反硫化
半胱氨酸
生物
胱氨酸
半胱氨酸代谢
胱硫醚β合酶
生物化学
癌症
新陈代谢
氨基酸
遗传学
酶
作者
Haifeng Zhang,Ramon I. Klein Geltink,Seth J. Parker,Poul H. Sorensen
标识
DOI:10.1016/j.tcb.2022.02.009
摘要
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.
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