标题:Cyclin-Dependent Kinase Inhibitor 3 Promoted Cell Proliferation by Driving Cell Cycle from G1 to S Phase in Esophageal Squamous Cell Carcinoma
作者:Liu, Juan; Min, Li; Zhu, Shengtao; Guo, Qingdong; Li, Hengcun; Zhang, Zheng; Zhao, Yu; Xu, Changqin; Zhang, Shutian
作者机构:[Liu, Juan; Min, Li; Zhu, Shengtao; Guo, Qingdong; Li, Hengcun; Zhang, Zheng; Zhao, Yu; Zhang, Shutian] Capital Med Univ, Beijing Friendship Hosp, Bei 更多
通讯作者:Zhang, ST;Xu, CQ
通讯作者地址:[Zhang, ST]Capital Med Univ, Beijing Friendship Hosp, Beijing Key Lab Precanc Les Digest Dis,Dept Gastr, Beijing Digest Dis Ctr,Natl Clin Res Ctr Dige 更多
来源:JOURNAL OF CANCER
出版年:2019
卷:10
期:8
页码:1915-1922
DOI:10.7150/jca.27053
关键词:ESCC; CDKN3; cell cycle; G1/S transition; cyclinD-CDK4 complex
摘要:Background and aims. Cyclin-dependent kinase inhibitor 3 (CDKN3) has been found playing a varying role in carcinogenesis, but its biological function in esophageal squamous cell carcinoma (ESCC) is unclear. The aim of this study was to demonstrate the role of CDKN3 in ESCC.; Materials and Methods: Real-time PCR and Western blot was performed in 15 pairs of ESCC tissues and adjacent normal esophageal tissues. Then cell proliferation ability, cloning ability, cell cycle status and migration and invasion ability were explored in CDKN3 overexpressed TE1 cell line and CDKN3 siRNA transfected TE1 and KYSE70 cell lines. Finally, cell cycle related proteins CyclinD1, CDK4, pAKT, P53, P21, and P27 were tested by Western blot.; Results: mRNA level was higher in 11 ESCC tissues compared to adjacent normal tissues, and an increased protein expression was further detected in 8 of those 11 ESCC tissues. Functional assays showed that CDKN3 overexpression promoted ESCC cell proliferation, colony formation, migration and invasion, and facilitated G1/S transition. Opposite results were also got after transfected with CDKN3 siRNA. Cell cycle associated protein pAKT, CyclinD1, CDK4 and P27 were upregulated and P53, P21 and were downregulated under CDKN3 overexpression. All the protein levels were found changed in the opposite direction when CDKN3 expression was disturbed by siRNA.; Conclusions: Our study suggested that CDKN3 acted as an oncogene in human ESCC and may accelerate the G1/S transition by affecting CyclinD-CDK4 complex via regulating pAKT-p53-p21 axis and p27 independent of AKT.
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85067306867&doi=10.7150%2fjca.27053&partnerID=40&md5=6db412ebf34786c81df1f18daf95eb4b
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