Evidence map›Paper›PMID 37743495›Full record

ReviewBMC ecology and evolution2023

Convergent TP53 loss and evolvability in cancer.

Marcela Braga Mansur, Mel Greaves

Abstract readReview
In one paragraph

Review in BMC ecology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. MedComm · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Mutant TP53 promotes invasion of lung cancer cells by regulating desmoglein 3.Journal of cancer research and clinical oncology · 2024
    Article
  7. Article
  8. Comparative Expression Analysis ofCancer diagnosis & prognosis
    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.

Marcela Braga MansurCentre for Evolution and Cancer, The Institute of Cancer Research, ICR, London, UK.ORCID 0000-0002-4854-2031
Mel GreavesCentre for Evolution and Cancer, The Institute of Cancer Research, ICR, London, UK. Mel.Greaves@icr.ac.uk.ORCID 0000-0002-7239-1384

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cell populations evolve by a stepwise process involving natural selection of the fittest variants within a tissue ecosystem context and as modified by therapy. Genomic scrutiny of patient samples reveals an extraordinary diversity of mutational profiles both between patients with similar cancers and within the cancer cell population of individual patients. Does this signify highly divergent evolutionary trajectories or are there repetitive and predictable patterns?Major evolutionary innovations or adaptations in different species are frequently repeated, or convergent, reflecting both common selective pressures and constraints on optimal solutions. We argue this is true of evolving cancer cells, especially with respect to the TP53 gene. Functional loss variants in TP53 are the most common genetic change in cancer. We discuss the likely microenvironmental selective pressures involved and the profound impact this has on cell fitness, evolvability and probability of subsequent drug resistance.

Indexed as

EcosystemNeoplasmsBiological EvolutionGenomeHumansMutationSelection, GeneticTumor Suppressor Protein p53TP53 protein, humanTumor Suppressor Protein p53cancerconvergencedrug resistancehypoxiastem cellsTP53

Identifiers

PMID37743495
PMCPMC10518978

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.