Cystine ferroptosis
WebApr 7, 2024 · Ferroptosis is an iron-dependent type of "programmed cell death" or a biological process that causes cells to "self-destruct" on command. Our bodies don't … WebFerroptosis can be induced chemically by erastin, which inhibits the glutamate/cystine antiporter, and subsequently suppresses cellular cystine uptake and depletes glutathione. Glutathione is fundamental in maintaining the redox balance and defending against oxidative stress, including reactive oxygen species (Kim et al., 2015).
Cystine ferroptosis
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WebOct 14, 2024 · A recent study from Nature Communications reveals that Mycobacterium tuberculosis can hijack epigenetic machinery in host cells and induce host cell ferroptosis, which promotes pathogen... WebJun 15, 2024 · The cystine transporter SLC7A11 was identified as a druggable target downstream of the MCU-Nrf2 axis. Paradoxically, despite the increased ability to uptake cystine, MCU-overexpressing PDAC demonstrated characteristics typical of cystine-deprived cells and were hypersensitive to cystine deprivation-induced ferroptosis.
WebApr 12, 2024 · Ferroptosis is an iron-dependent antioxidant system imbalance, ... (SLC3A2) constitute system Xc- together on the cell membrane, which exports glutamate and imports cystine at a 1:1 ratio. Cystine is rapidly transformed into cysteine intracellularly, the rate-limiting amino acid for the synthesis of GSH. WebFeb 23, 2024 · Accumulation of lipid peroxides leads to ferroptosis. In cells with high SLC7A11 levels and cystine import, GPX4 reduces lipid peroxidation and ferroptosis at …
WebApr 3, 2024 · In addition, cystine is the most restricted amino acid in the process of GSH synthesis, so the cystine-importing GSH-GPX4 machinery is the most critical signaling pathway for preventing ferroptosis. It has been reported that the cystine/glutamate antiporter system Xc - can promote ferroptosis by inhibiting cysteine import. WebAug 9, 2024 · Within the cyst (e)ine/GSH/GPX4 axis, cysteine is the rate-limiting metabolite for GSH biosynthesis, hence the ferroptosis-inducing activity of cyst (e)ine depletion …
WebFerroptosis is a new mode of cell death discovered in recent years, which emerged after the discovery that a small molecule compound, erastin and RSL-3, could induce a unique form of cell death in cells. 1, 2 In 2012, this method of death was officially named “Ferroptosis” by Dixon. 3 The research in the past decade has exponentially due to ...
WebOct 14, 2024 · Once imported into the cytosol, cystine is reduced to cysteine for subsequent synthesis of glutathione (GSH), which is then used as a key cofactor by glutathione peroxidase 4 (GPX4) to detoxify lipid peroxides accumulated on cellular membranes, thereby mitigating ferroptosis ( Fig. 1A) ( Yang et al., 2014 ). ease of travel restrictionsWebOct 2, 2024 · Ferroptosis, another form of cell death, has been observed many times. Cell death caused by insufficient cystine was discovered in the 1950s, and it could be rescued by the lipophilic antioxidant, tocopherol, a component of vitamin E [ 3, 4 ]. ease of use access centerWebAug 15, 2024 · DOI: 10.1016/j.aca.2024.05.049 Corpus ID: 220606876; In vivo tracking cystine/glutamate antiporter-mediated cysteine/cystine pool under ferroptosis. … ease of use and usabilityWebCystine transporter SLC7A11/xCT in cancer: ferroptosis, nutrient dependency, and cancer therapy The cystine/glutamate antiporter SLC7A11 (also commonly known as xCT) functions to import cystine for glutathione biosynthesis and antioxidant defense and is … ease of use google sheets external apisWebApr 11, 2024 · Ferroptosis was initially described as a form of cell death that is induced by erastin and RSL3 through the inhibition of cystine uptake via system x c − and GPX4, respectively . Given that cystine is an essential component of GSH, which is a co-factor of GPX4, the system x c − -GSH-GPX4 pathway was first established as the core defense ... ease of use settings displayWebOct 1, 2024 · It is reported that cystine transporter SLC7A11 is upregulated in lung cancer stem-like cells (CSLC) and can be activated by stem cell transcriptional factor SOX2 and suggests that oxidation of SOX1 can be a potential therapeutic target for cancer treatment. 39 PDF View 1 excerpt, cites background ct to key westease of use and usefulness