Evidence map›Paper›PMID 38848676›Full record

ReviewCell2024

A developmental constraint model of cancer cell states and tumor heterogeneity.

Ayushi S Patel, Itai Yanai

Abstract readReview
In one paragraph

Review in Cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Review
  2. Genes, fuel, and fate in lung cancer.Biochemical Society transactions · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Unveiling the developmental and tumor-suppressive roles of the p53 variant p53psi.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  18. Article
  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

2 authors.

Ayushi S PatelInstitute for Systems Genetics, NYU Grossman School of Medicine, New York, NY, USA; Department of Biochemistry & Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY, USA; Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
Itai YanaiInstitute for Systems Genetics, NYU Grossman School of Medicine, New York, NY, USA; Department of Biochemistry & Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY, USA; Perlmutter Cancer Center, NYU Langone Health, New York, NY, USA. Electronic address: itai.yanai@nyulangone.org.

Funding

Project 3: The Evolving Role of Regional Lymph Nodes in Melanoma ProgressionU54CA263001 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Eva Hernando, Iman Osman · 2022 to 2026
$11.6M
Identification and characterization of cancer cell states by novel computational and experimental technologies - Resubmission - 1U01CA260432 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Richard Mark White, ITAI YANAI · 2022 to 2026
$2.9M
Computational approaches for the systematic detection of cell-cell interactions by spatial transcriptomics - Resubmission - 1R01LM013522 · NLM · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI YANAI, ITAI · 2021 to 2024
$1.4M
Inferring cell state tumor microenvironment maps by integrating single-cell and spatial transcriptomicsR21CA264361 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI YANAI, ITAI · 2021 to 2022
$516k
NCI NIH HHS R21 CA264361NCI NIH HHS U01 CA260432NCI NIH HHS U54 CA263001NLM NIH HHS R01 LM013522
6 · The paper itself

Abstract

Cancer is a disease that stems from a fundamental liability inherent to multicellular life forms in which an individual cell is capable of reneging on the interests of the collective organism. Although cancer is commonly described as an evolutionary process, a less appreciated aspect of tumorigenesis may be the constraints imposed by the organism's developmental programs. Recent work from single-cell transcriptomic analyses across a range of cancer types has revealed the recurrence, plasticity, and co-option of distinct cellular states among cancer cell populations. Here, we note that across diverse cancer types, the observed cell states are proximate within the developmental hierarchy of the cell of origin. We thus posit a model by which cancer cell states are directly constrained by the organism's "developmental map." According to this model, a population of cancer cells traverses the developmental map, thereby generating a heterogeneous set of states whose interactions underpin emergent tumor behavior.

Indexed as

Models, BiologicalNeoplasmsAnimalsCarcinogenesisHumansNeoplastic Stem CellsSingle-Cell AnalysisTranscriptomecancer cell statescellular plasticitydevelopmental constraintstumor heterogeneitytumorigenesis

Identifiers

PMID38848676
PMCPMC11256907

What OpenQuestion holds

Textmetadata
LicenceTDM
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.