Document Type
Article
Publication Date
6-15-2014
Abstract
Prostate cancer at advanced stages including metastatic and castration-resistant cancer remains incurable due to the lack of effective therapies. The CAMK2N1 gene, cloned and characterized as an inhibitor of CaMKII (calcium/calmodulin-dependent protein kinase II), has been shown to affect tumorigenesis and tumor growth. However, it is still unknown whether CAMK2N1 plays a role in prostate cancer development. We first examined the protein and mRNA levels of CAMK2N1 and observed a significant decrease in human prostate cancers comparing to normal prostate tissues. Re-expression of CAMK2N1 in prostate cancer cells reduced cellular proliferation, arrested cells in G0/G1 phases, and induced apoptotic cell death accompanied by down-regulation of IGF-1, ErbB2, and VEGF downstream kinases PI3K/AKT, as well as the MEK/ERK-mediated signaling pathways. Conversely, knockdown of CAMK2N1 had a significant opposite effects on these phenotypes. Our analyses suggest that CAMK2N1 plays a tumor suppressive role in prostate cancer cells. Reduced CAMK2N1 expression correlates to human prostate cancer progression and predicts poor clinical outcome, indicating that CAMK2N1 may serve as a biomarker. The inhibition of tumor growth by expressing CAMK2N1 established a role of CAMK2N1 as a therapeutic target.
Recommended Citation
Wang, Tao; Liu, Zhuo; Guo, Shuiming; Wu, Licheng; Li, Mingchao; Yang, Jun; Chen, Ruibao; Xu, Hua; Cai, Shaoxin; Chen, Hui; Li, Weiyong; Wang, Liang; Hu, Zhiquan; Zhuang, Qianyuan; Xu, Shaohua; Wang, Liping; Liu, Jihong; Ye, Zhangqun; Ji, Jun-Yuan; Wang, Chenguang; and Chen, Ke, "The tumor suppressive role of CAMK2N1 in castration-resistant prostate cancer." (2014). Department of Cancer Biology Faculty Papers. Paper 66.
https://jdc.jefferson.edu/cbfp/66
PubMed ID
25003983
Comments
This article has been peer reviewed. It was published in: Oncotarget. Volume 5, Issue 11, 2014, Pages 3611-3621.
The published version is available at http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path[]=1968. Copyright © Wang et. al.