Ubiquitin specific peptidase 5 regulates colorectal cancer cell growth by stabilizing Tu translation elongation factor

基因敲除 脱氮酶 细胞生长 癌症研究 生物 泛素 癌变 细胞生物学 细胞培养 化学 癌症 基因 遗传学
作者
Xin Xu,Aiwen Huang,Ximao Cui,Kunkun Han,Xiaodan Hou,Qun Wang,Long Cui,Yili Yang
出处
期刊:Theranostics [Ivyspring International Publisher]
卷期号:9 (14): 4208-4220 被引量:61
标识
DOI:10.7150/thno.33803
摘要

Ubiquitin specific peptidase 5 (USP5) is a ubiquitous expressed deubiquitinating enzyme (DUB).It has been shown involved in DNA repair, apoptosis, inflammation, and tumor cell growth.However, the function and molecular mechanism of USP5 in colorectal cancer (CRC) are still unclear.In the present study, we asked how it affected the growth of colorectal cancer cells.Methods: A shRNA-based high-content screening was performed to identify DUBs affecting the growth of CRC cells.CCK-8 assay and xenografts were used to assess CRC cell growth, survival and tumorigenesis.RT-qPCR, immunoblotting and immunohistochemistry were carried out to quantitate USP5 expression in CRC tissues and cell lines.Immunoprecipitation and mass spectrometry analysis were performed to identify USP5-interacting proteins.Cycloheximide chase was performed to assess Tu translation elongation factor (TUFM) stability.Dual luciferase reporter assay was utilized for USP5 promoter analysis.Results: We found that USP5 was highly expressed in a group of primary CRC tissues, and the increased USP5 was correlated with clinical stages and shorter overall survival.While USP5 knockdown effectively inhibited CRC cell growth, overexpressed USP5 promoted the growth of CRC cells and made them more resistant to doxorubicin (DOX).TUFM was discovered as a substrate of USP5.USP5 deubiquitinated TUFM and increased its level in CRC cells.Enforced expression of TUFM was able to alleviate the growth inhibition induced by USP5 knockdown.Further analyses showed that EBF transcription factor 1 (EBF1) was a major regulator for USP5 transcription, and DOX inhibited EBF1-USP5-TUFM axis in CRC cells.Conclusions: USP5 was required for CRC cells and promoted their growth and resistance to chemotherapeutics.TUFM was a USP5 deubiquitinating substrate that mediated the cellular effects of USP5.The transcription of USP5 was regulated by EBF1.Thus, targeting EBF1-USP5-TUFM axis is a potential novel strategy for CRC treatment.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
优雅的平安完成签到 ,获得积分10
1秒前
poki完成签到 ,获得积分10
9秒前
dizi完成签到 ,获得积分10
9秒前
学术小子完成签到 ,获得积分10
14秒前
LYZ完成签到,获得积分10
17秒前
17秒前
无限的千凝完成签到 ,获得积分10
22秒前
26秒前
赵李锋完成签到,获得积分10
34秒前
Lucas应助你是我的唯一采纳,获得10
37秒前
黑布林大李子完成签到,获得积分0
46秒前
46秒前
51秒前
所所应助搞怪的凤灵采纳,获得50
58秒前
Lucas应助搞怪的凤灵采纳,获得50
58秒前
58秒前
科研通AI2S应助搞怪的凤灵采纳,获得30
58秒前
完美世界应助搞怪的凤灵采纳,获得30
58秒前
星辰大海应助搞怪的凤灵采纳,获得30
58秒前
在水一方应助搞怪的凤灵采纳,获得10
58秒前
余味应助搞怪的凤灵采纳,获得10
58秒前
慕青应助搞怪的凤灵采纳,获得10
58秒前
1分钟前
yk完成签到,获得积分10
1分钟前
Vivian完成签到 ,获得积分10
1分钟前
1分钟前
Lea发布了新的文献求助10
1分钟前
Youlu发布了新的文献求助10
1分钟前
土豆晴完成签到 ,获得积分10
1分钟前
思源应助Lea采纳,获得10
1分钟前
1分钟前
1分钟前
小二郎应助Youlu采纳,获得10
1分钟前
linhuafeng完成签到 ,获得积分10
1分钟前
你是我的唯一完成签到,获得积分10
1分钟前
1分钟前
爱撒娇的孤丹完成签到 ,获得积分10
1分钟前
mqbucm完成签到,获得积分10
1分钟前
温暖的颜演完成签到 ,获得积分10
1分钟前
豆泡终结者完成签到 ,获得积分10
1分钟前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Technologies supporting mass customization of apparel: A pilot project 450
Mixing the elements of mass customisation 360
Периодизация спортивной тренировки. Общая теория и её практическое применение 310
the MD Anderson Surgical Oncology Manual, Seventh Edition 300
Nucleophilic substitution in azasydnone-modified dinitroanisoles 300
Political Ideologies Their Origins and Impact 13th Edition 260
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3780879
求助须知:如何正确求助?哪些是违规求助? 3326359
关于积分的说明 10226694
捐赠科研通 3041539
什么是DOI,文献DOI怎么找? 1669502
邀请新用户注册赠送积分活动 799081
科研通“疑难数据库(出版商)”最低求助积分说明 758732