| Literature DB >> 31303578 |
Elena S Reckzeh1, George Karageorgis2, Melanie Schwalfenberg2, Javier Ceballos2, Jessica Nowacki2, Marcus C M Stroet2, Aylin Binici2, Lena Knauer3, Silke Brand2, Axel Choidas4, Carsten Strohmann3, Slava Ziegler2, Herbert Waldmann5.
Abstract
Cancer cells sustain growth by altering their metabolism to accelerated aerobic glycolysis accompanied by increased glucose demand and employ glutamine as additional nutrient source. This metabolic adaptation induces upregulation of glucose transporters GLUT-1 and -3, and simultaneous targeting of both transporters and of glutamine metabolism may offer a promising approach to inhibit cancer cell growth. We describe the discovery of the very potent glucose uptake inhibitor Glutor, which targets glucose transporters GLUT-1, -2, and -3, attenuates glycolytic flux and potently and selectively suppresses growth of a variety of cancer cell lines. Co-treatment of colon cancer cells with Glutor and glutaminase inhibitor CB-839 very potently and synergistically inhibits cancer cell growth. Such a dual inhibition promises to be particularly effective because it targets the metabolic plasticity as well as metabolic rescue mechanisms in cancer cells.Entities:
Keywords: GLUT-1; GLUT-3; Warburg effect; co-treatment; glutaminase; metabolic plasticity; small molecule
Year: 2019 PMID: 31303578 DOI: 10.1016/j.chembiol.2019.06.005
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116