Long-term depletion of cereblon induces mitochondrial dysfunction in cancer cells

长期消耗 cereblon 会导致癌细胞线粒体功能障碍

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作者:Seulki Park, Kidae Kim, Keeok Haam, Hyun Seung Ban, Jung-Ae Kim, Byoung Chul Park, Sung Goo Park, Sunhong Kim, Jeong-Hoon Kim

Abstract

Cereblon (CRBN) is a multi-functional protein that acts as a substrate receptor of the E3 ligase complex and a molecular chaperone. While CRBN is proposed to function in mitochondria, its specific roles are yet to be established. Here, we showed that knockdown of CRBN triggers oxidative stress and calcium overload in mitochondria, leading to disruption of mitochondrial membrane potential. Notably, long-term CRBN depletion using PROteolysis TArgeting Chimera (PROTAC) induced irreversible mitochondrial dysfunction, resulting in cell death. Our collective findings indicate that CRBN is required for mitochondrial homeostasis in cells. [BMB Reports 2021; 54(6): 305-310].

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