Evidence map›Paper›PMID 28573417›Full record

ReviewBiogerontology2017

Convergent adaptation of cellular machineries in the evolution of large body masses and long life spans.

Eleonora Croco, Silvia Marchionni, Gianluca Storci, Massimiliano Bonafè, Claudio Franceschi, Thomas D Stamato, Christian Sell, Antonello Lorenzini

Open access · hybridAbstract readReview
In one paragraph

Review in Biogerontology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Parallel Selection for Longevity in Mammals and Birds.bioRxiv : the preprint server for biology · 2025
    Article
  3. Review
  4. Article
  5. Obesity May Accelerate the Aging Process.Frontiers in endocrinology · 2019
    Review
  6. Review
  7. Article
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

8 authors at 4 institutions in 2 countries.

Eleonora CrocoDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Silvia MarchionniDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Gianluca StorciDepartment of Specialised Experimental, and Diagnostic Medicine, University of Bologna, Bologna, Italy.
Massimiliano BonafèDepartment of Specialised Experimental, and Diagnostic Medicine, University of Bologna, Bologna, Italy.
Claudio FranceschiDepartment of Specialised Experimental, and Diagnostic Medicine, University of Bologna, Bologna, Italy.
Thomas D StamatoLankenau Institute for Medical Research, Wynnewood, PA, USA.
Christian SellDepartment of Pathology, Drexel University College of Medicine, Philadelphia, PA, USA.
Antonello LorenziniDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy. antonello.lorenzini@unibo.it.ORCID 0000-0001-9615-9697
University of Bologna · ITDrexel University · USInstitute of Neurological Sciences · ITLankenau Institute for Medical Research · US

Funding

Novel models for longevity researchR21AG039799 · NIA · DREXEL UNIVERSITY · PI SELL, CHRISTIAN · 2011 to 2012
$425k
NIA NIH HHS R21 AG039799
6 · The paper itself

Abstract

In evolutionary terms, life on the planet has taken the form of independently living cells for the majority of time. In comparison, the mammalian radiation is a relatively recent event. The common mammalian ancestor was probably small and short-lived. The "recent" acquisition of an extended longevity and large body mass of some species of mammals present on the earth today suggests the possibility that similar cellular mechanisms have been influenced by the forces of natural selection to create a convergent evolution of longevity. Many cellular mechanisms are potentially relevant for extending longevity; in this assay, we review the literature focusing primarily on two cellular features: (1) the capacity for extensive cellular proliferation of differentiated cells, while maintaining genome stability; and (2) the capacity to detect DNA damage. We have observed that longevity and body mass are both positively linked to these cellular mechanisms and then used statistical tools to evaluate their relative importance. Our analysis suggest that the capacity for extensive cellular proliferation while maintaining sufficient genome stability, correlates to species body mass while the capacity to correctly identify the presence of DNA damage seems more an attribute of long-lived species. Finally, our data are in support of the idea that a slower development, allowing for better DNA damage detection and handling, should associate with longer life span.

Indexed as

Biological EvolutionBody SizeLongevityAge FactorsAgingAnimalsCellular SenescenceDNA DamageEnergy MetabolismGenomic InstabilityHumansModels, BiologicalTelomere HomeostasisAgingBody sizeConvergent evolutionDNA damageGenomic stabilityLongevityReplicative senescence

Identifiers

PMID28573417
PMCPMC5514201
OpenAlexW2620841069

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.