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Current Cancer Drug Targets

Editor-in-Chief

ISSN (Print): 1568-0096
ISSN (Online): 1873-5576

Mini-Review Article

Potential Therapeutic Strategies for Targeting Y-Box-Binding Protein 1 in Cancers

Author(s): Jia-Wei Yang, Chao Sun, Qiu-Yang Jin, Xing-Hui Qiao and Xiu-Li Guo*

Volume 21, Issue 11, 2021

Published on: 31 August, 2021

Page: [897 - 906] Pages: 10

DOI: 10.2174/1568009621666210831125001

Price: $65

Abstract

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.

Keywords: Y-box-binding protein 1, cancer, nuclear translocation model, siRNA, shRNA, microRNA, circular RNA, lncRNA.

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