Tseng Ya-Shih, Tzeng Ching-Cherng, Huang Chi-Ying F, Chen Ping-Hong, Chiu Allen Wen-Hsiang, Hsu Pei-Yin, Huang Guan-Cheng, Wang Yu-Chun, Liu Hsiao-Sheng
College of Medicine, Institute of Basic Medical Sciences, National Cheng Kung University, Tainan, Taiwan, ROC.
Cancer Lett. 2006 Sep 8;241(1):93-101. doi: 10.1016/j.canlet.2005.10.014. Epub 2005 Dec 9.
Our data revealed that 59.4% of the bladder cancer specimens showed Aurora-A overexpression, of which 31.8% also had Ha-ras codon-12 mutation; 45.5% were from blackfoot-disease endemic areas in which arsenic exposure is a major environment factor associated with various cancer formation. We further demonstrated that arsenic treatment of the immortalized bladder cell line, E7, increased Aurora-A expression. All together, co-existence of Aurora-A overexpression and Ha-ras mutation suggests a possible additively effect on the tumorigenesis of bladder cancer. In addition, Aurora-A overexpression and up-regulated by arsenic exposure opens a new direction for exploring the occurrence of bladder cancer occurrence in Taiwan.
我们的数据显示,59.4%的膀胱癌标本呈现Aurora-A过表达,其中31.8%同时伴有Ha-ras密码子12突变;45.5%来自乌脚病流行地区,在这些地区,砷暴露是与各种癌症形成相关的主要环境因素。我们进一步证明,用砷处理永生化膀胱细胞系E7可增加Aurora-A的表达。总之,Aurora-A过表达与Ha-ras突变并存提示其对膀胱癌发生可能具有累加效应。此外,Aurora-A过表达且受砷暴露上调为探索台湾地区膀胱癌的发生开辟了新方向。