Evidence map›Paper›PMID 28069394›Full record

ReviewBiochimica et biophysica acta. Reviews on cancer2017

Catch my drift? Making sense of genomic intra-tumour heterogeneity.

Andrea Sottoriva, Chris P Barnes, Trevor A Graham

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Reviews on cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Advances in Colorectal Cancer Cell Biology and Clonal Evolution.International journal of molecular sciences · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Mutation divergence over space in tumour expansion.Journal of the Royal Society, Interface · 2023
    Article
  8. Tumour Genetic Heterogeneity in Relation to Oral Squamous Cell Carcinoma and Anti-Cancer Treatment.International journal of environmental research and public health · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Big Bang Tumor Growth and Clonal Evolution.Cold Spring Harbor perspectives in medicine · 2018
    Review
  20. Review
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.

Andrea SottorivaCentre for Evolution and Cancer, The Institute of Cancer Research, London, SM2 5NG, UK. Electronic address: andrea.sottoriva@icr.ac.uk.
Chris P BarnesDepartment of Cell and Developmental Biology, University College London, London, UK. Electronic address: christopher.barnes@ucl.ac.uk.
Trevor A GrahamEvolution and Cancer Laboratory, Barts Cancer Institute, Charterhouse Sq, Queen Mary University of London, EC1M 6BQ, UK. Electronic address: t.graham@qmul.ac.uk.

Funding

Cancer Research UK 19771Wellcome Trust
6 · The paper itself

Abstract

The cancer genome is shaped by three components of the evolutionary process: mutation, selection and drift. While many studies have focused on the first two components, the role of drift in cancer evolution has received little attention. Drift occurs when all individuals in the population have the same likelihood of producing surviving offspring, and so by definition a drifting population is one that is evolving neutrally. Here we focus on how neutral evolution is manifested in the cancer genome. We discuss how neutral passenger mutations provide a magnifying glass that reveals the evolutionary dynamics underpinning cancer development, and outline how statistical inference can be used to quantify these dynamics from sequencing data. We argue that only after we understand the impact of neutral drift on the genome can we begin to make full sense of clonal selection. This article is part of a Special Issue entitled: Evolutionary principles - heterogeneity in cancer? Edited by Dr. Robert A. Gatenby.

Indexed as

Evolution, MolecularGenetic DriftGenetic FitnessGenetic HeterogeneityAdaptation, PhysiologicalAnimalsBiomarkers, TumorCell Transformation, NeoplasticGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseGenomicsHeredityHumansModels, GeneticMutationNeoplasmsBiomarkers, TumorClonal evolution of cancerClonesIntra-tumour heterogeneityNeutral evolutionNext generation sequencingSelection

Identifiers

PMID28069394
PMCPMC5446319

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.