ZEB1: Catalyst of immune escape during tumor metastasis

被引:15
|
作者
Lu, Jiahui [1 ]
Fei, Fei [1 ]
Wu, Chenxi [1 ]
Mei, Jie [1 ]
Xu, Junying [1 ,2 ]
Lu, Peihua [1 ,2 ]
机构
[1] Nanjing Med Univ, Wuxi Peoples Hosp, Dept Oncol, Wuxi 214023, Peoples R China
[2] Nanjing Med Univ, Wuxi Peoples Hosp, Dept Oncol, 299 Qingyang Rd, Wuxi 214023, Peoples R China
关键词
ZEB1; EMT; Signaling pathway; Metastasis; Tumor immunity; EPITHELIAL-MESENCHYMAL TRANSITION; EMT-ACTIVATOR ZEB1; GRAINYHEAD-LIKE; CANCER-CELLS; ZINC-FINGER; COLORECTAL-CANCER; SIGNALING PATHWAY; DOWN-REGULATION; TARGETING ZEB1; LUNG-CANCER;
D O I
10.1016/j.biopha.2022.113490
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The transcription factor zinc finger E-box binding homeobox 1 (ZEB1) is a critical inducer of epithelial mesenchymal transformation (EMT) and plays a robust role in tumor metastasis. It can promote not only the movement and diffusion of tumor cells but also cell stemness, treatment resistance, tumor metastasis and immune escape. The expression of ZEB1 is strictly regulated by a variety of pretranscriptional and posttranscriptional signaling pathways and molecules. Increasing evidence indicates that protein modifications such as methylation and acetylation of ZEB1 can also affect tumor metastasis. More importantly, ZEB1 induces immunosuppressive cells and chemokines into the tumor microenvironment (TME), leading to the formation of a tumor immunosuppressive microenvironment. This review summarizes the regulatory factors involved in ZEB1 expression and its important role. The areas of research covered in this review contribute to providing new thoughts and new treatment insights for targeted ZEB1 therapy of malignant tumors.
引用
收藏
页数:9
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