Licato L L, Brenner D A
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, 27599, USA.
Dig Dis Sci. 1998 Jul;43(7):1454-64. doi: 10.1023/a:1018894227169.
Extracellular signal-related kinase (ERK) and c-Jun N-terminal kinase (JNK) mitogen-activated protein (MAP) kinases are highly activated in an in vivo rat model of colorectal carcinogenesis. In addition, other protein kinases such as c-Src and c-Yes have been shown to be up-regulated in some human colon cancers. To evaluate the activity of these kinases in human colorectal carcinomas, we examined colon cancers and adjacent normal intestinal mucosa from 11 patients. Moderate increases in ERK and JNK activities, in addition to up-regulation of c-Src, p125FAK, and tyrosine-phosphorylated proteins, were observed in a subset of the colorectal carcinomas. There was a significant correlation found between levels of c-Src, p125FAK, and tyrosine-phosphorylated proteins, as well as between c-Src protein levels and JNK activity. This is the first report that examines several different kinases as markers to characterize colorectal cancers in the same carcinoma sample, allowing the determination of correlations between markers in the same tumors.
细胞外信号调节激酶(ERK)和c-Jun氨基末端激酶(JNK)丝裂原活化蛋白(MAP)激酶在大鼠结直肠癌发生的体内模型中被高度激活。此外,其他蛋白激酶,如c-Src和c-Yes,已被证明在一些人类结肠癌中上调。为了评估这些激酶在人类结直肠癌中的活性,我们检测了11例患者的结肠癌组织和相邻的正常肠黏膜。在一部分结肠癌中,观察到ERK和JNK活性适度增加,同时c-Src、p125FAK和酪氨酸磷酸化蛋白上调。在c-Src、p125FAK和酪氨酸磷酸化蛋白水平之间,以及c-Src蛋白水平和JNK活性之间发现了显著相关性。这是第一份在同一癌组织样本中检测几种不同激酶作为结直肠癌特征标志物的报告,从而能够确定同一肿瘤中标志物之间的相关性。