4.7 Article

Antiproliferative Effects of Different Plant Parts of Panax notoginseng on SW480 Human Colorectal Cancer Cells

期刊

PHYTOTHERAPY RESEARCH
卷 23, 期 1, 页码 6-13

出版社

WILEY
DOI: 10.1002/ptr.2383

关键词

Panax notoginseng; HPLC analysis; anticancer; cell cycle; apoptosis; SW480 human colorectal cancer cells

资金

  1. NIH/NCCAM [AT004418, AT003255]
  2. NIH/NCI [CA106569]
  3. American Cancer Society [RSG-05-254-01 DDC]
  4. NATIONAL CANCER INSTITUTE [R01CA106569] Funding Source: NIH RePORTER
  5. NATIONAL CENTER FOR COMPLEMENTARY & ALTERNATIVE MEDICINE [P01AT004418] Funding Source: NIH RePORTER
  6. NATIONAL CENTER FOR COMPLEMENTARY &ALTERNATIVE MEDICINE [R21AT002445, R21AT003255] Funding Source: NIH RePORTER

向作者/读者索取更多资源

The chemical constituents anti antiproliferative effects on SW480 human colorectal cancer cells of different plant parts of P. nologinseng were evaluated. The contents of saponins in extracts from root, rhizome, flower and berry of P. notoginseng were determined using high performance liquid chromatography. The contents and proportions of saponins were different among the four plant parts. Using the cell counting method, the antiproliferative effects were evaluated and the results indicated all four extracts, at 0.05-1.0 mg/mL, showed concentration-related antiproliferative effects oil the cancer cells. The flower extract had stronger effects compared with the other three extracts; at 1.0 mg/mL, it inhibited the cell growth by 93.1% (p < 0.01). The antiproliferative effects of major saponins in nologinseng, notoginsenoside R1, ginsenosides Rb1, Rb3 and Rg1, were also evaluated, and the observed effects of major constituents support the pharmacological activities of extracts. The effects of notoginseng extracts oil cell cycle and apoptosis of SW480 cells were determined using flow cytometry. Notoginseng extract can arrest the cells in S anti G2/M phases. Remarkably apoptosis induction activities of notoginseng extracts were observed with the flower extract possessing the most potent effect, supporting the antiproliferative effect. Copyright (c) 2008 John Wiley & Sons, Ltd.

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