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Updated: Dec 30, 2025

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
Published on: June 7, 2019
miRNA-183∼96∼182 regulates melanogenesis, cell proliferation and migration in B16 cells
Bin Du1, Xuexian Liu1, Ajab Khan1
1College of Animal Science and Veterinary Medicine, Shanxi Agricultural University, Taigu, 030801, China.
Abstract:
Melanoma is a highly invasive malignant skin tumor having high metastatic rate and poor prognosis. The biology of melanoma is controled by miRNAs. The miRNA-183 cluster, which is composed of miRNA-183∼96∼182 genes, plays an important roles in tumor development. In order to investigate the role and action of miRNA-183 cluster in B16 cells, we overexpressed and knocked down miRNA-183 cluster in B16 cells. Using bioinformatics analysis, we predicted that the key framscript factor of melangenic genes. Microphthalmia-associated transcription factor (MITF) is one of the targets of miRNA-183 cluster. The results of Luciferase activity assays confirmed that MITF was targeted by miRNA-183 cluster. Overexpression and knockdown of miRNA-183 cluster in B16 cells resulted in down and up regulation of MITF expression, respectively at both mRNA and protein levels. Furthmore, overexpression and knockdown of the miRNA-183 cluster in B16 cells decreased and increased the expression of mRNA and protein of melangenic genes tyrosinase (TYR), and tyrosinase-related protein 1 (TYRP1), dopachrome-tautomerase (DCT), as well as the production of melanins and eumelanin production, respectively. On the proliferation and migration pathway, overexpression and knockdown of miRNA-183 cluster increased and decreased, respectively the expression of mRNA and protein of mitogen-activated protein kinase 1 (MEK1), extracellular regulated protein kinases1/2 (ERK1/2) and cAMP-responsive-element binding protein (CREB). These results indicated that miRNA-183 cluster regulated melanogenesis in B16 cells as well as cell proliferation and migration by directly targeting MITF through migration pathway.
Insights
The miRNA-183 cluster regulates melanoma cell biology by targeting Microphthalmia-associated transcription factor (MITF). This impacts melanogenesis, cell proliferation, and migration in B16 melanoma cells.
Area of Science:
- Molecular Biology
- Cancer Research
- Genetics
Background:
- Melanoma is an aggressive skin cancer with poor prognosis.
- MicroRNAs (miRNAs) are key regulators of melanoma biology.
- The miRNA-183 cluster (miRNA-183∼96∼182) is implicated in tumor development.
Purpose of the Study:
- To investigate the role of the miRNA-183 cluster in B16 melanoma cells.
- To identify targets of the miRNA-183 cluster involved in melanoma.
- To elucidate the mechanisms by which the miRNA-183 cluster affects melanoma cell functions.
Main Methods:
- Bioinformatic analysis to predict miRNA targets.
- Overexpression and knockdown of the miRNA-183 cluster in B16 cells.
- Luciferase activity assays to confirm target interaction.
- Quantitative analysis of gene and protein expression (MITF, TYR, TYRP1, DCT, MEK1, ERK1/2, CREB).
- Assessment of melanin and eumelanin production.
Main Results:
- Microphthalmia-associated transcription factor (MITF) was identified and confirmed as a direct target of the miRNA-183 cluster.
- Modulation of the miRNA-183 cluster inversely affected MITF expression at mRNA and protein levels.
- The miRNA-183 cluster regulated the expression of melanogenesis genes (TYR, TYRP1, DCT) and melanin production.
- The miRNA-183 cluster influenced cell proliferation and migration by regulating the MEK1/ERK1/2/CREB pathway.
Conclusions:
- The miRNA-183 cluster directly targets MITF, regulating melanogenesis in B16 melanoma cells.
- The miRNA-183 cluster controls melanoma cell proliferation and migration via the MITF-mediated pathway.
- This study highlights the miRNA-183 cluster as a potential therapeutic target in melanoma.
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