Are micro-RNA 21 and 143 indicative as prognostic biomarkers in dedifferentiated endometrial adenocarcinoma?

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Aim: Dedifferentiated endometrial adenocarcinoma (DEAC) is a rare, aggressive subtype, accounting for 2% of all endometrial cancers. Poor survival in DEAC prompts the need for effective treatment modalities through better prognostic classification. MicroRNAs (miRNA) have essential roles in tumor angiogenesis, which might enable their use as novel biomarkers. In this study, we aimed to reveal the relationship between the expression of miRNA-21 and miRNA-143, which are associated with angiogenesis, and the prognosis of DEAC. Method: The study included six cases diagnosed with DEAC. The expression levels of miRNA-21 and miRNA-143 were detected by quantitative real-time PCR. Microvascular density (MVD) was measured by CD34 staining. All data and effects on survival were compared for statistical significance. Results: Six cases diagnosed with DEAC were included in the study. The percentage of undifferentiated components ranged from 50 to 90%. The second component of differentiated carcinoma was detected as endometrioid (3/5 grade I, 1/5 grade II, 1/5 grade III) in five cases and serous in one case. The mean MVD was 27 (range 17–44, SD 9.4). In three cases, miRNA-21 expression was down-regulated in neoplastic areas compared to non-neoplastic areas. On the contrary, it was found to be up-regulated in the remaining three cases. MiRNA-143 expression decreased in four cases and increased in two cases. Conclusions: Based on these findings, we found a significant irregular expression of miRNA-21 in DEACs. As in other cancers, angiogenesis is significantly associated with survival in DEACs. This study provides initial data for revealing possible implications of miRNAs as prognostic indicators in DEAC. © The Author(s), under exclusive licence to Springer Nature B.V. 2024.

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https://rdlopen.rawdatalibrary.net/r/ebyu/11452Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s11033-024-09663-7Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorCalli, Aylin Orgen
dc.contributor.authorKurt, Kerem
dc.contributor.authorNarli, Gizem
dc.contributor.authorKocabey, Duygu Unal
dc.contributor.authorYilmaz, Alpay
dc.contributor.authorOcal, Irfan
dc.contributor.authorYigit, Seyran
dc.contributor.authorYilmaz, Ismail
dc.date.accessioned2026-10-18T20:26:29.768055227Z
dc.date.available2026-10-18T20:26:29.768055227Z
dc.date.issued2024
dc.description.abstractAim: Dedifferentiated endometrial adenocarcinoma (DEAC) is a rare, aggressive subtype, accounting for 2% of all endometrial cancers. Poor survival in DEAC prompts the need for effective treatment modalities through better prognostic classification. MicroRNAs (miRNA) have essential roles in tumor angiogenesis, which might enable their use as novel biomarkers. In this study, we aimed to reveal the relationship between the expression of miRNA-21 and miRNA-143, which are associated with angiogenesis, and the prognosis of DEAC. Method: The study included six cases diagnosed with DEAC. The expression levels of miRNA-21 and miRNA-143 were detected by quantitative real-time PCR. Microvascular density (MVD) was measured by CD34 staining. All data and effects on survival were compared for statistical significance. Results: Six cases diagnosed with DEAC were included in the study. The percentage of undifferentiated components ranged from 50 to 90%. The second component of differentiated carcinoma was detected as endometrioid (3/5 grade I, 1/5 grade II, 1/5 grade III) in five cases and serous in one case. The mean MVD was 27 (range 17–44, SD 9.4). In three cases, miRNA-21 expression was down-regulated in neoplastic areas compared to non-neoplastic areas. On the contrary, it was found to be up-regulated in the remaining three cases. MiRNA-143 expression decreased in four cases and increased in two cases. Conclusions: Based on these findings, we found a significant irregular expression of miRNA-21 in DEACs. As in other cancers, angiogenesis is significantly associated with survival in DEACs. This study provides initial data for revealing possible implications of miRNAs as prognostic indicators in DEAC. © The Author(s), under exclusive licence to Springer Nature B.V. 2024.
dc.identifier.doi10.1007/s11033-024-09663-7
dc.identifier.eissn1573-4978
dc.identifier.issn0301-4851
dc.identifier.issue1
dc.identifier.pmid38874783
dc.identifier.scopus2-s2.0-85195913396
dc.identifier.startpage756
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11452
dc.identifier.volume51
dc.identifier.wosWOS:001249231800006
dc.language.isoen
dc.publisherSpringer Science and Business Media B.V.
dc.relation.ispartofMolecular Biology Reports
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCarcinoma
dc.subjectEndometrial neoplasms
dc.subjectMicroRNAs
dc.subjectPrognosis
dc.subjectAdenocarcinoma
dc.subjectAdult
dc.subjectAged
dc.subjectBiomarkers, Tumor
dc.subjectFemale
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectMiddle Aged
dc.subjectNeovascularization, Pathologic
dc.subjectbiological marker
dc.subjectCD34 antigen
dc.subjectmicroRNA 143
dc.subjectmicroRNA 21
dc.subjectmicroRNA
dc.subjectMIRN143 microRNA, human
dc.subjectMIRN21 microRNA, human
dc.subjecttumor marker
dc.subjectangiogenesis
dc.subjectArticle
dc.subjectcancer survival
dc.subjectclinical article
dc.subjectendometrium carcinoma
dc.subjectfollow up
dc.subjecthistology
dc.subjecthistopathology
dc.subjecthuman
dc.titleAre micro-RNA 21 and 143 indicative as prognostic biomarkers in dedifferentiated endometrial adenocarcinoma?
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.citation.wos0
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)