Evidence map›Paper›PMID 39266532›Full record

ArticleNature communications2024

Cellular origin and clonal evolution of human dedifferentiated liposarcoma.

Nadège Gruel, Chloé Quignot, Laëtitia Lesage, Sophie El Zein, Sylvie Bonvalot, Dimitri Tzanis, Khadija Ait Rais, Fabien Quinquis, Bastien Manciot, Julien Vibert and 14 more

Abstract read
In one paragraph

Article in Nature communications, 2024. 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. Trial
  2. Review
  3. Article
  4. Dedifferentiated Liposarcoma of the Right Colon.Digestive diseases and sciences · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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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

24 authors.

Nadège GruelINSERM U830, Diversity and Plasticity of Childhood Tumors Lab, PSL Research University, Institut Curie Research Center, Paris, France.ORCID 0000-0001-6915-8082
Chloé Quignot *INSERM U830, Diversity and Plasticity of Childhood Tumors Lab, PSL Research University, Institut Curie Research Center, Paris, France.
Laëtitia Lesage *Department of Pathology, Institut Curie Hospital, Paris, France.ORCID 0000-0001-8592-2482
Sophie El ZeinDepartment of Pathology, Institut Curie Hospital, Paris, France.
Sylvie BonvalotDepartment of Surgical Oncology, Institut Curie Hospital, Paris, France.ORCID 0000-0001-9726-9732
Dimitri TzanisDepartment of Surgical Oncology, Institut Curie Hospital, Paris, France.
Khadija Ait RaisDepartment of Genetics, Institut Curie Hospital, Paris, France.
Fabien QuinquisDepartment of Genetics, Institut Curie Hospital, Paris, France.
Bastien ManciotINSERM U830, Diversity and Plasticity of Childhood Tumors Lab, PSL Research University, Institut Curie Research Center, Paris, France.
Julien VibertINSERM U830, Diversity and Plasticity of Childhood Tumors Lab, PSL Research University, Institut Curie Research Center, Paris, France.
Nadine El TannirMedico Scientific Program for Adult sarcomas, Institut Curie Research Center, Paris, France.
Ahmed DahmaniLaboratory of Preclinical Investigation, Department of translational Research, PSL Research University, Institut Curie Research Center, Paris, France.
Héloïse DerrienLaboratory of Preclinical Investigation, Department of translational Research, PSL Research University, Institut Curie Research Center, Paris, France.
Didier DecaudinLaboratory of Preclinical Investigation, Department of translational Research, PSL Research University, Institut Curie Research Center, Paris, France.
Ivan BiècheDepartment of Genetics, Institut Curie Hospital, Paris, France.
Laura CourtoisDepartment of Genetics, Institut Curie Hospital, Paris, France.
Odette MarianiDepartment of Pathology, Institut Curie Hospital, Paris, France.ORCID 0000-0002-3517-4399
Laëtitia K LinaresINSERM U1194, Metabolism and Sarcoma, Institut de Recherche en Cancérologie de Montpellier, Université de Montpellier, Montpellier, France.ORCID 0000-0003-1661-2119
Laurie GayteINSERM U1194, Metabolism and Sarcoma, Institut de Recherche en Cancérologie de Montpellier, Université de Montpellier, Montpellier, France.ORCID 0009-0007-4742-9823
Sylvain BaulandeInstitut Curie Genomics of Excellence (ICGex) Platform, PSL Research University, Institut Curie, Paris, France.ORCID 0000-0003-3104-1684
Joshua J WaterfallDepartment of Translational Research, Institut Curie Research Center, Paris, France.ORCID 0000-0002-3762-5050
Olivier DelattreINSERM U830, Diversity and Plasticity of Childhood Tumors Lab, PSL Research University, Institut Curie Research Center, Paris, France.ORCID 0000-0002-8730-2276
Gaëlle PierronDepartment of Genetics, Institut Curie Hospital, Paris, France.ORCID 0000-0002-2536-7680
Sarah WatsonINSERM U830, Diversity and Plasticity of Childhood Tumors Lab, PSL Research University, Institut Curie Research Center, Paris, France. sarah.watson@curie.fr.ORCID 0000-0003-4534-8783

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-EQPX-03Fondation ARC pour la Recherche sur le Cancer (ARC Foundation for Cancer Research) ARCPJA2021060004026
6 · The paper itself

Abstract

Dedifferentiated liposarcoma (DDLPS) is the most frequent high-grade soft tissue sarcoma subtype. It is characterized by a component of undifferentiated tumor cells coexisting with a component of well-differentiated adipocytic tumor cells. Both dedifferentiated (DD) and well-differentiated (WD) components exhibit MDM2 amplification, however their cellular origin remains elusive. Using single-cell RNA sequencing, DNA sequencing, in situ multiplex immunofluorescence and functional assays in paired WD and DD components from primary DDLPS tumors, we characterize the cellular heterogeneity of DDLPS tumor and micro-environment. We identify a population of tumor adipocyte stem cells (ASC) showing striking similarities with adipocyte stromal progenitors found in white adipose tissue. We show that tumor ASC harbor the ancestral genomic alterations of WD and DD components, suggesting that both derive from these progenitors following clonal evolution. Last, we show that DD tumor cells keep important biological properties of ASC including pluripotency and that their adipogenic properties are inhibited by a TGF-β-high immunosuppressive tumor micro-environment.

Indexed as

AdipocytesClonal EvolutionLiposarcomaProto-Oncogene Proteins c-mdm2Tumor MicroenvironmentAgedCell DedifferentiationCell DifferentiationFemaleHumansMaleMiddle AgedNeoplastic Stem CellsSingle-Cell AnalysisTransforming Growth Factor betaMDM2 protein, humanProto-Oncogene Proteins c-mdm2Transforming Growth Factor beta

Identifiers

PMID39266532
PMCPMC11393420

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.