The iron chelator deferriferrichrysin induces paraptosis via extracellular signal-related kinase activation in cancer cells

Cancer cells generally exhibit increased iron uptake, which contributes to their abnormal growth and metastatic ability. Iron Chelators have thus recently attracted attention as potential Anticancer agents. Here, we show that deferriferrichrysin (Dfcy), a natural product from Aspergillus oryzae acts as an iron chelator to induce Paraptosis (a programmed cell death pathway characterized by ER dilation) in MCF-7 human breast Cancer cells and H1299 human lung Cancer cells. We first examined the Anticancer efficacy of Dfcy in Cancer cells and found that Dfcy induced ER dilation and reduced the number of viable cells. Extracellular signal-related kinase (ERK) was activated by Dfcy treatment, and the MEK Inhibitor U0126, a small molecule commonly used to inhibit ERK activity, prevented the increase in ER dilation in Dfcy-treated cells. Concomitantly, the decrease in the number of viable cells upon treatment with Dfcy was attenuated by U0126. Taken together, these results demonstrate that the iron chelator Dfcy exhibits Anticancer effects via induction of ERK-dependent Paraptosis.

anticancer; cell death; cytoplasmic vacuolization; endoplasmic reticulum; iron chelator; paraptosis.