Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma

被引:9
作者
Cao, Ji-Xiang [1 ,2 ]
Lu, Yao [3 ]
机构
[1] Peking Univ, Sch Life Sci, Key Lab Cell Proliferat & Differentiat, Minist Educ, Beijing 100871, Peoples R China
[2] Xiamen Univ, Dept Pathol, Zhongshan Hosp, Xiamen 361004, Peoples R China
[3] Peking Univ, Hosp 3, Dept Rehabil Med, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
CDC7; ESCC; chemosensitivity; therapeutic target; proliferation; migration and invasion; THERAPEUTIC TARGET; CANCER; KINASE; CHEMORESISTANCE; REPLICATION; SURVIVAL; POTENT; FIBROBLASTS; ACTIVATION; RESISTANCE;
D O I
10.2147/OTT.S183629
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Purpose: The cell division cycle 7 (CDC7) is a serine/threonine kinase that is essential for DNA replication in human cells which has been identified to play a critical role in multiple cancer types. However, the expression and clinical significance of CDC7 in ESCC has never been reported. Patients and methods: CDC7 expression was detected in 30 ESCC and matched adjacent normal tissues, and a series of loss-of-function and gain-of-function assays were performed to evaluate the effects of CDC7 on the proliferation, migration and invasion, and chemoresistance of ESCC cells. Results: The results showed that CDC7 was highly expressed in ESCC tissues compared with matched adjacent normal tissues. Functional studies demonstrated that knockdown of CDC7 inhibited proliferation by arresting ESCC cells in the G0/G1 phase and inducing apoptosis. Knockdown of CDC7 also inhibited cell migration and invasion in ESCC cells. Furthermore, knockdown of CDC7 sensitized ESCC cells to Cis and 5-FU. Conclusion: Our results suggest that CDC7 is highly expressed in ESCC tissues, and silencing CDC7 enhances chemosensitivity of ESCC cells, providing a new avenue for ESCC therapy.
引用
收藏
页码:63 / 74
页数:12
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