Huang C, Bode A M, Chen N Y, Ma W Y, Li J, Nomura M, Dong Z
Hormel Institute, University of Minnesota, 801 16th Avenue NE, Austin, MN 55912, USA.
Anticancer Res. 2001 Jan-Feb;21(1A):261-7.
Arsenic is a recognized carcinogen, which acts as a tumor promoter rather than as an initiator. Signal transduction pathways leading to activation of AP-1 and mitogen-activated protein kinases are proposed to be responsible for the tumor promotion activity by arsenic. Induction of AP-1 DNA binding activity and c-jun and c-fos expression was reported to be only observed in cells responding to arsenite, but not to arsenate. However, in this study, we found that both arsenite and arsenate could induce transactivation of AP-1 in mouse epidermal JB6 AP-1-luciferase reporter stable transfectants, P+1-1. This induction of AP-1 activity by arsenic appears to be through activation of mitogen-activated protein kinases and protein kinase C because increased AP-1 activity by arsenite could be blocked by either treatment of cells with PD98059 or overexpression of dominant negative protein kinase Ca. Furthermore, both arsenite and arsenate could induce transactivation of AP-1 in AP-1-luciferase reporter transgenic mice.
砷是一种公认的致癌物,它作为肿瘤促进剂而非引发剂起作用。导致AP-1和丝裂原活化蛋白激酶激活的信号转导途径被认为是砷具有肿瘤促进活性的原因。据报道,AP-1 DNA结合活性以及c-jun和c-fos表达的诱导仅在对亚砷酸盐有反应的细胞中观察到,而对砷酸盐无反应。然而,在本研究中,我们发现亚砷酸盐和砷酸盐均可在小鼠表皮JB6 AP-1-荧光素酶报告基因稳定转染细胞P+1-1中诱导AP-1的反式激活。砷对AP-1活性的这种诱导似乎是通过丝裂原活化蛋白激酶和蛋白激酶C的激活实现的,因为用PD98059处理细胞或过表达显性负性蛋白激酶Ca均可阻断亚砷酸盐增加的AP-1活性。此外,亚砷酸盐和砷酸盐均可在AP-1-荧光素酶报告基因转基因小鼠中诱导AP-1的反式激活。