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Updated: Mar 24, 2026

Monitoring Stub1-Mediated Pexophagy
Published on: May 12, 2023
The peroxisome as a cell signaling organelle
Durga Nand Tripathi1, Cheryl Lyn Walker1
1Center for Translational Cancer Research, Institute of Bioscience & Technology, Texas A&M University Health Science Center, Houston, TX 77030, United States.
Abstract:
Peroxisomes participate in lipid metabolism, and are a major source of ROS in the cell. Their importance in cellular energy balance and redox homeostasis is well-established, as is the need to maintain peroxisome homeostasis to prevent pathologies associated with too few, or too many, of these organelles. How cells regulate peroxisome number has remained somewhat elusive. Recently, the tumor suppressors ATM and TSC, which regulate mTORC1 signaling, have been localized to peroxisomes. When activated by peroxisomal ROS, ATM signals to TSC to repress mTORC1 signaling and increase autophagic flux in cells, and also phosphorylates the peroxisomal protein PEX 5 to target peroxisomes for selective autophagy (pexophagy), providing a mechanism for regulation of peroxisomal homeostasis using ROS as a rheostat.
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