Department of Anatomy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
PLoS One. 2012;7(7):e42210. doi: 10.1371/journal.pone.0042210. Epub 2012 Jul 31.
CDK5 regulatory subunit associated protein 3 (CDK5RAP3) is a novel activator of PAK4 and processes important pro-metastatic function in hepatocarcinogenesis. However, it remains unclear if there are other mechanisms by which CDK5RAP3 promotes HCC metastasis. Here, we showed that in CDK5RAP3 stable knockdown SMMC-7721 HCC cells, p14(ARF) tumor suppressor was upregulated at protein and mRNA levels, and ectopic expression of CDK5RAP3 was found to repress the transcription of p14(ARF). Using chromatin immunoprecipitation assay, we demonstrated that CDK5RAP3 bound to p14(ARF) promoter in vivo. Furthermore, knockdown of p14(ARF) in CDK5RAP3 stable knockdown HCC cells reversed the suppression of HCC cell invasiveness mediated by knockdown of CDK5RAP3. Taken together, our findings provide the new evidence that overexpression of CDK5RAP3 promotes HCC metastasis via downregulation of p14(ARF).
CDK5 调节亚基相关蛋白 3(CDK5RAP3)是 PAK4 的新型激活剂,在肝癌发生中具有重要的促转移功能。然而,CDK5RAP3 是否还有其他促进 HCC 转移的机制尚不清楚。在这里,我们发现 CDK5RAP3 稳定敲低的 SMMC-7721 HCC 细胞中,p14(ARF)肿瘤抑制因子在蛋白质和 mRNA 水平上上调,并且发现 CDK5RAP3 的异位表达抑制了 p14(ARF)的转录。通过染色质免疫沉淀实验,我们证明 CDK5RAP3 在体内与 p14(ARF)启动子结合。此外,在 CDK5RAP3 稳定敲低的 HCC 细胞中敲低 p14(ARF),逆转了 CDK5RAP3 敲低介导的 HCC 细胞侵袭性的抑制。总之,我们的研究结果提供了新的证据,表明 CDK5RAP3 的过表达通过下调 p14(ARF)促进 HCC 转移。