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Updated: Oct 7, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-603 Promotes Progression of Cutaneous Melanoma by Regulating TBX5
Xianghua Dong1, Ying Wang2, Yan Qu3
1Department of Dermatology, Yantai Municipal Laiyang Central Hospital, 265200, China.
Background:
Although studies manifested that microRNA-603 plays a vital role in many cancers, the modulatory mechanism of microRNA-603 in cutaneous melanoma remains unknown. We aimed to investigate the roles of microRNA-603 in cutaneous melanoma cells.
Methods:
First, microRNA-603 expression in cutaneous melanoma cell lines was detected by qRT-PCR. The mRNA and protein expression levels of TBX5 in cutaneous melanoma cell lines were tested by qRT-PCR and western blot, respectively. In addition, the interaction between microRNA-603 and TBX5 was determined by dual-luciferase reporter gene assay, and their impacts on the growth of cutaneous melanoma cells were detected by cellular function experiments such as MTT, colony formation, and Transwell assays.
Results:
The expression level of microRNA-603 in human cutaneous melanoma cells was relatively upregulated. Overexpressing microRNA-603 could promote progression of cutaneous melanoma cells, while silencing microRNA-603 expression could suppress the malignant progression of cutaneous melanoma. In addition, TBX5 was lowly expressed in cutaneous melanoma cells. As confirmed by dual-luciferase assay, microRNA-603 could specifically bind to 3'UTR of TBX5 and regulate TBX5. The results of the rescue experiment demonstrated that inhibiting microRNA-603 expression could suppress the proliferation, migration, and invasion of cutaneous melanoma cells, but its suppressive effect could be restored by TBX5.
Conclusion:
MicroRNA-603 could regulate the expression of TBX5, thus promoting the malignant progression of cutaneous melanoma cells.
Insights
MicroRNA-603 promotes cutaneous melanoma progression by regulating TBX5. Silencing microRNA-603 suppressed tumor growth, while TBX5 partially restored it, revealing a novel regulatory mechanism in skin cancer.
Area of Science:
- Oncology
- Molecular Biology
- Dermatology
Background:
- MicroRNA-603 is implicated in various cancers, but its role in cutaneous melanoma is unclear.
- Understanding microRNA-603's mechanism in skin cancer is crucial for targeted therapies.
Purpose of the Study:
- To investigate the role and mechanism of microRNA-603 in cutaneous melanoma.
- To determine the relationship between microRNA-603 and TBX5 in melanoma cells.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and Western blot to assess microRNA-603 and TBX5 expression.
- Dual-luciferase reporter assay to confirm the interaction between microRNA-603 and TBX5.
- Cellular assays (MTT, colony formation, Transwell) to evaluate the impact on melanoma cell growth, migration, and invasion.
Main Results:
- MicroRNA-603 was upregulated in cutaneous melanoma cells and promoted tumor progression.
- TBX5 expression was downregulated; microRNA-603 directly targeted and regulated TBX5.
- Inhibition of microRNA-603 suppressed melanoma cell proliferation, migration, and invasion, effects reversible by TBX5 restoration.
Conclusions:
- MicroRNA-603 promotes cutaneous melanoma malignancy by regulating TBX5 expression.
- This study elucidates a novel molecular pathway involving microRNA-603 and TBX5 in melanoma.
- Targeting the microRNA-603/TBX5 axis may offer therapeutic strategies for cutaneous melanoma.
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