Antimetastatic Potentials ofDioscorea nipponicaon MelanomaIn VitroandIn Vivo

Author:

Ho Mao-Lin1,Hsieh Yih-Shou23,Chen Jia-Yuh1,Chen Kuo-Shuen14,Chen Jia-Jing5,Kuo Wu-Hsien67,Lin Shu-Jiuan8,Chen Pei-Ni35

Affiliation:

1. Institute of Medicine, Chung Shan Medical University, No. 110, Section 1, Jianguo N. Road, Taichung 402, Taiwan

2. Department of Biochemistry, Chung Shan Medical University, No. 110, Section 1, Jianguo N. Road, Taichung 402, Taiwan

3. Clinical Laboratory, Chung Shan Medical University Hospital, No. 110, Section 1, Jianguo N. Road, Taichung 402, Taiwan

4. Department of Internal Medicine, Chung Shan Medical University Hospital, No. 110, Section 1, Jianguo N. Road, Taichung 402, Taiwan

5. Institute of Biochemistry and Biotechnology, Chung Shan Medical University, No. 110, Section 1, Jianguo N. Road, Taichung 402, Taiwan

6. Division of Gastroenterology, Department of Internal Medicine, Armed-Force Taichung General Hospital, Taichung 411, Taiwan

7. General Education Center, Central Taiwan University of Science and Technology, No. 11 Pu-tzu Lane, Pu-tzu Road, Taichung 406, Taiwan

8. Department of Pathology, Taichung Veterans General Hospital, Taichung 407, Taiwan

Abstract

Recent studies have revealed pleiotropic anticancer and antiproliferative capabilities ofDioscorea nipponicaMakino whereas the effect of this plant on metastasis of cancer cells has not been clearly clarified. In the present study, we extractedDioscorea nipponicaMakino with methanol (DNE1), chloroform (DNE2), ethyl acetate (DNE3),n-butanol (DNE4), and water (DNE5). We first demonstrate that DNE3 was found to be effective in reducing the lung metastases formation by about 99.5% as compared to vehicle-treated control animals. When a nontoxic concentration of the extract was treated directly to highly metastatic murin melanoma cells (B16F10) and human melanoma cells (A2058)in vitro, it exerted a dose-dependent inhibitory effect on the invasion(P<.001), motility(P<.001), secretion of MMPs(P<.001), and u-PA(P<.001)of both cell lines. To investigate the possible mechanisms involved in these events, we performed western blot analysis to find that DNE inhibited phosphorylation of Akt. A treatment with DNE3 to B16F10 cells also inhibited the activation of NF-κB and increased the expression of IkappaB. Taken together, these findings suggested that DNE3 could reduce the metastasis of melanoma cells, thereby constituting an adjuvant treatment for metastasis control.

Funder

National Science Council

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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