Evidence map›Paper›PMID 23863708›Full record

ArticleThe Journal of clinical investigation2013

Rapamycin extends murine lifespan but has limited effects on aging.

Frauke Neff, Diana Flores-Dominguez, Devon P Ryan, Marion Horsch, Susanne Schröder, Thure Adler, Luciana Caminha Afonso, Juan Antonio Aguilar-Pimentel, Lore Becker, Lillian Garrett and 30 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 237 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
237citing papers in PubMed, 2 pooled it
16.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

237 citing papers in PubMed, 2 syntheses or guidelines pooled it, 372 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Autophagy modulation in cancer.Nature reviews. Drug discovery · 2026
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177 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

40 authors at 13 institutions in 2 countries.

Frauke NeffInstitute of Pathology, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Diana Flores-Dominguez
Devon P Ryan
Marion Horsch
Susanne Schröder
Thure Adler
Luciana Caminha Afonso
Juan Antonio Aguilar-Pimentel
Lore Becker
Lillian Garrett
Wolfgang Hans
Moritz M Hettich
Richard Holtmeier
Sabine M Hölter
Kristin Moreth
Cornelia Prehn
Oliver Puk
Ildikó Rácz
Birgit Rathkolb
Jan Rozman
Beatrix Naton
Rainer Ordemann
Jerzy Adamski
Johannes Beckers
Raffi Bekeredjian
Dirk H Busch
Gerhard Ehninger
Jochen Graw
Heinz Höfler
Martin Klingenspor
Thomas Klopstock
Markus Ollert
Jörg Stypmann
Eckhard Wolf
Wolfgang Wurst
Andreas Zimmer
Helmut Fuchs
Valérie Gailus-Durner
Martin Hrabe de Angelis
Dan Ehninger
Helmholtz Zentrum München · DEHelmholtz Association of German Research Centres · DEGerman Center for Neurodegenerative Diseases · DEUniversity Hospital Carl Gustav Carus · DEUniversity of Bonn · DEUniversity of Minnesota · USHeidelberg University · DEInstitute of Medical Microbiology and Hygiene · DELudwig-Maximilians-Universität München · DEMax Planck Society · DEMünchen Klinik · DETechnical University of Munich · DEWeihenstephan-Triesdorf University of Applied Sciences · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging is a major risk factor for a large number of disorders and functional impairments. Therapeutic targeting of the aging process may therefore represent an innovative strategy in the quest for novel and broadly effective treatments against age-related diseases. The recent report of lifespan extension in mice treated with the FDA-approved mTOR inhibitor rapamycin represented the first demonstration of pharmacological extension of maximal lifespan in mammals. Longevity effects of rapamycin may, however, be due to rapamycin's effects on specific life-limiting pathologies, such as cancers, and it remains unclear if this compound actually slows the rate of aging in mammals. Here, we present results from a comprehensive, large-scale assessment of a wide range of structural and functional aging phenotypes, which we performed to determine whether rapamycin slows the rate of aging in male C57BL/6J mice. While rapamycin did extend lifespan, it ameliorated few studied aging phenotypes. A subset of aging traits appeared to be rescued by rapamycin. Rapamycin, however, had similar effects on many of these traits in young animals, indicating that these effects were not due to a modulation of aging, but rather related to aging-independent drug effects. Therefore, our data largely dissociate rapamycin's longevity effects from effects on aging itself.

Indexed as

AgingAnimalsCell Transformation, NeoplasticDrug Evaluation, PreclinicalGranulomaImmunoglobulinsLeukocyte CountLiverLiver CirrhosisLongevityMaleMaze LearningMiceMice, Inbred C57BLMuscle StrengthOxygen ConsumptionImmunoglobulinsmTOR protein, mouseSirolimusTOR Serine-Threonine Kinases

Identifiers

PMID23863708
PMCPMC3726163
OpenAlexW2025133084

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.