Lycorine hydrochloride inhibits melanoma cell proliferation, migration and invasion via down-regulating p21Cip1/WAF1

Lycorine hydrochloride (LH) is an active ingredient sourced from the medicinal herb Lycoris radiata. Previous studies have suggested that LH exerts tumor suppression activity in several human cancers. However, the anti-cancer effect of LH in melanoma and the potential molecular mechanisms still need to be further studied. p21(Cip1/WAF1), unlike its traditional cyclin-dependent kinase (CDK) inhibitor role, is believed to act as an oncogene under certain cellular conditions. In this research, an increased expression of p21(Cip1/WAF1) was found in human melanoma tissues and positively related to the tumor invasion depth. High level of p21(Cip1/WAF1) was found to correlate with bad outcomes of melanoma patients by Kaplan-Meier survival analysis. Functional experiments demonstrated that the proliferation, migration and invasion ability of A375 and MV3 melanoma cells was powerfully inhibited by LH through inducing S phase cell cycle arrest and regulating epithelial-mesenchymal transition (EMT). In NOD/SCID mice model, LH effectively inhibited the xenograft tumor growth and lung metastasis of A375 cells. Further research revealed that LH reduced p21(Cip1/WAF1) protein by accelerating its ubiquitination. Importantly, the LH-induced suppression of cell proliferation and metastasis was rescued by p21(Cip1/WAF1) overexpression, both in vitro an in vivo. Taken together, LH, which suppresses the proliferation and metastasis of melanoma cells via down-regulating p21(Cip1/WAF1), is expected to be developed as an effective medicine for melanoma therapy.

Automated summary

The active ingredient Lycorine hydrochloride sourced from the medicinal herb Lycoris radiata has been shown to possess tumor suppression activity in various human cancers. In melanoma, an increased expression of p21(Cip1/WAF1) was found in tumor tissues and correlated with tumor invasion depth. Functional experiments demonstrated that LH effectively inhibited the proliferation, migration, and invasion ability of melanoma cells by inducing S phase cell cycle arrest and regulating epithelial-mesenchymal transition (EMT).