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. 2021 May 15;11(5):1895–1912.

Figure 1.

Figure 1

The schematic diagram of some iron-related pathway in cancer cells. The excess iron would impact the degradation of p53, then promote the tumorigenicity; iron binds the protein CDK1 activate 4E-BP1, then lead to translation of GP130 via JAK/STAT3 pathway; Fe2+ produce ROS in cancer cells which inhibits the proliferation of cells trough p53/p21/p38 MAPK pathway; p53 could also inhibit the uptake of cystine to repress expression of SLC7A11, and then promote the ferroptosis in cancer cells.