AURKA is one of the downstream targets of MAPK1/ERK2 in pancreatic cancer

被引:106
作者
Furukawa, T.
Kanai, N.
Shiwaku, H. O.
Soga, N.
Uehara, A.
Horii, A.
机构
[1] Tokyo Womens Med Univ, Int Res & Educ Inst Integrated Med Sci, Shinjuku Ku, Tokyo 1628666, Japan
[2] Tohoku Univ, Sch Med, Dept Mol Pathol, Sendai, Miyagi 980, Japan
关键词
aurora; gene expression; kinase; microarray; phosphatase; signal transduction;
D O I
10.1038/sj.onc.1209494
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DUSP6/MKP-3, a specific inhibitor of MAPK1/ERK2, frequently loses its expression in primary pancreatic cancer tissues. This evidence suggests that constitutive activation of MAPK1 synergistically induced by frequent mutation of KRAS2 and the loss of function of DUSP6 plays key roles in pancreatic carcinogenesis and progression. By pro. ling of gene expressions associated with downregulation of MAPK1 induced by exogenous overexpression of DUSP6 in pancreatic cancer cells, we found that AURKA/STK15, the gene encoding Aurora-A kinase, which plays key roles in cellular mitosis, was among the downregulated genes along with its related genes, which included AURKB, TPX2 and CENPA. An association of expression and promoter activity of AURKA with MAPK activity was verified. Knockdown of ETS2 resulted in a reduction of AURKA expression. These results indicate that AURKA is a direct target of the MAPK pathway and that its overexpression in pancreatic cancer is induced by hyperactivation of the pathway, at least via ETS2.
引用
收藏
页码:4831 / 4839
页数:9
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