木樨草素抑制蛋白激酶 C(epsilon)和 c-Src 的活性及 UVB 诱导的皮肤癌。
Luteolin inhibits protein kinase C(epsilon) and c-Src activities and UVB-induced skin cancer.
机构信息
Department of Agricultural Biotechnology, Major in Biomodulation, Seoul National University, Seoul, Republic of Korea.
出版信息
Cancer Res. 2010 Mar 15;70(6):2415-23. doi: 10.1158/0008-5472.CAN-09-4093. Epub 2010 Mar 9.
Luteolin, a flavonoid present in various vegetables including onion and broccoli, has been reported to possess anticarcinogenic effects. However, its chemopreventive effect on UV-induced skin cancer and its mechanism are not fully understood. Herein, we examined the chemopreventive effect and associated mechanisms of luteolin in the JB6 P+ cell line and the SKH-1 hairless mouse model. Luteolin suppressed UVB-induced cyclooxygenase-2 expression and activator protein-1 and nuclear factor-kappaB activity in JB6 P+ cells. Immunoblot and kinase assay data showed that luteolin attenuated protein kinase C(epsilon) (PKC(epsilon)) and Src kinase activities and subsequently inhibited UVB-induced phosphorylation of mitogen-activated protein kinases and the Akt signaling pathway. In addition, pull-down assays revealed that luteolin binds directly to PKC(epsilon) and Src in an ATP-competitive manner. Importantly, luteolin suppressed tumor incidence, multiplicity, and overall size in SKH-1 hairless mice. Analysis of the skin by immunohistochemistry and immunoblotting showed that luteolin-treated groups had a substantial reduction in the levels of cyclooxygenase-2, tumor necrosis factor-alpha, and proliferating cell nuclear antigen compared with groups treated with only UVB. Further analysis using skin lysates showed that luteolin inhibited PKC(epsilon) and Src kinase activity. Together, these data suggest that luteolin exerts potent chemopreventive activity against UVB-induced skin cancer mainly by targeting PKC(epsilon)and Src.
木犀草素是一种存在于洋葱和西兰花等各种蔬菜中的类黄酮,据报道具有抗癌作用。然而,其对紫外线诱导的皮肤癌的化学预防作用及其机制尚不完全清楚。在此,我们研究了木犀草素在 JB6 P+细胞系和 SKH-1 无毛小鼠模型中的化学预防作用及其相关机制。木犀草素抑制了 JB6 P+细胞中 UVB 诱导的环氧化酶-2 表达以及激活蛋白-1 和核因子-κB 活性。免疫印迹和激酶测定数据表明,木犀草素减弱了蛋白激酶 C(epsilon)(PKC(epsilon))和Src 激酶的活性,随后抑制了 UVB 诱导的丝裂原激活蛋白激酶和 Akt 信号通路的磷酸化。此外,下拉测定表明木犀草素以 ATP 竞争性方式直接与 PKC(epsilon)和 Src 结合。重要的是,木犀草素抑制了 SKH-1 无毛小鼠的肿瘤发生率、多发性和总体大小。免疫组织化学和免疫印迹分析显示,与仅用 UVB 处理的组相比,木犀草素处理组的环氧化酶-2、肿瘤坏死因子-α和增殖细胞核抗原水平显著降低。对皮肤裂解物的进一步分析表明,木犀草素抑制了 PKC(epsilon)和 Src 激酶的活性。总之,这些数据表明木犀草素通过靶向 PKC(epsilon)和 Src 对 UVB 诱导的皮肤癌发挥强大的化学预防作用。