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Inhibition of bacterial decarboxylation pathways could therefore represent a strategy to increase levodopa absorption

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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 )