The broccoli derivative sulforaphane extends lifespan by slowing the transcriptional aging clock
Sedore, C. A.; Segerdell, E.; Coleman-Hulbert, A. L.; Johnson, E.; Levi, J. N.; Lithgow, G. J.; Driscoll, M.; Phillips, P. C.
Show abstract
Sulforaphane, an organosulfur isothiocyanate derived from cruciferous vegetables, has been shown to inhibit inflammation, oxidative stress, and cancer cell growth. To explore the potential of sulforaphane as a candidate natural compound for promoting longevity more generally, we tested the dose and age-specific effects of sulforaphane on C. elegans longevity, finding that it can extend lifespan by more than 50% at the most efficacious doses, but that treatment must be initiated early in life to be effective. We then created a novel, gene-specific, transcriptional aging clock, which demonstrated that sulforaphane-treated individuals exhibited a "transcriptional age" that was approximately four days younger than age-matched controls, representing a nearly 20% reduction in biological age. The clearest transcriptional responses were detoxification pathways, which, together with the shape of the dose-response curve, indicates a likely hormetic response to sulforaphane. These results support the idea that robust longevity-extending interventions can act via global effects across the organism, as revealed by systems level changes in gene expression.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Age-Invariant Genes: Multi-Tissue Identification and Characterization of Murine Reference Genes 96%
- The coupling between healthspan and lifespan in Caenorhabditis depends on complex interactions between compound intervention and genetic background 96%
- Combining Stem Cell Rejuvenation and Senescence Targeting to Synergistically Extend Lifespan 94%
Similar papers in this journal
- Cyrene: A Novel Geroprotective Compound that Extends Lifespan and Healthspan in C. elegans and Drosophila 96%
- A hierarchy of causes of death in senescent C. elegans 94%
- Divergent patterns of healthy aging across human brain regions at single-cell resolution reveal links to neurodegenerative disease 93%
Similar papers in this journal
- Regulation of defective mitochondrial DNA accumulation and transmission in C. elegans by the programmed cell death and aging pathways 95%
- The HPA stress axis shapes aging rates in long-lived, social mole-rats 95%
- Computer prediction and genetic analysis identifies retinoic acid modulation as a driver of conserved longevity pathways in genetically-diverse Caenorhabditis nematodes 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.