Xing Fuqiang, Ai Nana, Huang Shigao, Jiang Cheng, Mughal Muhammad Jameel, Ge Wei, Wang Guanyu, Deng Chu-Xia
Cancer Center, Faculty of Health Sciences, University of Macau, Macau SAR, China.
Department of Biology, School of Life Sciences, Guangdong Provincial Key Laboratory of Computational Science and Material Design, Southern University of Science and Technology, Shenzhen, China.
Front Bioeng Biotechnol. 2022 Feb 14;10:839078. doi: 10.3389/fbioe.2022.839078. eCollection 2022.
In the present study, an efficient drug screening platform is established based on FRET technique. We transfected cancer cells with FRET-based caspase-3 (C3) sensor and validated the cell lines by detecting the change in FRET signal caused by the drug-induced cell apoptosis. Furthermore, the C3 expressing cancer cells were then injected into zebrafish embryos and nude mice to establish the corresponding xenograft models. We found that cancer cell lines expressing C3 were effective in detecting cell death following drug treatment, including the detection of the tipping point of apoptosis. The drug-induced cell apoptosis was also observed in both zebrafish embryos and nude mice xenograft models. Overall, the FRET-based platform, through imaging, is potentially useful to improve drug screening efficiency.
在本研究中,基于荧光共振能量转移(FRET)技术建立了一个高效的药物筛选平台。我们用基于FRET的半胱天冬酶-3(C3)传感器转染癌细胞,并通过检测药物诱导的细胞凋亡引起的FRET信号变化来验证细胞系。此外,将表达C3的癌细胞注射到斑马鱼胚胎和裸鼠体内,建立相应的异种移植模型。我们发现,表达C3的癌细胞系在检测药物治疗后的细胞死亡方面有效,包括检测细胞凋亡的临界点。在斑马鱼胚胎和裸鼠异种移植模型中也观察到了药物诱导的细胞凋亡。总体而言,基于FRET的平台通过成像,可能有助于提高药物筛选效率。