Notoginseng enhances anti-cancer effect of 5-fluorouracil on human colorectal cancer cells

被引:102
|
作者
Wang, Chong-Zhi
Luo, Xiaoji
Zhang, Bin
Song, Wen-Xin
Mehendale, Sangeeta
Xie, Jing-Tian
Aung, Han H.
He, Tong-Chuan
Yuan, Chun-Su
机构
[1] Univ Chicago, Tang Ctr Herbal Med Res, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Anesthesia & Crit Care, Chicago, IL 60637 USA
[3] Univ Chicago, Med Ctr, Dept Surg, Mol Oncol Lab, Chicago, IL 60637 USA
[4] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[6] Univ Chicago, Comm Clin Pharmacol & Pharmacogenom, Chicago, IL 60637 USA
关键词
Panax notoginseng; 5-fluorouracil; chemotherapy; HCT-116 human colorectal cancer cells; anti-proliferation; apoptosis;
D O I
10.1007/s00280-006-0350-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Panax notoginseng is a commonly used Chinese herb. Although a few studies have found that notoginseng shows anti-tumor effects, the effect of this herb on colorectal cancer cells has not been investigated. 5-Fluorouracil (5-FU) is a chemotherapeutic agent for the treatment of colorectal cancer that interferes with the growth of cancer cells. However, this compound has serious side effects at high doses. In this study, using HCT-116 human colorectal cancer cell line, we investigated the possible synergistic anti-cancer effects between notoginseng flower extract (NGF) and 5-FU on colon cancer cells. Methods The anti-proliferation activity of these modes of treatment was evaluated by MTS cell proliferation assay. Apoptotic effects were analyzed by using Hoechst 33258 staining and Annexin-V/PI staining assays. The anti-proliferation effects of four major single compounds from NGF, ginsenosides Rb1, Rb3, Rc and Rg3 were also analyzed. Results Both 5-FU and NGF inhibited proliferation of HCT-116 cells. With increasing doses of 5-FU, the anti-proliferation effect was slowly increased. The combined usage of 5-FU 5 mu M and NGF 0.25 mg/ml, significantly increased the anti-proliferation effect (59.4 +/- 3.3%) compared with using the two medicines separately (5-FU 5 mu M, 31.1 +/- 0.4%; NGF 0.25 mg/ml, 25.3 +/- 3.6%). Apoptotic analysis showed that at this concentration, 5-FU did not exert an apoptotic effect, while apoptotic cells induced by NGF were observed, suggesting that the anti-proliferation target(s) of NGF may be different from that of 5-FU, which is known to inhibit thymidilate synthase. Conclusions This study demonstrates that NGF can enhance the anti-proliferation effect of 5-FU on HCT-116 human colorectal cancer cells and may decrease the dosage of 5-FU needed for colorectal cancer treatment.
引用
收藏
页码:69 / 79
页数:11
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