Cao Ji-Xiang, Lu Yao
Key Laboratory of Cell Proliferation and Differentiation of the Ministry of Education, School of Life Science, Peking University, Beijing 100871, People's Republic of China,
Department of Pathology, Zhongshan Hospital Xiamen University, Xiamen 361004, People's Republic of China,
Onco Targets Ther. 2018 Dec 20;12:63-74. doi: 10.2147/OTT.S183629. eCollection 2019.
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.
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.
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.
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.
细胞分裂周期7(CDC7)是一种丝氨酸/苏氨酸激酶,对人类细胞中的DNA复制至关重要,已被确定在多种癌症类型中起关键作用。然而,CDC7在食管鳞状细胞癌(ESCC)中的表达及临床意义尚未见报道。
检测了30例ESCC组织及其配对的癌旁正常组织中CDC7的表达,并进行了一系列功能缺失和功能获得实验,以评估CDC7对ESCC细胞增殖、迁移、侵袭及化疗耐药性的影响。
结果显示,与配对的癌旁正常组织相比,CDC7在ESCC组织中高表达。功能研究表明,敲低CDC7可通过使ESCC细胞停滞于G0/G1期并诱导凋亡来抑制增殖。敲低CDC7还可抑制ESCC细胞的迁移和侵袭。此外,敲低CDC7可使ESCC细胞对顺铂和5-氟尿嘧啶敏感。
我们的结果表明,CDC7在ESCC组织中高表达,沉默CDC7可增强ESCC细胞的化疗敏感性,为ESCC治疗提供了新途径。