FoXA2 promotes esophageal squamous cell carcinoma progression by ZEB2 activation

被引:10
|
作者
Gao, Hanjing [1 ]
Yan, Zheng [1 ]
Sun, Haiyan [2 ]
Chen, Yanfang [3 ]
机构
[1] Tianjin 4th Ctr Hosp, Dept Radiat Oncol, Tianjin 300140, Peoples R China
[2] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Tianjin Clin Res Ctr Canc, Dept Integrated Chinese & Western Med,Key Lab Can, Tianjin 300060, Peoples R China
[3] Tianjin Med Univ Second Hosp, Dept Radiat Oncol, 23 Pingjiang Rd, Tianjin 300211, Peoples R China
关键词
FOXA2; ESCC; Progression; ZEB2; EPITHELIAL-MESENCHYMAL TRANSITION; TARGETING ZEB2; CANCER; METASTASIS; SUPPRESSOR; FAMILY;
D O I
10.1186/s12957-021-02358-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background It has been reported that Forkhead transcription family member (FOXA2) regulates esophageal squamous cell carcinoma (ESCC) progression. However, the specific mechanism, by which FOXA2 promotes ESCC malignant progression, remains unclear. Materials and methods QRT-PCR and western blotting were applied to measure FOXA2 expression in ESCC tissues, while CCK-8 assay and Transwell assays were used to investigate the effect of FOXA2 on ESCC. Luciferase reporter assay, followed by fast chromatin immunoprecipitation (ChIP) assay, was used to study the relationship between FOXA2 and ZEB2. Results FOXA2 was significantly increased in ESCC tissues, when compared to normal tissues. Moreover, high expression of FOXA2 was also found in ESCC cells. Knockdown of FOXA2 inhibited ESCC cell proliferation, invasion, and migration. Mechanically, FOXA2 was verified to regulate ZEB2 expression at transcription level. Moreover, ZEB2 reversed the inhibitory effect of FOXA2 on ESCC proliferation, invasion, and migration. The relationship between ZEB2 and FOXA2 in ESCC tissues was negative. Conclusions These results indicate that FOXA2 plays a critical role in ESCC progression and may become a potential candidate target for ESCC treatment.
引用
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页数:10
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