effect of miR-1 on tumor growth and metastasis.
Main Results:
- miR-1 was significantly downregulated in gastric and breast cancer tissues.
- Overexpression of miR-1 induced G1 phase cell cycle arrest in cancer cells and suppressed their metastatic capabilities.
- miR-1 was found to simultaneously target six genes involved in cell cycle regulation and cell motility.
- In vivo assays confirmed that miR-1 inhibits tumor growth and metastasis in gastric and breast cancer models.
Conclusions:
- miR-1 acts as a tumor suppressor in gastric and breast cancers by simultaneously inhibiting tumor growth and metastasis.
- The mechanism involves the coordinated targeting of multiple genes regulating cell cycle and cell motility.
- miR-1 represents a promising therapeutic target for gastric and breast cancer treatment.
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