Single-cell encoded gene silencing for high-throughput combinatorial siRNA screening

被引:0
|
作者
Guo, Feng [1 ,2 ]
Ji, Xianglin [1 ]
Xiong, Chuxiao [1 ]
Sun, Hailiang [1 ]
Liang, Zhenghua [3 ]
Yan-Do, Richard [1 ,2 ]
Gai, Baowen [4 ]
Gao, Feng [4 ]
Huang, Linfeng [5 ,6 ]
Li, Zhongping [7 ]
Kuang, Becki Yi [3 ]
Shi, Peng [1 ,2 ,8 ,9 ]
机构
[1] City Univ Hong Kong, Dept Biomed Engn, Kowloon, Hong Kong 999077, Peoples R China
[2] Hong Kong Sci Pk, Hong Kong Ctr Cerebrocardiovasc Hlth Engn, Hong Kong 999077, Peoples R China
[3] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Kowloon, Hong Kong 999077, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Colorectal Surg, Dept Gen Surg, Guangzhou 510655, Peoples R China
[5] Duke Kunshan Univ, Div Nat & Appl Sci, Wang Cai Biochem Lab, Kunshan, Jiangsu, Peoples R China
[6] Duke Kunshan Univ, Global Hlth Res Ctr, Kunshan, Jiangsu, Peoples R China
[7] Shanxi Univ, Inst Environm Sci, Taiyuan 030006, Peoples R China
[8] City Univ Hong Kong, Ctr Superdiamond & Adv Films COSDAF, Kowloon, Hong Kong 999077, Peoples R China
[9] City Univ Hong Kong, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA; INTERFERENCE; POTENT;
D O I
10.1038/s41467-024-53419-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The use of combinatorial siRNAs shows great promise for drug discovery, but the identification of safe and effective siRNA combinations remains challenging. Here, we develop a massively multiplexed technology for systematic screening of siRNA-based cocktail therapeutics. We employ composite micro-carriers that are responsive to near infrared light and magnetic field to achieve photoporation-facilitated siRNA transfection to individual cells. Thus, randomized gene silencing by different siRNA formulations can be performed with high-throughput single-cell-based analyses. For screening anti-cancer siRNA cocktails, we test more than 1300 siRNA combinations for knocking down multiple genes related to tumor growth, discovering effective 3-siRNA formulations with an emphasis on the critical role of inhibiting Cyclin D1 and survivin, along with their complementary targets for synergic efficacy. This approach enables orders of magnitude reduction in time and cost associated with largescale siRNA screening, and resolves key insights to siRNA pharmacology that are not permissive to existing methods. Combined use of multiple siRNAs promises a new path for drug development. Here, the authors demonstrate a multiplexed combinatorial screening of thousands of siRNA formulations through highthroughput single-cell gene silencing, discovering the most effective anti-cancer siRNA cocktail therapeutics.
引用
收藏
页数:15
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