小RNA
信使核糖核酸
癌症研究
血管生成
癌症
小发夹RNA
RNA剪接
核糖核酸
选择性拼接
生物
癌细胞
癌变
基因
遗传学
作者
Jiawei Yang,Chao Sun,Jin Qiuyang,Xing-Hui Qiao,Xiu-Li Guo
出处
期刊:Current Cancer Drug Targets
[Bentham Science]
日期:2021-12-01
卷期号:21 (11): 897-906
被引量:2
标识
DOI:10.2174/1568009621666210831125001
摘要
As one of the most conservative proteins in evolution, Y-box-binding protein 1 (YB-1) has long been considered as a potential cancer target. YB-1 is usually poorly expressed in normal cells and exerts cellular physiological functions such as DNA repair, pre-mRNA splicing and mRNA stabilizing. In cancer cells, the expression of YB-1 is up-regulated and undergoes nuclear translocation and contributes to tumorigenesis, angiogenesis, tumor proliferation, invasion, migration and chemotherapy drug resistance. During the past decades, a variety of pharmacological tools such as siRNA, shRNA, microRNA, circular RNA, lncRNA and various compounds have been developed to target YB-1 for cancer therapy. In this review, we describe the physiological characteristics of YB-1 in detail, highlight the role of YB-1 in tumors and summarize the current therapeutic methods for targeting YB-1 in cancer.
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