Evidence map›Paper›PMID 37620552›Full record

ReviewNature ecology & evolution2023

Evolutionary determinants of curability in cancer.

Marcela Braga Mansur, Nandita M deSouza, Rachael Natrajan, Lisa M Abegglen, Joshua D Schiffman, Mel Greaves

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature ecology & evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Mitochondria-Targeted Nanomotor: HAdvanced materials (Deerfield Beach, Fla.) · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. 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

6 authors at 3 institutions in 2 countries.

Marcela Braga MansurCentre for Evolution and Cancer, The Institute of Cancer Research, London, UK.ORCID 0000-0002-4854-2031
Nandita M deSouzaDivision of Radiotherapy and Imaging, The Institute of Cancer Research, London, UK.
Rachael NatrajanThe Breast Cancer Now Toby Robins Research Centre, Division of Breast Cancer, The Institute of Cancer Research, London, UK.ORCID 0000-0002-9987-2946
Lisa M AbegglenDepartment of Pediatrics and Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0003-3607-3001
Joshua D SchiffmanDepartment of Pediatrics and Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.ORCID 0000-0002-6968-7694
Mel GreavesCentre for Evolution and Cancer, The Institute of Cancer Research, London, UK. Mel.Greaves@icr.ac.uk.ORCID 0000-0002-7239-1384
Institute of Cancer Research · GBUniversity of Utah · USNational Health Service · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of drug-resistant cells, most of which have a mutated TP53 gene, prevents curative treatment in most advanced and common metastatic cancers of adults. Yet, a few, rarer malignancies, all of which are TP53 wild type, have high cure rates. In this Perspective, we discuss how common features of curable cancers offer insights into the evolutionary and developmental determinants of drug resistance. Acquired loss of TP53 protein function is the most common genetic change in cancer. This probably reflects positive selection in the context of strong ecosystem pressures including microenvironmental hypoxia. Loss of TP53's functions results in multiple fitness benefits and enhanced evolvability of cancer cells. TP53-null cells survive apoptosis, and tolerate potent oncogenic signalling, DNA damage and genetic instability. In addition, critically, they provide an expanded pool of self-renewing, or stem, cells, the primary units of evolutionary selection in cancer, making subsequent adaptation to therapeutic challenge by drug resistance highly probable. The exceptional malignancies that are curable, including the common genetic subtype of childhood acute lymphoblastic leukaemia and testicular seminoma, differ from the common adult cancers in originating prenatally from embryonic or fetal cells that are developmentally primed for TP53-dependent apoptosis. Plus, they have other genetic and phenotypic features that enable dissemination without exposure to selective pressures for TP53 loss, retaining their intrinsic drug hypersensitivity.

Indexed as

EcosystemNeoplasmsAdultBiological EvolutionHumansTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID37620552
OpenAlexW4386121355

What OpenQuestion holds

Textmetadata
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.