Knockdown of Long Non-coding RNA SNGH3 by CRISPR-dCas9 Inhibits the Progression of Bladder Cancer

被引:6
作者
Cao, Yu [1 ]
Hu, Qiong [1 ]
Zhang, Ruiming [1 ]
Li, Ling [2 ]
Guo, Mingjuan [3 ]
Wei, Huiling [3 ]
Zhang, Li [3 ]
Wang, Jianfeng [3 ]
Li, Chunjing [3 ]
机构
[1] Hunan Univ Tradit Chinese Med, Ningxiang Hosp, Ningxiang, Peoples R China
[2] Hunan Univ Chinese Med, Coll Tradit Chinese Med, Med Basic Teaching Expt Ctr, Changsha, Peoples R China
[3] Southern Med Univ, Affiliated Foshan Maternal & Child Healthcare Hos, Dept Urol, Foshan, Peoples R China
基金
湖南省自然科学基金;
关键词
SNGH3; bladder cancer; CRISPR-dCas9; lncRNA; therapeutic target; METASTASIS;
D O I
10.3389/fmolb.2021.657145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent research evidence documents that lncRNAs (long non-coding RNAs lncRNAs) play a pivotal role in the tumorigenesis and development of tumors. LncRNA SNGH3 (small nucleolar RNA host gene 3) is highly expressed in numerous forms of cancer, serving as an oncogene in cancer progression. Nonetheless, the clinical relationship, along with the mechanism of SNGH3 in bladder cancer, have not been studied. Herein, the findings exhibited upregulation of SNGH3 in bladder cancer tissues, along with the cell lines. Furthermore, overexpressed SNGH3 was positively linked to the TNM stage, as well as the histological grade of bladder cancer. Moreover, the silencing of SNGH3, using CRISPR-dCas9, suppressed cell growth along with migration, but elevated bladder cancer cell apoptosis. In summary, we established that SNGH3 serves as a bladder cancer oncogene and could be employed as a prospective diagnostic marker for clinical use, and is also a therapeutic target for CRISPR-mediated gene therapy.
引用
收藏
页数:9
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