RT Journal Article
SR Electronic
T1 Accelerated lipid catabolism and autophagy are cancer survival mechanisms under inhibited glutaminolysis
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 230433
DO 10.1101/230433
A1 Anna Halama
A1 Michal Kulinski
A1 Shaima S. Dib
A1 Shaza B. Zaghlool
A1 Kodappully S. Siveen
A1 Ahmad Iskandarani
A1 Noothan J. Satheesh
A1 Aditya M. Bhagwat
A1 Shahab Uddin
A1 Gabi Kastenmüeller
A1 Olivier Elemento
A1 Steven S. Gross
A1 Karsten Suhre
YR 2018
UL http://biorxiv.org/content/early/2018/01/15/230433.abstract
AB Suppressing glutaminolysis does not always induce cancer cell death in glutamine-dependent tumors because cells may switch to alternative energy sources. To reveal compensatory metabolic pathways, we investigated the metabolome-wide cellular response to inhibited glutaminolysis. We conducted metabolic profiling in the triple-negative breast cancer cell line MB-MDA-231, treated with different dosages of glutaminase inhibitor C.968 at multiple time points. We found that multiple molecules involved in lipid catabolism responded directly to glutamate deficiency as a presumed compensation for energy deficit. Accelerated lipid catabolism, together with oxidative stress induced by glutaminolysis inhibition, triggered autophagy. We therefore simultaneously inhibited glutaminolysis and autophagy, which induced cancer cell death. Our study emphasizes the potential of non-targeted metabolomics to characterize and identify metabolic escape mechanisms contributing to cancer cell survival under treatment. Our findings add to the increasing evidence that combined inhibition of glutaminolysis and autophagy may be effective in glutamine-addicted cancers.