1. Academic Validation
  2. Drug Screening for Glycolysis Pathway in Living Cancer Cells Using 19F NMR

Drug Screening for Glycolysis Pathway in Living Cancer Cells Using 19F NMR

  • Anal Chem. 2025 May 6;97(17):9192-9201. doi: 10.1021/acs.analchem.4c06149.
Biao Liu 1 Tao Huang 1 Xiong Xiao 1 2 Xin Chai 1 Yating Lei 1 2 Qiuyun Sun 1 Qin Hu 1 2 Qinjun Zhu 1 Danyun Zeng 1 2 Caixiang Liu 1 2 Lichun He 1 2 Zhou Gong 1 2 Bin Jiang 1 2 3 Xin Zhou 1 2 3 Maili Liu 1 2 3 Xu Zhang 1 2 3
Affiliations

Affiliations

  • 1 Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, State Key Laboratory of Magnetic Resonance Spectroscopy and Imaging, National Center for Magnetic Resonance in Wuhan, Wuhan Institute of Physics and Mathematics, Innovation Academy for Precision Measurement of Science and Technology, Chinese Academy of Sciences, Wuhan 430071, China.
  • 2 University of Chinese Academy of Sciences, Beijing 100049, China.
  • 3 Optics Valley Laboratory, Wuhan 430074, China.
Abstract

Glycolysis is a fundamental process for the generation of cellular energy, and its dysregulation has been linked to a number of diseases, including obesity, neurological disorders, and Cancer. Targeting glycolysis is therefore a promising therapeutic strategy. However, effective drugs that specifically target glycolysis are still lacking. In this study, we introduce a novel approach utilizing 19F NMR to monitor early glycolysis in living MCF-7 cells. By tracking metabolites downstream of the glucose analogue 2-fluoro-2-deoxyglucose (2-FDG), we successfully observed the activity of key glycolytic components, such as glucose transporters (GLUTs) and Hexokinase (HKs). Our results reveal distinct metabolic profiles upon inhibition of these targets, advancing the understanding of glycolytic regulation. In addition, we applied this approach to screen traditional Chinese medicines for their effects on glycolysis and identified Salvia miltiorrhiza and Fructus evodiae as modulators with contrasting effects on glycolytic metabolism. This dual modulation highlights their potential as valuable tools for therapeutic intervention. Our study provides an innovative methodology for both the exploration of glycolytic pathways and the discovery of novel therapeutics, offering new perspectives for drug development targeting metabolic diseases.

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