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These studies indicate that VacA may contribute to the ferroptosis in GC progression by increasing ROS levels and disrupting the metabolism of GSH through various mechanisms, but there is no reports on the morphology and related proteins of ferroptosis cells with VacA, which is worthy of further investigation

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Earlier work had shown that the -amino groups of lysine residues are susceptible to thioacylation (Fisher et al., 1993, Harris et al., 1992, Hayden and Stevens, 1990, Hayden et al., 1991)

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Our study had several limitations