Seo Woon-Gyo, Hwang Jae-Cheol, Kang Sung-Koo, Jin Un-Ho, Suh Seok-Jong, Moon Sung-Kwon, Kim Cheorl-Ho
Department of Biochemistry, Molecular Biology and Internal Medicine, College of Oriental Medicine, Dongguk University and National Research Laboratory for Glycobiology, Sukjang-Dong 707, Kyungju City, Kyungbuk 780-714, Republic of Korea.
J Ethnopharmacol. 2005 Oct 3;101(1-3):249-57. doi: 10.1016/j.jep.2005.04.037.
The inhibitory effect of Curcuma zedoaria Roscoe (WE-CZ) on experimental pulmonary metastasis of B16 melanoma cells was investigated. The intake of WE-CZ at doses of 250 and 500 mg/kg for 6 weeks from 2 weeks before tumor inoculation significantly reduced the number of metastatic surface nodules in the lung, resulting in an extended life span. When the duration of WE-CZ intake was examined, survival time was not affected by pre-intake before B16 melanoma cell inoculation and was slightly extended by post-intake after B16 melanoma cell inoculation, although the life span was prolonged by intake throughout the experiment. To address the mechanism underlying the anti-metastatic effect of WE-CZ, we examined the issue of whether WE-CZ modulated macrophage function, which is involved in killing tumor cells. The intake of WE-CZ for 6 weeks increased nitric oxide (NO) production by macrophages following stimulation with lipopolysaccharide in a dose-dependent manner. The elevated NO was found to serve as a cytotoxic mediator against B16 melanoma cells in co-culture with macrophages. On the contrary, B16 melanoma-conditioned medium reduced NO production by macrophages. However, WE-CZ treatment significantly reversed the reduction in NO production by the conditioned medium. These findings indicate that WE-CZ possesses anti-migratory effects on B16 melanoma cells and that the macrophage function-modulating activity by WE-CZ appears to underlie its anti-metastatic activity, which leads to a decrease in the number of lung metastatic surface nodules and the extension of life span. These results suggest that WE-CZ may play important roles in the inhibition of cancer metastasis.
研究了莪术(WE-CZ)对B16黑色素瘤细胞实验性肺转移的抑制作用。从肿瘤接种前2周开始,以250和500 mg/kg的剂量摄入WE-CZ,持续6周,可显著减少肺转移表面结节的数量,从而延长生存期。当检查WE-CZ的摄入持续时间时,在接种B16黑色素瘤细胞之前摄入对生存时间没有影响,而在接种B16黑色素瘤细胞之后摄入则可使生存时间略有延长,尽管在整个实验过程中摄入均可延长生存期。为了探讨WE-CZ抗转移作用的潜在机制,我们研究了WE-CZ是否调节参与杀伤肿瘤细胞的巨噬细胞功能这一问题。摄入WE-CZ 6周后,脂多糖刺激的巨噬细胞一氧化氮(NO)生成量呈剂量依赖性增加。在与巨噬细胞共培养时,升高的NO被发现可作为针对B16黑色素瘤细胞的细胞毒性介质。相反,B16黑色素瘤条件培养基可降低巨噬细胞的NO生成。然而,WE-CZ处理可显著逆转条件培养基导致的NO生成减少。这些发现表明,WE-CZ对B16黑色素瘤细胞具有抗迁移作用,并且WE-CZ调节巨噬细胞功能的活性似乎是其抗转移活性的基础,这导致肺转移表面结节数量减少和生存期延长。这些结果表明,WE-CZ可能在抑制癌症转移中发挥重要作用。