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Therapeutic Methods and Therapies TCIM
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1.
J Biol Chem ; 299(4): 103039, 2023 04.
Article in English | MEDLINE | ID: mdl-36803962

ABSTRACT

The small molecule erastin inhibits the cystine-glutamate antiporter, system xc-, which leads to intracellular cysteine and glutathione depletion. This can cause ferroptosis, which is an oxidative cell death process characterized by uncontrolled lipid peroxidation. Erastin and other ferroptosis inducers have been shown to affect metabolism but the metabolic effects of these drugs have not been systematically studied. To this end, we investigated how erastin impacts global metabolism in cultured cells and compared this metabolic profile to that caused by the ferroptosis inducer RAS-selective lethal 3 or in vivo cysteine deprivation. Common among the metabolic profiles were alterations in nucleotide and central carbon metabolism. Supplementing nucleosides to cysteine-deprived cells rescued cell proliferation in certain contexts, showing that these alterations to nucleotide metabolism can affect cellular fitness. While inhibition of the glutathione peroxidase GPX4 caused a similar metabolic profile as cysteine deprivation, nucleoside treatment did not rescue cell viability or proliferation under RAS-selective lethal 3 treatment, suggesting that these metabolic changes have varying importance in different scenarios of ferroptosis. Together, our study shows how global metabolism is affected during ferroptosis and points to nucleotide metabolism as an important target of cysteine deprivation.


Subject(s)
Cysteine , Ferroptosis , Nucleotides , Piperazines , Cell Death , Cysteine/metabolism , Glutathione Peroxidase/metabolism , Lipid Peroxidation , Piperazines/pharmacology , Nucleotides/metabolism
2.
Mol Cell ; 78(6): 1034-1044, 2020 06 18.
Article in English | MEDLINE | ID: mdl-32504556

ABSTRACT

Malignant cells remodel their metabolism to meet the demands of uncontrolled cell proliferation. These demands lead to differential requirements in energy, biosynthetic precursors, and signaling intermediates. Both genetic programs arising from oncogenic events and transcriptional programs and epigenomic events are important in providing the necessary metabolic network activity. Accumulating evidence has established that environmental factors play a major role in shaping cancer cell metabolism. For metabolism, diet and nutrition are the major environmental aspects and have emerged as key components in determining cancer cell metabolism. In this review, we discuss these emerging concepts in cancer metabolism and how diet and nutrition influence cancer cell metabolism.


Subject(s)
Diet Therapy/methods , Neoplasms/diet therapy , Neoplasms/metabolism , Carcinogenesis/metabolism , Cell Proliferation/genetics , Diet/trends , Diet Therapy/trends , Energy Metabolism/genetics , Humans , Metabolic Networks and Pathways/genetics , Metabolic Networks and Pathways/physiology , Neoplasms/genetics , Nutrition Therapy/methods , Signal Transduction/genetics
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