SOX2
转录因子
生物
癌症干细胞
同源盒蛋白纳米
癌症研究
癌变
泛素
KLF4公司
转移
泛素连接酶
细胞生物学
癌症
干细胞
诱导多能干细胞
遗传学
胚胎干细胞
基因
作者
Weijia Wang,Wenjun Liu,Qiuli Chen,Yong Yuan,Peter Wang
标识
DOI:10.1016/j.semcancer.2022.11.002
摘要
Evidence has revealed that transcription factors play essential roles in regulation of multiple cellular processes, including cell proliferation, metastasis, EMT, cancer stem cells and chemoresistance. Dysregulated expression levels of transcription factors contribute to tumorigenesis and malignant progression. The expression of transcription factors is tightly governed by several signaling pathways, noncoding RNAs and E3 ubiquitin ligases. Cancer stem cells (CSCs) have been validated in regulation of tumor metastasis, reoccurrence and chemoresistance in human cancer. Transcription factors have been verified to participate in regulation of CSC formation, including Oct4, SOX2, KLF4, c-Myc, Nanog, GATA, SALL4, Bmi-1, OLIG2, POU3F2 and FOX proteins. In this review article, we will describe the critical role of CSC-related transcription factors. We will further discuss which E3 ligases regulate the degradation of these CSC-related transcription factors and their underlying mechanisms. We also mentioned the functions and mechanisms of EMT-associated transcription factors such as ZEB1, ZEB2, Snail, Slug, Twist1 and Twist2. Furthermore, we highlight the therapeutic potential via targeting E3 ubiquitin ligases for modulation of these transcription factors.
科研通智能强力驱动
Strongly Powered by AbleSci AI