4.0 Article

Pitavastatin Induces Apoptosis of Cutaneous Squamous Cell Carcinoma Cells through Geranylgeranyl Pyrophosphate-Dependent c-Jun N-Terminal Kinase Activation

Journal

ANNALS OF DERMATOLOGY
Volume 35, Issue 2, Pages 116-123

Publisher

KOREAN DERMATOLOGICAL ASSOC
DOI: 10.5021/ad.22.139

Keywords

Apoptosis; c -Jun N -terminal kinase; Pitavastatin; Squamous cell carcinoma cells

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This study investigates the action mechanisms of the cholesterol-lowering drug pitavastatin on cutaneous squamous cell carcinoma (SCC) cells. The results show that pitavastatin dose-dependently induces apoptosis of cutaneous SCC cells, but has no effect on normal keratinocytes. Further experiments reveal that pitavastatin-induced apoptosis is achieved through GGPP-dependent JNK activation.
Background: Pitavastatin is a cholesterol-lowering drug and is widely used clinically. In ad-dition to this effect, pitavastatin has shown the potential to induce apoptosis in cutaneous squamous cell carcinoma (SCC) cells.Objective: The purpose of this study is to investigate the effects and possible action mecha-nisms of pitavastatin.Methods: SCC cells (SCC12 and SCC13 cells) were treated with pitavastatin, and induc-tion of apoptosis was confirmed by Western blot. To examine whether pitavastatin-induced apoptosis is related to a decrease in the amount of intermediate mediators in the cholesterol synthesis pathway, the changes in pitavastatin-induced apoptosis after supplementation with mevalonate, squalene, geranylgeranyl pyrophosphate (GGPP) and dolichol were investigated.Results: Pitavastatin dose-dependently induced apoptosis of cutaneous SCC cells, but the viability of normal keratinocytes was not affected by pitavastatin at the same concentra-tions. In supplementation experiments, pitavastatin-induced apoptosis was inhibited by the addition of mevalonate or downstream metabolite GGPP. As a result of examining the effect on intracellular signaling, pitavastatin decreased Yes1 associated transcriptional regulator and Ras homolog family member A and increased Rac family small GTPase 1 and c-Jun N -terminal kinase (JNK) activity. All these effects of pitavastatin on signaling molecules were restored when supplemented with either mevalonate or GGPP. Furthermore, pitavastatin-induced apoptosis of cutaneous SCC cells was inhibited by a JNK inhibitor.Conclusion: These results suggest that pitavastatin induces apoptosis of cutaneous SCC cells through GGPP-dependent JNK activation.

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