Evidence map›Paper›PMID 26056356›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2015

Towards cancer-aware life-history modelling.

Hanna Kokko, Michael E Hochberg

Abstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. The occurrence of cancer in vertebrates: a mini review.Journal of biological research (Thessalonike, Greece) · 2020
    Review
  5. Article
  6. Review
  7. Lifetime cancer prevalence and life history traits in mammals.Evolution, medicine, and public health · 2020
    Article
  8. All's well that ends well: why large species have short telomeres.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Article
  9. DNA helix: the importance of being AT-rich.Mammalian genome : official journal of the International Mammalian Genome Society · 2017
    Article
  10. Size, longevity and cancer: age structure.Proceedings. Biological sciences · 2016
    Article
  11. Peto's paradox and the promise of comparative oncology.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Article
  12. Inclusive fitness effects can select for cancer suppression into old age.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Article
  13. Peto's paradox and human cancers.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    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

2 authors.

Hanna KokkoWissenschaftskolleg zu Berlin, Institute for Advanced Study, Wallotstrasse 19, Berlin 14193, Germany Institute of Evolutionary Biology and Environmental Studies, University of Zurich, Winterthurerstrasse 190, Zurich 8057, Switzerland hanna.kokko@ieu.uzh.ch.
Michael E HochbergWissenschaftskolleg zu Berlin, Institute for Advanced Study, Wallotstrasse 19, Berlin 14193, Germany Institut des Sciences de l'Evolution, Université Montpellier, UMR5554 du CNRS, Montpellier 34095, France Santa Fe Institute, 1399 Hyde Park Road, Santa Fe, NM 87501, USA mhochber@univ-montp2.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies of body size evolution, and life-history theory in general, are conducted without taking into account cancer as a factor that can end an organism's reproductive lifespan. This reflects a tacit assumption that predation, parasitism and starvation are of overriding importance in the wild. We argue here that even if deaths directly attributable to cancer are a rarity in studies of natural populations, it remains incorrect to infer that cancer has not been of importance in shaping observed life histories. We present first steps towards a cancer-aware life-history theory, by quantifying the decrease in the length of the expected reproductively active lifespan that follows from an attempt to grow larger than conspecific competitors. If all else is equal, a larger organism is more likely to develop cancer, but, importantly, many factors are unlikely to be equal. Variations in extrinsic mortality as well as in the pace of life--larger organisms are often near the slow end of the fast-slow life-history continuum--can make realized cancer incidences more equal across species than what would be observed in the absence of adaptive responses to cancer risk (alleviating the so-called Peto's paradox). We also discuss reasons why patterns across species can differ from within-species predictions. Even if natural selection diminishes cancer susceptibility differences between species, within-species differences can remain. In many sexually dimorphic cases, we predict males to be more cancer-prone than females, forming an understudied component of sexual conflict.

Indexed as

Models, BiologicalAnimalsBiological EvolutionBody SizeFemaleHumansLongevityMaleNeoplasmsReproductionRisk FactorsSelection, GeneticSpecies Specificitybody sizecancercoevolutionlife historyPeto′s paradoxsexual conflict

Identifiers

PMID26056356
PMCPMC4581035

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.