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ZEB1: Catalyst of immune escape during tumor metastasis

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 153, 期 -, 页码 -

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.113490

关键词

ZEB1; EMT; Signaling pathway; Metastasis; Tumor immunity

资金

  1. Wuxi Health Care Commission Double Hundred Top Talent
  2. [BJ2020013]

向作者/读者索取更多资源

ZEB1, a critical transcription factor in tumor metastasis, is regulated by various pathways and molecules and influences tumor cell movement, stemness, and immune environment, providing new insights for targeted therapy of malignant tumors.
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.

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