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Yoshida et al., 2013), OAS C as a target of GRX (Rouhier et al., 2005), while OAS A1, OAS B, and OAS C have been reported as being persulfidated (Figure 2 and Supplementary Table 2

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They voluntarily agreed to participate with full knowledge and understanding of the aims and scope of the study

The aberrant activation of ALOX5 is important for the proliferation and migration of breast cancer cells [21], whereas the absence of ALOX5 promotes the progression of bladder cancer by enabling the evasion of ferroptosis [22]

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