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observed similar ultrastructural changes in the rats kidney after MTX treatment, and they attributed these alterations to the direct toxic effects of MTX metabolites that affect membrane permeability

Meanwhile, the activity of the cysteine-glutamate transporter protein system XC- activity is inhibited, further exacerbating the process

In addition to an increase in inflammation levels, the number of tumor cells also increased in the number of tumor cells after GPX3 KO during the development of colitis-related cancers ( As mentioned earlier, the vast majority of GPX3 is secreted by the renal proximal convoluted tubules, so we speculate that the kidney may be a highly expressed organ of GPX3, and to test our hypothesis, we analyzed the GSE111159 dataset (This dataset mainly detects the gene sequencing of 10 tissues and organs of mouse kidney, liver, brain, lung, thymus, muscle, spleen, stomach, heart and testicle under physiological conditions to understand the gene expression of each tissue and organ) in the GEO database (Gene Expression Omnibus, We found that GPX3 had the highest level of expression in kidney tissue under mouse physiology (Figure 3A), which is consistent with the results of the analysis by Kim et al