A living cell-based fluorescent reporter for high-throughput screening of anti-tumor drugs

被引:0
|
作者
Tang, Ningning [1 ,2 ]
Li, Ling [1 ,2 ]
Xie, Fei [1 ,2 ]
Lu, Ying [1 ,2 ]
Zuo, Zifan [1 ,2 ]
Shan, Hao [3 ]
Zhang, Quan [1 ,2 ]
Zhang, Lianwen [1 ,2 ]
机构
[1] Nankai Univ, Coll Pharm, Tianjin 300350, Peoples R China
[2] Nankai Univ, Tianjin Key Lab Mol Drug Res, Tianjin 300350, Peoples R China
[3] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent reporter; High-throughput screening; O-linked β -N-acetylglucosaminylation; Anti-tumor drug; Gene transcriptional regulation; O-GLCNAC TRANSFERASE; N-ACETYLGLUCOSAMINE; CANCER CELLS; CHEMICAL TOOLS; BETA-CATENIN; GLCNACYLATION; SESAMIN; METASTASIS; MODULATION; MECHANISMS;
D O I
10.1016/j.jpha.2021.04.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Suppression of cellular O-linked 13-N-acetylglucosaminylation (O-GlcNAcylation) can repress proliferation and migration of various cancer cells, which opens a new avenue for cancer therapy. Based on the regulation of insulin gene transcription, we designed a cell-based fluorescent reporter capable of sensing cellular O-GlcNAcylation in HEK293T cells. The fluorescent reporter mainly consists of a reporter (green fluorescent protein (GFP)), an internal reference (red fluorescent protein), and an operator (neuronal differentiation 1), which serves as a "sweet switch" to control GFP expression in response to cellular OGlcNAcylation changes. The fluorescent reporter can efficiently sense reduced levels of cellular OGlcNAcylation in several cell lines. Using the fluorescent reporter, we screened 120 natural products and obtained one compound, sesamin, which could markedly inhibit protein O-GlcNAcylation in HeLa and human colorectal carcinoma-116 cells and repress their migration in vitro. Altogether, the present study demonstrated the development of a novel strategy for anti-tumor drug screening, as well as for conducting gene transcription studies. (c) 2021 Xi'an Jiaotong University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:808 / 814
页数:7
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