| Literature DB >> 28634077 |
Lin Huang1, Keng Chen1, Zhao-Peng Cai2, Fu-Chao Chen1, Hui-Yong Shen1, Wei-Hua Zhao3, Song-Jie Yang4, Xu-Biao Chen4, Guo-Xue Tang5, Xi Lin6.
Abstract
DEP domain containing 1 (DEPDC1) is recently reported to be overexpressed in several types of human cancer; however the role of DEPDC1 in prostate cancer remains to be investigated. Herein, we identified that the DEPDC1 mRNA and protein expression levels were dramatically increased in prostate cancer tissues and cell lines. Overexpression of DEPDC1 promoted, but depletion of DEPDC1 inhibited cell proliferation by regulating the G1-S phase cell cycle transition. Importantly, we found that DEPDC1 was essential for the tumor growth and formation of bone metastases of prostate cancer cells in vivo. Finally, we demonstrated that DEPDC1 interacted with E2F1 and increased its transcriptional activity, leading to hyper-activation of E2F signaling in prostate cancer cells. Our findings reveal an oncogenic role of DEPDC1 in prostate cancer progression via activation of E2F signaling, and suggest DEPDC1 might be a potential therapeutic target against the disease.Entities:
Keywords: Bone metastasis; Cell cycle; DEPDC1; E2F; Prostate cancer; Tumorigencity
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Year: 2017 PMID: 28634077 DOI: 10.1016/j.bbrc.2017.06.105
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575