There are 5 papers on MIR-155-5P in aging research: 2 observational studies in people, 3 in animals.
5 papers study it5 findings
See all 5 papers on MIR-155-5P
At a glance
The findings reach mice, none yet in people. 3 independent labs in 2 countries.
None of its findings points the other way.
- 3 independent labs in 2 countries
- Funders: American Heart Association and others
- 2 of 5 findings with company ties
- Humans2
- Animals3
Effects
5mTOR signaling pathway components
downin mice1
1 study
mTOR signaling pathway components
downin mice1
MIR-155-5P inhibits mTOR signaling pathway components in mice.
“and target mTOR signaling pathway components and other cellular communication pathways”
Animals
Nature communications
Brain expression with age
upin mice1
1 study
Brain expression with age
upin mice1
MIR-155-5P increases brain expression with age in mice (sex-independent).
“We identified three sex-independent brain aging microRNAs (miR-146a-5p, miR-155-5p, and miR-5100).”
Animalssex-independentbrain
Nature communications
SIRT1
downin cells1
1 study
SIRT1
downin cells1
MIR-155-5P inhibits SIRT1 in cells (alcohol exposure).
“miR-155-5p targets and inhibits SIRT1, promoting the expression of mitochondrial VDAC1”
Cellsalcohol exposureliver
Phytomedicine : international journal of phytotherapy and phytopharmacology
CAB39
downin human cells1
1 study
CAB39
downin human cells1
MIR-155-5P decreases CAB39 in human cells (via AMPK signaling).
“miR-155-5p inhibited mitochondrial fission and increased mitochondrial fusion in MSCs via the AMPK signaling pathway, thereby resulting in cellular senescence by repressing the expression of Cab39”
Cellsvia AMPK signalingmesenchymal stem cells
Aging cell
Cellular senescence
upin human cells1
1 study
Cellular senescence
upin human cells1
MIR-155-5P increases cellular senescence in human cells (upregulation in young MSCs; downregulation in aged MSCs).
“Upregulation of miR-155-5p in YMSCs led to increased cellular senescence, whereas downregulation of miR-155-5p decreased AMSC senescence.”
Cellsupregulation in young MSCs; downregulation in aged MSCsmesenchymal stem cells
Aging cell