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BECN1 is a new driver of ferroptosis

Open access
Kang, Rui, Zhu, Shan, Zeh, Herbert J., Klionsky, Daniel J., Tang, Daolin·2018·Autophagy

Abstract

Ferroptosis is a form of regulated cell death caused by iron accumulation and oxidative injury. BECN1 is a key regulator of macroautophagy/autophagy, a catabolic process of degradation induced by starvation or other stressors. Our recent findings reveal a novel alternative mechanism by which BECN1 can promote ferroptosis through the regulation of activity of the cysteine and glutamate antiporter system xc− in cancer cells. BECN1-dependent autophagy requires the formation of the BECN1-containing class III phosphatidylinositol 3-kinase (PtdIns3K) complex, whereas BECN1-dependent ferroptosis requires the formation of a BECN1-SLC7A11 complex. Furthermore, AMP-activated protein kinase (AMPK) is required for BECN1 phosphorylation to trigger formation of the BECN1-SLC7A11 complex in the process of inhibiting system xc− activity and inducing lipid peroxidation. These findings suggest that the autophagy-dependent and -independent functions of BECN1 play distinct roles in regulated cell death.

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Metadata

Authors
Kang, R., Zhu, S., Zeh, H. J., Klionsky, D. J., & Tang, D.
Venue
Autophagy
Published
2018-09-06
Volume
14
Issue
12
Pages
2173-2175
ISSN
  • 1554-8627 (ISSN-L)
  • 1554-8635
OpenAlex
W2889336787
Cited by
189
References
0
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: BECN1 is a new driver of ferroptosis. https://app.cochat.ai/papers/10.1080/15548627.2018.1513758
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Kang, R., Zhu, S., Zeh, H. J., Klionsky, D. J., & Tang, D. (2018). BECN1 is a new driver of ferroptosis. Autophagy. https://doi.org/10.1080/15548627.2018.1513758

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