Ma W Y, Huang C, Dong Z
The Hormel Institute, University of Minnesota, Austin, Minnesota 55912, USA.
Int J Oncol. 1998 Mar;12(3):565-8. doi: 10.3892/ijo.12.3.565.
The exposure of mammalian cells to ultraviolet (UV) irradiation leads to the activation of transcription factors, such as AP-1 and NFkB. We demonstrate that aspirin, a promising cancer chemopreventative agent, inhibited UVC-induced AP-1 activity in JB6 cells. In JB6 cells, UVC stimulated Erks, JNKs and P38 kinase activities; aspirin only inhibited activation of JNKs, but not the other MAP kinases. Since the transcription factor AP-1 is important for the process of tumor promotion, the inhibitory effect of aspirin on AP-1 activation suggests that it can be used as a chemopreventative agent against skin cancer.
哺乳动物细胞暴露于紫外线(UV)照射下会导致转录因子如AP-1和NFkB的激活。我们证明,阿司匹林作为一种有前景的癌症化学预防剂,可抑制JB6细胞中紫外线C(UVC)诱导的AP-1活性。在JB6细胞中,UVC刺激了细胞外信号调节激酶(Erks)、应激活化蛋白激酶(JNKs)和p38激酶的活性;阿司匹林仅抑制JNKs的激活,而不影响其他丝裂原活化蛋白激酶(MAP激酶)。由于转录因子AP-1在肿瘤促进过程中很重要,阿司匹林对AP-1激活的抑制作用表明它可作为预防皮肤癌的化学预防剂。