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. 2022 Jun 2;13(6):521. doi: 10.1038/s41419-022-04974-8

Fig. 3. Ferritinophagy mediates ferroptotic tumor suppression.

Fig. 3

A Western blot analysis of protein expression in control and ATG5-knockdown Y79-CR cells following treatment with erastin (10 µM) for 24 h. B Analysis of intracellular free iron in control and ATG5-knockdown Y79-CR cells following treatment with erastin (10 µM) for 8–24 h (two-way ANOVA with Tukey’s multiple comparisons test; data are presented as mean ± SD; n = 3 biologically independent samples). C Western blot analysis of protein expression in control and NCOA4-knockdown Y79-CR cells following treatment with erastin (10 µM) for 24 h. D Analysis of intracellular free iron in control and NCOA4-knockdown Y79-CR cells following treatment with erastin (10 µM) for 8–24 h (two-way ANOVA with Tukey’s multiple comparisons test; data are presented as mean ± SD; n = 3 biologically independent samples). EH Indicated Y79-CR cells were treated with erastin (5–10 µM) for 24 h, and then cell viability (E), cell death (F), HMGB1 release (G), and lipid ROS (H) were assayed (two-way ANOVA with Tukey’s multiple comparisons test; data are presented as mean ± SD; n = 3 biologically independent samples).