Plakophilin 3 oncogene as prognostic marker and therapeutic target for lung cancer

被引:108
作者
Furukawa, C
Daigo, Y
Ishikawa, N
Kato, T
Ito, T
Tsuchiya, E
Sone, S
Nakamura, Y
机构
[1] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Mol Med Lab,Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokushima, Sch Med, Dept Internal Med & Mol Therapeut, Tokushima 770, Japan
[3] Hokkaido Univ Hosp, Dept Surg Pathol, Sapporo, Hokkaido 060, Japan
[4] Kanagawa Canc Ctr, Res Inst, Kanagawa, Japan
关键词
D O I
10.1158/0008-5472.CAN-04-1877
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated gene expression profiles of non-small cell lung carcinomas (NSCLC) to screen candidate molecules that might be useful as diagnostic markers or for development of novel molecular-targeting therapies. Here we report evidence that a member of the armadillo protein family, plakophilin 3 (PKP3), is a potential molecular target for treatment of lung cancers and might also serve as a prognostic indicator. We documented elevated expression of PKP3 in the great majority of NSCLC samples examined. Treatment of NSCLC cells with small interfering RNAs of PKP3 suppressed growth of the cancer cells; on the other hand, induction of exogenous expression of PKP3 conferred growth-promoting activity on COS-7 cells and enhanced their mobility in vitro. To investigate its function, we searched for PKP3-interacting proteins and identified dynamin I-like, which was also activated in NSCLC. In addition, a high level of PKP3 expression was associated with poor survival as well as disease stage and node status for patients with lung adenocarcinoma, suggesting an important role of the protein in development and progression of this disease. As our data imply that up-regulation of PKP3 is a frequent and important feature of lung carcinogenesis, we suggest that targeting the PKP3 molecule might hold promise for development of a new therapeutic and diagnostic strategy for clinical management of lung cancers.
引用
收藏
页码:7102 / 7110
页数:9
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