α-Pinene Inhibits Human Prostate Cancer Growth in a Mouse Xenograft Model

被引:66
作者
Zhao, Yunqi [1 ,2 ]
Chen, Ran [1 ,2 ]
Wang, Yun [1 ,2 ]
Yang, Yixin [3 ]
机构
[1] Kunming Med Univ, Sch Pharmaceut Sci, 1168 West Chun Rong Rd, Kunming 650500, Yunnan, Peoples R China
[2] Kunming Med Univ, Yunnan Prov Key Lab Pharmacol Nat Prod, 1168 West Chun Rong Rd, Kunming 650500, Yunnan, Peoples R China
[3] Kean Univ, Nathan Weiss Grad Coll, Union, NJ USA
关键词
alpha-Pinene; Prostate cancer; Apoptosis; Xenograft; CELL-LINES; ESSENTIAL OILS; CONSTITUENTS; PINUS;
D O I
10.1159/000479863
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: alpha-Pinene is one of the most widely found terpenoids in nature. Substantial evidence shows that a-pinene has cancer prevention properties. In this study, the PC-3 cell line was used to establish subcutaneous xenograft tumors in nude mice. Methods: Cytotoxicity was measured with the MTT assay, and apoptosis and cell cycle analyses were conducted using flow cytometry in vitro. The PC-3 cell line was used to establish subcutaneous xenograft tumors in nude mice. Results: We found that treatment with alpha-pinene significantly inhibited human prostate cancer cell growth and induced apoptosis and cell cycle arrest in the cell line-based model. Furthermore, tumor progression was inhibited more in mice treated with alpha-pinene than in control mice. We detected less Ki67 and proliferation cell nuclear antigen in paraffin sections from xenograft tumor specimens taken from a-pinene-treated mice than in those from the control group. Meanwhile, alpha-pinene treatment induced apoptosis in xenograft tumors as determined by the TUNEL assay. Conclusions: These data strongly suggest that alpha-pinene inhibits prostate cancer growth in a xenograft model and may be an effective therapeutic agent for prostate cancer treatment. (C) 2017 S. Karger AG, Basel
引用
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页码:1 / 7
页数:7
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