Evidence map›Paper›PMID 29335367›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2018

Evolution of telomere maintenance and tumour suppressor mechanisms across mammals.

Xiao Tian, Katherine Doerig, Rosa Park, Alice Can Ran Qin, Chaewon Hwang, Alexander Neary, Michael Gilbert, Andrei Seluanov, Vera Gorbunova

Open access · bronzeAbstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

45 citing papers in PubMed, 120 citations in OpenAlex.

  1. Article
  2. Review
  3. Short- and long-term costs of reproduction revealed by telomere dynamics in wild greater horseshoe bats.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  9. DNA repair and anti-cancer mechanisms in the long-lived bowhead whale.bioRxiv : the preprint server for biology · 2024
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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

9 authors at 1 institution in 1 country.

Xiao TianDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.ORCID 0000-0001-5300-3596
Katherine DoerigDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.
Rosa ParkDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.
Alice Can Ran QinDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.
Chaewon HwangDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.
Alexander NearyDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.
Michael GilbertDepartment of Biology, University of Rochester, Rochester, NY 14627, USA.
Andrei SeluanovDepartment of Biology, University of Rochester, Rochester, NY 14627, USA andrei.seluanov@rochester.edu.
Vera GorbunovaDepartment of Biology, University of Rochester, Rochester, NY 14627, USA vera.gorbunova@rochester.edu.ORCID 0000-0001-8979-0333
Google (United States) · US

Funding

The role of hyaluronan in longevity and cancer resistance of longest-lived rodentP01AG047200 · NIA · UNIVERSITY OF ROCHESTER · PI Vera Gorbunova · 2014 to 2026
$36.9M
The role of SIRT6 posttranslational modifications in aging and genome stability. Supplement: Testing SIRT6 activators as potential Alzheimer's disease therapy.R01AG027237 · NIA · UNIVERSITY OF ROCHESTER · PI Vera Gorbunova · 2006 to 2026
$6.2M
Comparative analysis of IGF-1 and mTOR signaling in short- and long-lived rodentsR03AG052365 · NIA · UNIVERSITY OF ROCHESTER · PI GORBUNOVA, VERA · 2016 to 2017
$154k
NIA NIH HHS P01 AG047200NIA NIH HHS R01 AG027237NIA NIH HHS R03 AG052365
6 · The paper itself

Abstract

Mammalian species differ dramatically in telomere biology. Species larger than 5-10 kg repress somatic telomerase activity and have shorter telomeres, leading to replicative senescence. It has been proposed that evolution of replicative senescence in large-bodied species is an anti-tumour mechanism counteracting increased risk of cancer due to increased cell numbers. By contrast, small-bodied species express high telomerase activity and have longer telomeres. To counteract cancer risk due to longer lifespan, long-lived small-bodied species evolved additional telomere-independent tumour suppressor mechanisms. Here, we tested the connection between telomere biology and tumorigenesis by analysing the propensity of fibroblasts from 18 rodent species to form tumours. We found a negative correlation between species lifespan and anchorage-independent growth. Small-bodied species required inactivation of Rb and/or p53 and expression of oncogenic H-Ras to form tumours. Large-bodied species displayed a continuum of phenotypes requiring additional genetic 'hits' for malignant transformation. Based on these data we refine the model of the evolution of tumour suppressor mechanisms and telomeres. We propose that two different strategies evolved in small and large species because small-bodied species cannot tolerate small tumours that form prior to activation of the telomere barrier, and must instead use telomere-independent strategies that act earlier, at the hyperplasia stage.This article is part of the theme issue 'Understanding diversity in telomere dynamics'.

Indexed as

Evolution, MolecularTelomere HomeostasisAnimalsCarcinogenesisCellular SenescenceFibroblastsGenes, p53Genes, rasGenes, RetinoblastomaHumansMice, NudePrimary Cell CultureRodentiaSkinTelomeraseTelomereTelomeraseageingcancerevolutionlifespanmammalstelomeres

Identifiers

PMID29335367
PMCPMC5784063
OpenAlexW2783543687

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.