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The analysis of mutational signatures in patients suggests that the selection of mutation-dependent oncogenic signals might trigger distinct phenotypes in permissive tissues (Haigis et al, 2019

doi: 10.1016/j.cofs.2021.11.006 126 National Bureau of Statistics of China

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5.4 Ferroptosis in retinitis pigmentosa RP refers to a group of inherited retinal diseases whose main feature is the slow degradation of PR cells, leading to a gradual decline in the patients vision

4.3.1 Melatonin inhibiting glycolysis in T-cell malignancy Glycolysis is a metabolic mechanism that transforms glucose into pyruvate and generates ATP, the primary source of energy for cells

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