Verdict

Baker et al. used the INK-ATTAC transgene to remove p16Ink4a-positive cells in progeroid mice. Lifelong clearance delayed several age-related disorders and late-life clearance slowed existing pathology, establishing a causal mouse-model result—not a drug or human treatment effect.

Study facts

StudyBaker et al., Nature (2011)
Year2011
Model / populationINK-ATTAC transgenic mice on a BubR1 progeroid background.
InterventionAP20187-induced genetic clearance of p16Ink4a-expressing cells.
Sample sizeMultiple experimental cohorts; no single study-wide N
Primary endpointOnset and progression of age-related phenotypes in adipose tissue, skeletal muscle, and eye.
Main findingLifelong clearance delayed the onset of several age-related disorders, and late-life clearance attenuated progression of established disorders.
PMID / DOI / RegistryPMID 22048312; DOI 10.1038/nature10600; Registry not applicable to this study type
○ Evidence tier 6 — Animal healthspan / mechanism study

Record verify: verified against primary source

DesignTransgenic genetic-clearance study (mouse)
NMultiple experimental cohorts; no single study-wide N
PMID22048312
DOI10.1038/nature10600
Citation statusPMID 22048312 and DOI 10.1038/nature10600 verified against PubMed 2026-09-02 (Nature 2011;479(7372):232-236, Baker et al.)

Identifiers: DOI verified; PMID verified; trial registry id not applicable to this study type. Record-level verification and identifier-level status are separate: a record can be fully verified against its primary publication while an identifier that cannot apply to the study type — a trial registry ID for an animal study, for instance — is marked not applicable. No identifier is fabricated, and none is left in a “pending” state.

Five-qualifier claim

Species / populationINK-ATTAC transgenic mice (BubR1 progeroid background).
Exposure, route, scheduleAP20187 inducer to trigger apoptosis in p16-expressing cells.
Comparator / durationVehicle-treated transgenic littermates; lifelong.
Endpoint / numeric resultClearing p16-positive cells delayed onset of age-related changes in adipose tissue, skeletal muscle, and eye.
What it did NOT establishGenetic tool in a progeroid model; not a drug and not a human result.