Abstract

Ginsenoside Ro (Ro), a major saponin derived and isolated from Panax ginseng C.A. Meyer, exerts multiple biological activities. However, the anti-tumour efficacy of Ro remains unclear because of its poor in vitro effects. In this study, we confirmed that Ro has no anti-tumour activity in vitro. We explored the anti-tumour activity of Ro in vivo in B16F10 tumour-bearing mice. The results revealed that Ro considerably suppressed tumour growth with no significant side effects on immune organs and body weight. Zingibroside R1, chikusetsusaponin IVa, and calenduloside E, three metabolites of Ro, were detected in the plasma of Ro-treated tumour-bearing mice and showed excellent anti-tumour effects as well as anti-angiogenic activity. The results suggest that the metabolites play important roles in the anti-tumour efficacy of Ro in vivo. Additionally, the haemolysis test demonstrated that Ro has good biocompatibility. Taken together, the findings of this study demonstrate that Ro markedly suppresses the tumour growth of B16F10-transplanted tumours in vivo, and its anti-tumour effects are based on the biological activity of its metabolites. The anti-tumour efficacy of these metabolites is due, at least in part, to its anti-angiogenic activity.

Highlights

  • Skin cancer is a common type of cancer with an increasing incidence rate and public health burden [1]

  • The results showed that Ro has anti-tumour activity, and its efficacy is through its metabolites

  • The anti-tumour effects of Ro were evaluated in a xenograft mouse model

Read more

Summary

Introduction

Skin cancer is a common type of cancer with an increasing incidence rate and public health burden [1]. As the most aggressive form of skin cancer, melanoma is a devastating disease as it is highly metastatic and has a poor prognosis once metastasis has occurred; there is no therapy that has consistently improved overall survival in patients with metastatic melanoma [2,3]. Melanoma originates from melanocytes, specialised pigmented cells found in the epidermis [4]. Patients with this disease have an increased risk of developing subsequent primary melanoma [5]. Its incidence has increased faster than that of any other cancer type during recent decades.

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call