Transcription Factor E2F4 Promote Proliferation , Migration, and Invasion of Gastric Cancer Cells by DSCC1

被引:0
作者
Baral, Shantanu [1 ,2 ,3 ,4 ]
Yu, Yantao [4 ,6 ]
Sun, Qiannan [2 ,4 ]
Jiang, Mingrui [2 ,3 ,4 ]
Li, Ruiqi [4 ,5 ]
Cheng, Yifan [4 ,5 ]
Hussein, Arawker Mubeen [3 ]
Shi, Youquan [4 ]
Jiang, Yongjun [4 ]
Tang, Dong [2 ]
Wang, Sen [7 ]
Wang, Daorong [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Yangzhou Univ, Northern Jiangsu Peoples Hosp, Yangzhou 225001, Jiangsu, Peoples R China
[2] Northern Jiangsu Peoples Hosp, Yangzhou 225001, Jiangsu, Peoples R China
[3] Yangzhou Univ, Gen Surg Inst Yangzhou, Yangzhou 225001, Jiangsu, Peoples R China
[4] Yangzhou Key Lab Basic & Clin Transformat Digest &, Yangzhou 225001, Jiangsu, Peoples R China
[5] Nanjing Univ, Northern Jiangsu Peoples Hosp, Clin Teaching Hosp, Med Sch, Yangzhou 225001, Jiangsu, Peoples R China
[6] Dalian Med Univ, Yangzhou Sch Clin Med, Yangzhou 225001, Jiangsu, Peoples R China
[7] Nanjing Med Univ, Affiliated Hosp 1, Dept Gen Surg, Nanjing 210029, Jiangsu, Peoples R China
来源
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES | 2024年 / 20卷 / 12期
基金
中国国家自然科学基金;
关键词
Gastric Cancer; DNA Replication and Sister Chromatid Cohesion 1; Early; 2; Factor; 4; transcription; Proliferation; SISTER-CHROMATID COHESION; DNA-REPLICATION; PROGRESSION; EXPRESSION; PROGNOSIS;
D O I
10.7150/ijbs.99590
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
Gastric cancer (GC) ranks as the fifth most common cancer and the fourth leading cause of cancer-related deaths globally. Despite advancements in molecular profiling, the mechanisms driving GC proliferation and metastasis remain unclear. This study identifies Early 2 Factor 4 (E2F4) as a key transcription factor that promotes GC cell proliferation, migration, and invasion by upregulating DNA Replication and Sister Chromatid Cohesion 1 (DSCC1) expression. Bioinformatics and transcription factor analyses revealed E2F4 as a significant regulator of DSCC1. Functional assays confirmed E2F4's role in enhancing GC cell malignancy in vitro and in vivo. . Knockdown and overexpression experiments demonstrated that E2F4 positively regulates DSCC1 at the transcriptional level, with ChIP-qPCR and dual luciferase reporter assays validating the binding sites on the DSCC1 promoter. These findings highlight the E2F4-DSCC1 axis as a potential therapeutic target to mitigate GC progression.
引用
收藏
页码:4978 / 4998
页数:21
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