Publication: 13-Butoxyberberine Bromide Inhibits Migration and Invasion in Skin Cancer A431 Cells
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Issued Date
2023
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File Type
application/pdf
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มหาวิทยาลัยศรีนครินทรวิโรฒ
Bibliographic Citation
Molecules. Vol 28, No.3 (2023)
Suggested Citation
Laomethakorn P., Tayeh M., Samosorn S., Tananyuthawongse C., Watanapokasin R. 13-Butoxyberberine Bromide Inhibits Migration and Invasion in Skin Cancer A431 Cells. Molecules. Vol 28, No.3 (2023). doi:10.3390/molecules28030991 Retrieved from: https://hdl.handle.net/20.500.14740/12544
Other Contributor(s)
Abstract
Cancer metastasis is the primary cause of cancer morbidity and mortality. Anti-metastasis mechanism of skin cancer by 13-butoxyberberine bromide, a novel berberine derivative, has not yet been reported. This study investigated the effects of 13-butoxyberberine bromide on migration and invasion of skin cancer A431 cells. The cytotoxicity of 13-butoxyberberine bromide was determined by MTT assay. The effect of 13-butoxyberberine bromide on cell migration and invasion were examined using a wound-healing assay, transwell migration assay, and transwell invasion assay, respectively. The cell adhesion ability was determined by an adhesion assay. Protein expressions that play important roles in cancer migration and invasion were evaluated by Western blot analysis. The results showed that 13-butoxyberberine bromide effectively inhibited cell migration, invasion, and adhesion in A431 cells. Interestingly, 13-butoxyberberine bromide was more effective for cell migration inhibition than berberine. In addition, 13-butoxyberberine bromide showed anti-migration and anti-invasion effects by down-regulated MMP-2 and MMP-9 expression and up-regulated TIMP-1 and TIMP-2 expression in A431 cells. Moreover, pretreatment with 13-butoxyberberine bromide significantly inhibited EGF-induced cell migration and p-EGFR, ERK, p-ERK, STAT3, and p-STAT3 expressions in A431 cells at lower concentrations when compared with the berberine. These findings indicated that 13-butoxyberberine bromide could be further developed as an anticancer agent. © 2023 by the authors.