Evidence map›Paper›PMID 41257933›Full record

ArticleScientific reports2025

Molecular profiling of endometrial cancer in Martinique reveals frequent CCNE1 amplification in poor prognosis tumors.

Taina Labeau, Jean-Samuel Loger, Mehdi Jean-Laurent, Quentin Hurlot, Cloé Jean-Laurent, Ludivine Chevallier, Sabrina Pennont, Sarah Lise, Sarah Amari, Judicaelle Montlouis-Calixte and 5 more

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

  1. Feasibility ofCancers · 2026
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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Taina LabeauDepartment of Gynecological and Breast Surgery, University Hospital of Martinique, Martinique, France.
Jean-Samuel LogerDepartment of Cancer Molecular Genetics, University Hospital of Martinique, Martinique, France.
Mehdi Jean-LaurentDepartment of Gynecological and Breast Surgery, University Hospital of Martinique, Martinique, France.
Quentin HurlotDepartment of Pathology, University Hospital of Martinique, Martinique, France.
Cloé Jean-LaurentDepartment of Cancer Molecular Genetics, University Hospital of Martinique, Martinique, France.
Ludivine ChevallierDepartment of Gynecological and Breast Surgery, University Hospital of Martinique, Martinique, France.
Sabrina PennontDepartment of Cancer Molecular Genetics, University Hospital of Martinique, Martinique, France.
Sarah LiseDepartment of Gynecological and Breast Surgery, University Hospital of Martinique, Martinique, France.
Sarah AmariDepartment of Gynecological and Breast Surgery, University Hospital of Martinique, Martinique, France.
Judicaelle Montlouis-CalixteDepartment of Gynecological and Breast Surgery, University Hospital of Martinique, Martinique, France.
Odile BéraDepartment of Cancer Molecular Genetics, University Hospital of Martinique, Martinique, France.
Alexis VallardMartinique Regional Oncology Platform, University Hospital of Martinique, Martinique, France.
Heriniaina RandriamiarisoaDepartment of Pathology, University Hospital of Martinique, Martinique, France.
Emeline ColombaDepartment of Cancer Medicine, Institut Gustave Roussy, University of Paris Saclay, Paris, France.
Régine MarlinDepartment of Cancer Molecular Genetics, University Hospital of Martinique, Martinique, France. Regine.marlin@chu-martinique.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn Martinique, there is an unmet need in EC management. Although the incidence rate is similar to that in mainland France, the mortality rate is higher, potentially due to the over-incidence of high-grade tumors. Recently, we reported CCNE1 amplification in 70% of these tumors which have a poor prognosis. This alteration has been observed in non-endometrioid subtypes of African American women. To elucidate the over-incidence of poor prognosis EC in Martinique, we aim to describe molecular profiles especially CCNE1 amplification of a cohort of all patient diagnosed between January 2023 and June 2024.

methodsCCNE1 amplification status was determined using digital PCR. We also performed the analysis of POLE, MMR and TP53 to classified tumors in current molecular classification. A total of 55 patients were included in our study, revealing a different distribution of biomarkers than described in the literature.

resultsWe reported an over-incidence of TP53 mutations and CCNE1 amplification. Conversely, the prevalence of POLE mutations was lower. In this study, non-endometrioid subtypes were particularly associated with CCNE1 amplification that is consistent with previous studies. The molecular classification observed in our cohort is consistent with findings in populations of African descent. The higher CCNE1 amplification rate mirrors those seen in these populations.

conclusionGiven the ethnic origin of the Martinique population, these data suggest that CCNE1 amplification may be linked to African genetic heritage and could explain the over-incidence of non-endometrioid subtypes in these populations. Furthermore, our study contributes to addressing racial disparities in endometrial cancer outcomes by providing crucial insights into the genetic factors that may influence the prognosis of African-descended populations.

Indexed as

Cyclin EEndometrial NeoplasmsGene AmplificationOncogene ProteinsAdultAgedBiomarkers, TumorFemaleHumansMartiniqueMiddle AgedMutationPrognosisTumor Suppressor Protein p53Biomarkers, TumorCCNE1 protein, humanCyclin EOncogene ProteinsTumor Suppressor Protein p53African descentCCNE1 amplificationEndometrial cancerEthnic disparities

Identifiers

PMID41257933
PMCPMC12630616

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