Unlocking Mitochondrial Dysfunction-Associated Senescence (MiDAS) with NAD + - a Boolean Model of Mitochondrial Dynamics and Cell Cycle Control.
Herbert SizekDávid DeriteiKatherine FleigMarlayna HarrisPeter L ReganKimberly GlassErzsébet Ravasz ReganPublished in: bioRxiv : the preprint server for biology (2024)
Boolean regulatory network model reproduces mitochondrial dynamics during cell cycle progression, apoptosis, and glucose starvation. Model offers a mechanistic explanation for the positive feedback loop that locks in Mitochondrial Dysfunction-Associated Senescence (MiDAS), involving autophagy-resistant, hyperfused, dysfunctional mitochondria. Model reproduces ROS-mediated mitochondrial dysfunction and suggests that MiDAS is part of the early phase of damage-induced senescence. Model predicts that cancer-driving mutations that bypass the G1/S checkpoint generally increase the incidence of MiDAS, except for p53 loss.
Keyphrases
- cell cycle
- oxidative stress
- dna damage
- cell proliferation
- cell death
- endothelial cells
- transcription factor
- endoplasmic reticulum stress
- type diabetes
- squamous cell carcinoma
- signaling pathway
- stress induced
- metabolic syndrome
- diabetic rats
- young adults
- high glucose
- weight loss
- papillary thyroid
- lymph node metastasis