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ALPHA.-Solanine Inhibits Human Melanoma Cell Migration and Invasion by Reducing Matrix Metalloproteinase-2/9 Activities

Authors :
Tzu-Tsung Chang Chien
Li-Heng Fang
Yuan-Wei Shih
Ming-Kun Lu
Pin-Shern Chen
Hsiang-Ching Huang
Source :
Biological and Pharmaceutical Bulletin. 33:1685-1691
Publication Year :
2010
Publisher :
Pharmaceutical Society of Japan, 2010.

Abstract

α-Solanine, a naturally occurring steroidal glycoalkaloid in potato sprouts, was found to possess anti-carcinogenic properties, such as inhibiting proliferation and inducing apoptosis of tumor cells. However, the effect of α-solanine on cancer metastasis remains unclear. In the present study, we examined the effect of α-solanine on metastasis in vitro. Data demonstrated that α-solanine inhibited proliferation of human melanoma cell line A2058 in a dose-dependent manner. When treated with non-toxic doses of α-solanine, cell migration and invasion were markedly suppressed. Furthermore, α-solanine reduced the activity of matrix metalloproteinase-2 (MMP-2) and MMP-9, which are involved in the migration and invasion of cancer cells. Our biochemical assays indicated that α-solanine potently suppressed the phosphorylation of c-Jun N-terminal kinase (JNK), phosphatidylinositide-3 kinase (PI3K) and Akt, while it did not affect phosphorylation of extracellular signal regulating kinase (ERK). In addition, α-solanine significantly decreased the nuclear level of nuclear factor kappa B (NF-κB), suggesting that α-solanine inhibited NF-κB activity. Taken together, the results suggested that α-solanine inhibited migration and invasion of A2058 cells by reducing MMP-2/9 activities. It also inhibited JNK and PI3K/Akt signaling pathways as well as NF-κB activity. These findings reveal new therapeutic potential for α-solanine in anti-metastatic therapy.

Details

ISSN :
13475215 and 09186158
Volume :
33
Database :
OpenAIRE
Journal :
Biological and Pharmaceutical Bulletin
Accession number :
edsair.doi.dedup.....f3cea2f2fdd5e969a541b4219422e104
Full Text :
https://doi.org/10.1248/bpb.33.1685