LNCAAT

There is 1 paper on LNCAAT in aging research: none in people yet, 1 in animals. The newest story, Oct 31, 2026: “Removing an RNA delayed blood vessel aging in mice”.

Gene

1 paper studies it3 findings

1 new paper in 30 daysSee all 1

None of its findings points the other way.

  • 1 lab in 1 country
  • Animals1

Effects

3

Energy production

downin mice1

1 study
  1. LNCAAT decreases energy production in mice (lncAAT overexpression).

    “LncAAT overexpression mediated fall in energy production led to endothelial senescence in vivo and in vitro.”

    AnimalslncAAT overexpressionvascular endothelium

    Removing an RNA delayed blood vessel aging in mice

    Cardiovascular research

endothelial senescence

upin mice1

1 study
  1. LNCAAT induces endothelial senescence in mice (lncAAT overexpression).

    “LncAAT overexpression mediated fall in energy production led to endothelial senescence in vivo and in vitro.”

    AnimalslncAAT overexpressionvascular endothelium

    Removing an RNA delayed blood vessel aging in mice

    Cardiovascular research

Endothelial-mediated vasodilation

downin mice1

1 study
  1. LNCAAT impairs endothelial-mediated vasodilation in mice (shown by endothelial-specific knockout).

    “Endothelial-specific knockout of lncAAT in mice delayed vascular aging, enhanced endothelial-mediated vasodilation, and improved angiogenesis in a hindlimb-ischemia model.”

    Animalsshown by endothelial-specific knockoutvascular endothelium

    Removing an RNA delayed blood vessel aging in mice

    Cardiovascular research

Latest

Dec 2025: 0Jan 2026: 0Feb 2026: 0Mar 2026: 0Apr 2026: 0May 2026: 0Jun 2026: 0Jul 2026: 0Aug 2026: 0Sep 2026: 0Oct 2026: 1Nov 2026: 01 paper in 12 months
Cardiovascular Research

Removing an RNA delayed blood vessel aging in mice

Deleting the RNA from cells lining mouse blood vessels also improved vessel widening and new blood vessel growth in a model of restricted blood flow.Deleting the RNA from cells lining mouse blood vessels also improved vessel widening and new blood vessel growth in a model of restricted blood flow.

Mouse studyMechanisms