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Consequently, this heightened metabolic rate not only underscores the aggressive nature of the disease but also offers potential therapeutic targets for disrupting tumor growth ( The significant abundance of SLC7A11 suggests its potential as a promising target for tumor therapy ( + T cells, which release IFN- to enhance tumor cell ferroptosis via PD-L1 inhibition ( Given the pivotal role of SLC7A11 in cancer treatment, this paper provides an overview of its structure and biological functions, as well as its involvement in oxidative stress, tumor metabolism, immune modulation, and cell death ( Figure 1 )

Type 1 Collagen: Synthesis, Structure and Key Functions in Bone Mineralization

Such an understanding could facilitate the development of targeted interventions to mitigate the effects of age-related epigenetic changes on liver health

Similarly, in lipopolysaccharide (LPS)-induced cardiomyocytes, METTL3 deficiency inhibited LPS-induced ferroptosis by upregulating the expression of SLC7A11 in an m 6 A methylation-dependent manner[160]