Park In-Ja, Hwang Jin-Taek, Kim Young Min, Ha Joohun, Park Ock Jin
Department of Food and Nutrition, Hannam University, 133 Ojeong-dong Daedeok-gu, Daejeon 306-791, Korea.
Ann N Y Acad Sci. 2006 Dec;1091:102-9. doi: 10.1196/annals.1378.059.
This study was undertaken to examine the effect of low and high concentrations of H2O2 on cancer cell proliferation and apoptosis, and AMPK signaling pathways in HT-29 human colon cancer cells. Nontoxic doses of H2O2 (10 microM) induced cancer cell proliferation, whereas the toxic level of 1,000 microM H2O2 induced apoptosis. The stimulation of cell proliferation was accompanied with an increase in cyclooxygenase-2 (COX-2), and apoptosis induced by high-dose H2O2 was correlated with the activation of AMPK and negatively correlated with COX-2 expression. These results suggest that ROS at nontoxic levels can stimulate cancer cell growth by regulating AMP-activated protein kinase (AMPK) and/or COX-2, and the abundant exogenous ROS linked to the growth inhibition through modulating AMPK signaling pathways.
本研究旨在探讨低浓度和高浓度过氧化氢(H2O2)对HT-29人结肠癌细胞增殖、凋亡及AMPK信号通路的影响。无毒剂量的H2O2(10微摩尔)诱导癌细胞增殖,而1000微摩尔H2O2的毒性水平则诱导细胞凋亡。细胞增殖的刺激伴随着环氧化酶-2(COX-2)的增加,高剂量H2O2诱导的凋亡与AMPK的激活相关,与COX-2表达呈负相关。这些结果表明,无毒水平的活性氧(ROS)可通过调节AMP激活蛋白激酶(AMPK)和/或COX-2来刺激癌细胞生长,而大量外源性ROS则通过调节AMPK信号通路与生长抑制相关。