Senescence-associated marker expression
2 papers2 findings
- Humans1
- Cells1
Interventions
2Substrate stiffness
upin human cells1
1 study
Substrate stiffness
upin human cells1
Substrate stiffness increases senescence-associated marker expression in human cells.
“increasing substrate stiffness enhanced fibroblast spreading, stress fiber thickening, focal adhesion maturation, cellular stiffness, and senescence-associated marker expression.”
Cellsincreasing substrate stiffnesstunable polyacrylamide hydrogelsfibroblast
SERPINE1–AP2A1 interplay links substrate stiffness to fibroblast senescence
bioRxiv (Cold Spring Harbor Laboratory)1 Jul 2026Preprint
Etoposide
no changein mouse cells1
1 study
Etoposide
no changein mouse cells1
Etoposide has no effect on senescence-associated marker expression in mouse cells.
“While DNA damage increased after treatment, after 24 h, no change in the expression of senescence-associated markers was observed.”
CellsEtoposide-induced DNA damageprimary neuron24 h
DNA Damage and Senescence in the Aging and Alzheimer's Disease Cortex Are Not Uniformly Distributed
Biomedicines14 Jun 2024
Latest
2 in 12 monthsbioRxiv
SERPINE1–AP2A1 interplay links substrate stiffness to fibroblast senescence
Preprint: experiments in human cellsCellular senescence
The American Journal of Dermatopathology
Dermal Interstitial Glycogenosis and Stromal Senescence-Associated Marker Expression in Fibrofolliculomas: Implications for Pathogenesis and mTOR-Targeted Therapy
Study in peopleMechanisms
Journal of Translational Medicine
Macrophage derived VEGF regulates macrophage senescence to inhibit radiation-induced dermatitis
Experiments in miceVEGF signalling
Journal of Nanobiotechnology
Young fibroblast-derived migrasomes alleviate keratinocyte senescence and enhance wound healing in aged skin
Experiments in animalsInterventions
Biomedicines
DNA Damage and Senescence in the Aging and Alzheimer's Disease Cortex Are Not Uniformly Distributed
Case-control study in peopleDNA damage response