结直肠癌
癌症研究
癌基因
基因敲除
细胞周期
下调和上调
生物
癌症干细胞
癌症
细胞生长
诱导多能干细胞
细胞凋亡
胚胎干细胞
基因
遗传学
作者
Lixiong Luo,Yijiang Li,Rongjie Huang,Ling Li,Chuncai Wu,Qunzhang Zeng
出处
期刊:Neoplasma
[AEPress]
日期:2024-01-01
卷期号:71 (01): 13-21
标识
DOI:10.4149/neo_2023_230629n339
摘要
Cancer stem cells (CSCs) have emerged as crucial contributors to tumor relapse and chemoresistance, making them promising targets for treating cancers like colorectal cancer (CRC).However, the mechanisms governing CSC maintenance in CRC remain poorly characterized.In this study, we investigated the potential role of ubiquitin-specific protease 36 (USP36) in CRC.Our bioinformatic analysis revealed a significant upregulation of USP36 expression in CRC, and high USP36 levels were associated with poor prognosis in CRC patients.Furthermore, we observed an increase in USP36 expression in CRC cell lines.Knockdown of USP36 resulted in reduced viability, cell cycle arrest, increased apoptosis, and impaired migration and invasion in CRC cells.Additionally, the colony formation and sphere formation ability, as well as the expression of stem cell markers and pluripotent transcription factors, were substantially reduced in USP36-deficient CRC cells.These findings emphasize the role of USP36 as an oncogene in CRC, highlighting its potential as a therapeutic target for the treatment of CRC.
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