| Literature DB >> 35365367 |
Hai-Feng Zhang1, Ramon I Klein Geltink2, Seth J Parker3, Poul H Sorensen4.
Abstract
Cysteine, a thiol-containing amino acid, is crucial for the synthesis of sulfur-containing biomolecules that control multiple essential cellular activities. Altered cysteine metabolism has been linked to numerous driver oncoproteins and tumor suppressors, as well as to malignant traits in cancer. Cysteine can be acquired from extracellular sources or synthesized de novo via the transsulfuration (TSS) pathway. Limited availability of cystine in tumor interstitial fluids raises the possible dependency on de novo cysteine synthesis via TSS. However, the contribution of TSS to cancer metabolism remains highly contentious. Based on recent findings, we provide new perspectives on this crucial but understudied metabolic pathway in cancer.Entities:
Keywords: cancer; cysteine metabolism; ferroptosis; glutathione; redox homeostasis; transsulfuration
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Year: 2022 PMID: 35365367 PMCID: PMC9378356 DOI: 10.1016/j.tcb.2022.02.009
Source DB: PubMed Journal: Trends Cell Biol ISSN: 0962-8924 Impact factor: 21.167