Targeting ITGB4/SOX2-driven lung cancer stem cells using proteasome inhibitors

利用蛋白酶体抑制剂靶向ITGB4/SOX2驱动的肺癌干细胞

阅读:2
作者:Linlin Guo ,Atish Mohanty ,Sharad Singhal ,Saumya Srivastava ,Arin Nam ,Charles Warden ,Sravani Ramisetty ,Yate-Ching Yuan ,Hyejin Cho ,Xiwei Wu ,Aimin Li ,Manik Vohra ,Srinivas Vinod Saladi ,Deric Wheeler ,Leonidas Arvanitis ,Erminia Massarelli ,Prakash Kulkarni ,Yiming Zeng ,Ravi Salgia

Abstract

This study investigates the role of integrin β4 (ITGB4) and stemness-associated factor SOX2 in platinum resistance in lung squamous cell carcinoma (LUSC). The expression of SOX2 and ITGB4 is found to be high in all LUSC subtypes, but the impact of ITGB4 expression on overall patient survival varies by subtype. Cancer stem cells (CSCs) isolated from LUSC patients were found to be resistant to cisplatin, but knocking down ITGB4 or SOX2 sensitized them to cisplatin. Carfilzomib (CFZ) synergized with cisplatin and suppressed CSC growth by inhibiting ITGB4 and SOX2 expression. Additionally, CFZ was found to inhibit SOX2 expression epigenetically by inhibiting histone acetylation at the SOX2 promoter site. CFZ also suppressed the growth of SOX2-dependent small cell lung cancer cells in vitro and in vivo. The study highlights the unique function of CFZ as a transcriptional suppressor of SOX2, independent of its proteasome inhibitory function.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。