Evidence map›Paper›PMID 22975007›Full record

ReviewCurrent biology : CB2012

Cancer in light of experimental evolution.

Kathleen Sprouffske, Lauren M F Merlo, Philip J Gerrish, Carlo C Maley, Paul D Sniegowski

Abstract readReview
In one paragraph

Review in Current biology : CB, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Journal of bacteriology · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Synthetic hybrids of six yeast species.Nature communications · 2020
    Article
  11. Article
  12. Article
  13. DNA Damage Stress: Cui Prodest?International journal of molecular sciences · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

5 authors.

Kathleen SprouffskeInstitute for Evolutionary Biology and Environmental Sciences, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland. kathleen.sprouffske@ieu.uzh.ch
Lauren M F Merlo
Philip J Gerrish
Carlo C Maley
Paul D Sniegowski

Funding

PHYLOGENIES of Barrett's Esophagus LineagesP01CA091955 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GRADY, WILLIAM MALLORY · 2002 to 2019
$35.9M
Modeling Neoplastic Progression in Barrett's Esophagus - Renewal -2R01CA140657 · NCI · WISTAR INSTITUTE · PI Carlo Maley · 2009 to 2026
$5.0M
Stem Cells, Differentiation and Therapeutic Resistance in AMLR01CA149566 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CARROLL, MARTIN · 2011 to 2015
$3.0M
Mutation rate catastrophe: testing a novel theory for the extinction of clonal orR01GM079483 · NIGMS · UNIVERSITY OF NEW MEXICO · PI GERRISH, PHILIP JOHN · 2008 to 2010
$1.1M
The specialized role of Hsp70 in protein importF32GM079843 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI LEE, THOMAS · 2007 to 2008
$99k
NCI NIH HHS P01 CA091955NCI NIH HHS P01 CA91955NCI NIH HHS R01 CA140657NCI NIH HHS R01 CA149566NIGMS NIH HHS F32 GM079843NIGMS NIH HHS R01 GM079483NIGMS NIH HHS R01 GM079843-01PHS HHS 35063
6 · The paper itself

Abstract

Cancer initiation, progression, and the emergence of therapeutic resistance are evolutionary phenomena of clonal somatic cell populations. Studies in microbial experimental evolution and the theoretical work inspired by such studies are yielding deep insights into the evolutionary dynamics of clonal populations, yet there has been little explicit consideration of the relevance of this rapidly growing field to cancer biology. Here, we examine how the understanding of mutation, selection, and spatial structure in clonal populations that is emerging from experimental evolution may be applicable to cancer. Along the way, we discuss some significant ways in which cancer differs from the model systems used in experimental evolution. Despite these differences, we argue that enhanced prediction and control of cancer may be possible using ideas developed in the context of experimental evolution, and we point out some prospects for future research at the interface between these traditionally separate areas.

Indexed as

Evolution, MolecularBiological EvolutionDrug Resistance, NeoplasmGenetic VariationHumansModels, BiologicalMutagenesisNeoplasmsSelection, GeneticTumor Microenvironment

Identifiers

PMID22975007
PMCPMC3457634

What OpenQuestion holds

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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.