1. Academic Validation
  2. Ginsenoside Rh2 enhances the antitumor immunological response of a melanoma mice model

Ginsenoside Rh2 enhances the antitumor immunological response of a melanoma mice model

  • Oncol Lett. 2017 Feb;13(2):681-685. doi: 10.3892/ol.2016.5490.
Meng Wang 1 Shi-Ju Yan 2 Hong-Tao Zhang 2 Nan Li 2 Tao Liu 2 Ying-Long Zhang 2 Xiao-Xiang Li 2 Qiong Ma 2 Xiu-Chun Qiu 2 Qing-Yu Fan 2 Bao-An Ma 2
Affiliations

Affiliations

  • 1 Department of Orthopedic Surgery Center and Orthopedic Oncology Institute of People's Liberation Army, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, P.R. China; Department of Spine and Joint Surgery, Center of the Chinese People's Liberation Army Lanzhou Military Region, The 11th Hospital of the People's Liberation Army, Xinjiang 835000, P.R. China.
  • 2 Department of Orthopedic Surgery Center and Orthopedic Oncology Institute of People's Liberation Army, Tangdu Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, P.R. China.
Abstract

The treatment of malignant tumors following surgery is important in preventing relapse. Among all the post-surgery treatments, immunomodulators have demonstrated satisfactory effects on preventing recurrence according to recent studies. Ginsenoside is a compound isolated from panax ginseng, which is a famous traditional Chinese medicine. Ginsenoside aids in killing tumor cells through numerous processes, including the antitumor processes of ginsenoside Rh2 and Rg1, and also affects the inflammatory processes of the immune system. However, the role that ginsenoside serves in antitumor immunological activity remains to be elucidated. Therefore, the present study aimed to analyze the effect of ginsenoside Rh2 on the antitumor immunological response. With a melanoma mice model, ginsenoside Rh2 was demonstrated to inhibit tumor growth and improved the survival time of the mice. Ginsenoside Rh2 enhanced T-lymphocyte infiltration in the tumor and triggered cytotoxicity in spleen lymphocytes. In addition, the immunological response triggered by ginsenoside Rh2 could be transferred to other mice. In conclusion, the present study provides evidence that ginsenoside Rh2 treatment enhanced the antitumor immunological response, which may be a potential therapy for melanoma.

Keywords

animals; cytotoxic T lymphocytes; ginsenoside Rh2 (GRh2); immunotherapy; melanoma; mice; tumor.

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