Cyclin-dependent kinase 3-mediated activating transcription factor 1 phosphorylation enhances cell transformation

Duo Zheng, Yong Yeon Cho, Andy T.Y. Lau, Jishuai Zhang, Wei-Ya Ma, Ann M. Bode, Zigang Dong

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

Cyclin-dependent kinase (cdk)-3, a member of the cdk family of kinases, plays a critical role in cell cycle regulation and is involved in G 0-G1 and G1-S cell cycle transitions. However, the role of cdk3 in cell proliferation, as well as cell transformation, is not yet clearly understood. Here, we report that the protein expression level of cdk3 is higher in human cancer cell lines and human glioblastoma tissue compared with normal brain tissue. Furthermore, we found that cdk3 phosphorylates activating transcription factor 1 (ATF1) at serine 63 and enhances the transactivation and transcriptional activities of ATF1. Results also indicated that siRNA directed against cdk3 (si-cdk3) suppresses ATF1 activity, resulting in inhibition of proliferation and growth of human glioblastoma T98G cells in soft agar. Importantly , we showed that cdk3 enhances epidermal growth factor-induced transformation of JB6 Cl41 cells and si-cdk3 suppresses Ras G12V/cdk3/ATF1-induced foci formation in NIH3T3 cells. These results clearly showed that the cdk3-ATF1 signaling axis is critical for cell proliferation and transformation.

Original languageEnglish (US)
Pages (from-to)7650-7660
Number of pages11
JournalCancer Research
Volume68
Issue number18
DOIs
StatePublished - Sep 15 2008

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