Evidence map›Paper›PMID 40983796›Full record

ReviewCancer metastasis reviews2025

Targeting developmental vulnerabilities in childhood sarcomas.

Elise Young, Barnaby Kelly, Jason E Cain

Abstract readReview
In one paragraph

Review in Cancer metastasis reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Translational cancer research · 2026
    Article
  2. On the origins of childhood cancer.Cancer metastasis reviews · 2026
    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

3 authors.

Elise Young *Hudson Institute of Medical Research, 27-31 Wright St, Clayton, Victoria, 3168, Australia.
Barnaby Kelly *Hudson Institute of Medical Research, 27-31 Wright St, Clayton, Victoria, 3168, Australia.
Jason E CainHudson Institute of Medical Research, 27-31 Wright St, Clayton, Victoria, 3168, Australia. jason.cain@hudson.org.au.

Funding

National Health and Medical Research Council APP2028353
6 · The paper itself

Abstract

Childhood sarcomas are an aggressive and diverse group of mesenchymal-origin malignancies that collectively account for over a third of paediatric solid tumours. There has been little progress made in the treatment of childhood sarcomas in recent decades, and survival outcomes are poor compared to most other common paediatric cancers. Furthermore, long-term survivors of childhood sarcomas face disproportionately high morbidity from treatment. A unique feature of paediatric and adolescent sarcomas, compared to adult-type sarcomas, is that they arise from developing tissues and often share features with tissue-specific progenitors suggesting that they originate from cells that are arrested in a primitive developmental window. The developmental origins of paediatric sarcomas are also reflected in the incidence of different sarcoma types which correlate with age-specific tissue expansion and growth. In this review, we discuss the molecular mechanisms underpinning paediatric sarcomagenesis, focusing on how distortion of normal developmental programming, such as epigenetic regulation, embryonic signalling pathways, and aberrant growth pathways, contributes to childhood sarcoma development and progression. Finally, we will review the new and emerging therapeutic strategies seeking to target these developmental vulnerabilities.

Indexed as

SarcomaAnimalsChildEpigenesis, GeneticHumansSignal TransductionChildhood cancerDevelopmental pathwaysSarcomaSignallingTherapeutics

Identifiers

PMID40983796
PMCPMC12454515

What OpenQuestion holds

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LicenceCC BY
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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.