FOXM1 Promotes Malignant Proliferation of Esophageal Squamous Cell Carcinoma Through Transcriptional Activating CDC6

被引:7
|
作者
Chen, Xiongfeng [1 ]
Chen, Jingbo [2 ]
Yu, Xunbin [3 ]
Lin, Guishan [2 ,6 ]
Chen, Ting [1 ,4 ,5 ]
机构
[1] Fujian Med Univ, Sch Basic Med Sci, Dept Bioinformat, Fujian Key Lab Med Bioinformat,Key Lab Minist Educ, Fuzhou, Peoples R China
[2] Shengli Clin Med Coll Fujian Med Univ, Dept Oncol, Fuzhou, Peoples R China
[3] Shengli Clin Med Coll Fujian Med Univ, Fujian Prov Hosp, Dept Pathol, Fuzhou, Peoples R China
[4] Tsinghua Univ, Inst Artificial Intelligence, Dept Comp Sci & Technol, Beijing, Peoples R China
[5] Fujian Med Univ, Sch Basic Med Sci, Dept Bioinformat, Fujian Key Lab Med Bioinformat,Key Lab Minist Educ, Fuzhou 350122, Peoples R China
[6] Shengli Clin Med Coll Fujian Med Univ, Fujian Prov Hosp, Dept Oncol, Fuzhou 350001, Peoples R China
基金
中国国家自然科学基金;
关键词
FOXM1; CDC6; esophageal squamous cell carcinoma; tumor proliferation; POOR-PROGNOSIS; OVEREXPRESSION; EXPRESSION; CANCER;
D O I
10.1089/dna.2022.0169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Forkhead box M1 (FOXM1) is a proliferative transcription factor and plays a vital role in many cancers. However, the function and molecular mechanism of FOXM1 in esophageal squamous cell carcinoma (ESCC) remain poorly understood. Hence, we aim to clarify the molecular basis of FOXM1-mediated ESCC progression. In this study, bioinformatics analysis showed that FOXM1 was mainly involved in key signal pathways, including cell proliferation, cell cycle, and homologous recombination in ESCC, and predicted that CDC6 might be a potential regulatory target gene of FOXM1. The results revealed that FOXM1 and CDC6 were significantly overexpressed in ESCC tissue and cell line, and their expression was positively correlated. Further studies showed that FOXM1 directly transcriptionally activated CDC6 by binding to its promoter region in ESCC cells. Moreover, FOXM1 mediated ESCC cell proliferation by regulating CDC6 expression, which may be related to promoting G1-S phase transition of cell cycle. Taken together, FOXM1-CDC6 axis mediates ESCC malignant proliferation and may serve as a potential biological target for ESCC treatment.
引用
收藏
页码:671 / 682
页数:12
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