Evidence map›Paper›PMID 39368400›Full record

ArticleClinics (Sao Paulo, Brazil)2024

IMP3, CDK4, MDM2 and β-catenin expression in Enchondroma and Central Chondrosarcoma: Diagnostic and prognostic utility.

Daniele Moraes Losada, Maurício Etchebehere, Francisco Fontes Cintra, Eliane Maria Ingrid Amstalden

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Article in Clinics (Sao Paulo, Brazil), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Daniele Moraes LosadaDepartment of Pathology, Universidade Estatual de Campinas (Unicamp), Campinas, SP, Brazil. Electronic address: danielelosada@hotmail.com.
Maurício EtchebehereHospital de Clínicas da Universidade Estadual de Campinas (Unicamp), Campinas, SP, Brazil.
Francisco Fontes CintraHospital de Clínicas da Universidade Estadual de Campinas (Unicamp), Campinas, SP, Brazil.
Eliane Maria Ingrid AmstaldenDepartment of Pathology, Universidade Estatual de Campinas (Unicamp), Campinas, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe role of IMP3, CDK4, MDM2 and β-catenin proteins in Enchondroma and Central Chondrosarcoma is not totally understood. The aim of this study is to evaluate the immunoexpression of these proteins, associating histological grade, clinical data and prognosis to these tumors.

methodsThis is a retrospective-analytical study of 32 Enchondroma and 70 Central Chondrosarcoma.

resultsIMP3, CDK4, MDM2 and β-catenin expression was observed in 22.82 %, 13.82 %, 17.17 % and in 8.8 % of cases, respectively. All Enchondromas positive for these immunomarkers were located in short tubular bones. The positivity for these antibodies is directly proportional to Chondrosarcoma's histological grade increase. No difference was found between Enchondroma and Chondrosarcoma, Grade 1 for IMP3, CDK4 and ß-catenin positivity. Significant metastasis outcome was observed for IMP3, CDK4, MDM2 and death for MDM2 expression.

conclusionIMP3, CDK4, MDM2 and β-catenin expression in Enchondromas of short bones phenotypically characterizes these tumors. Their expression has not proven to be useful either as diagnostic markers of these neoplasms or in distinguishing between Enchondroma and Chondrosarcoma, Grade 1. The significant immunoexpression of IMP3, CDK4 and MDM2 in metastatic Chondrosarcoma and the lower survival in those with positivity for MDM2 suggest a possible association of these proteins with tumor aggressiveness.

Indexed as

beta CateninBiomarkers, TumorBone NeoplasmsChondromaChondrosarcomaCyclin-Dependent Kinase 4ImmunohistochemistryProto-Oncogene Proteins c-mdm2AdolescentAdultAgedChildFemaleHumansMaleMiddle Agedbeta CateninBiomarkers, TumorCyclin-Dependent Kinase 4IGF2BP3 protein, humanMDM2 protein, humanProto-Oncogene Proteins c-mdm2RNA-Binding ProteinsBeta cateninChondromaChondrosarcomaCyclic IMPCyclin-dependent kinase 4ImmunohistochemistryProto-oncogene proteins c-mdm2

Identifiers

PMID39368400
PMCPMC11490761

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