Evidence map›Paper›PMID 26046760›Full record

ReviewCell stem cell2015

Aging-Induced Stem Cell Mutations as Drivers for Disease and Cancer.

Peter D Adams, Heinrich Jasper, K Lenhard Rudolph

Open access · hybridAbstract readReview
In one paragraph

Review in Cell stem cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
12.2field-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

100 citing papers in PubMed, 179 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Pandora's Box of AML: HowBiomedicines · 2025
    Review
  7. Article
  8. Review
  9. Article
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  12. Article
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  14. Review
  15. Article
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  17. Review
  18. Article
  19. Wnt Signaling and Aging of the Gastrointestinal Tract.International journal of molecular sciences · 2022
    Review
  20. Review

40 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 3 countries.

Peter D AdamsUniversity of Glasgow and Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
Heinrich JasperBuck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945-1400, USA.
K Lenhard RudolphLeibniz Institute for Age Research - Fritz Lipmann Institute e.V. (FLI), Beutenbergstr. 11, 07745 Jena, Germany. Electronic address: KLRudolph@FLI-Leibniz.de.
Buck Institute for Research on Aging · USLeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEUniversity of Glasgow · GB

Funding

STRUCTURAL BASIS FOR EPIGENETICS IN AGING AND LONGEVITYP01AG031862 · NIA · WISTAR INSTITUTE · PI GARCIA, BENJAMIN A · 2008 to 2022
$28.3M
Nutrient signaling and stem cell maintenance in aging epitheliaR01AG047497 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI JASPER, HEINRICH, KENNEDY, BRIAN K · 2015 to 2019
$3.7M
Regulation of UV-Induced ApoptosisR01EY018177 · NEI · UNIVERSITY OF ROCHESTER · PI JASPER, HEINRICH · 2008 to 2018
$3.1M
Systemic coordination of stress responses by insulin signalingR01AG028127 · NIA · UNIVERSITY OF ROCHESTER · PI JASPER, HEINRICH · 2006 to 2015
$3.0M
Redox Signaling and Stem Cell FunctionR01GM100196 · NIGMS · UNIVERSITY OF ROCHESTER · PI BOHMANN, DIRK, JASPER, HEINRICH · 2012 to 2015
$1.7M
Biotechnology and Biological Sciences Research Council C10652/A16566Cancer Research UK 16566Medical Research Council MR/M000605/1NEI NIH HHS EY018177NEI NIH HHS R01 EY018177NIA NIH HHS AG028127NIA NIH HHS AG031862NIA NIH HHS AG047497NIA NIH HHS P01 AG031862NIA NIH HHS R01 AG028127NIA NIH HHS R01 AG047497NIGMS NIH HHS GM100196NIGMS NIH HHS R01 GM100196
6 · The paper itself

Abstract

Aging is characterized by a decrease in genome integrity, impaired organ maintenance, and an increased risk of cancer, which coincide with clonal dominance of expanded mutant stem and progenitor cell populations in aging tissues, such as the intestinal epithelium, the hematopoietic system, and the male germline. Here we discuss possible explanations for age-associated increases in the initiation and/or progression of mutant stem/progenitor clones and highlight the roles of stem cell quiescence, replication-associated DNA damage, telomere shortening, epigenetic alterations, and metabolic challenges as determinants of stem cell mutations and clonal dominance in aging.

Indexed as

AgingAnimalsEpigenesis, GeneticHumansMutationNeoplasmsStem CellsTelomere Shortening

Identifiers

PMID26046760
PMCPMC4509784
OpenAlexW1950115610

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.