Are micro-RNA 21 and 143 indicative as prognostic biomarkers in dedifferentiated endometrial adenocarcinoma?
Özet
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.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Calli, Aylin Orgen | |
| dc.contributor.author | Kurt, Kerem | |
| dc.contributor.author | Narli, Gizem | |
| dc.contributor.author | Kocabey, Duygu Unal | |
| dc.contributor.author | Yilmaz, Alpay | |
| dc.contributor.author | Ocal, Irfan | |
| dc.contributor.author | Yigit, Seyran | |
| dc.contributor.author | Yilmaz, Ismail | |
| dc.date.accessioned | 2026-10-18T20:26:29.768055227Z | |
| dc.date.available | 2026-10-18T20:26:29.768055227Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | 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. | |
| dc.identifier.doi | 10.1007/s11033-024-09663-7 | |
| dc.identifier.eissn | 1573-4978 | |
| dc.identifier.issn | 0301-4851 | |
| dc.identifier.issue | 1 | |
| dc.identifier.pmid | 38874783 | |
| dc.identifier.scopus | 2-s2.0-85195913396 | |
| dc.identifier.startpage | 756 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/11452 | |
| dc.identifier.volume | 51 | |
| dc.identifier.wos | WOS:001249231800006 | |
| dc.language.iso | en | |
| dc.publisher | Springer Science and Business Media B.V. | |
| dc.relation.ispartof | Molecular Biology Reports | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Carcinoma | |
| dc.subject | Endometrial neoplasms | |
| dc.subject | MicroRNAs | |
| dc.subject | Prognosis | |
| dc.subject | Adenocarcinoma | |
| dc.subject | Adult | |
| dc.subject | Aged | |
| dc.subject | Biomarkers, Tumor | |
| dc.subject | Female | |
| dc.subject | Gene Expression Regulation, Neoplastic | |
| dc.subject | Humans | |
| dc.subject | Middle Aged | |
| dc.subject | Neovascularization, Pathologic | |
| dc.subject | biological marker | |
| dc.subject | CD34 antigen | |
| dc.subject | microRNA 143 | |
| dc.subject | microRNA 21 | |
| dc.subject | microRNA | |
| dc.subject | MIRN143 microRNA, human | |
| dc.subject | MIRN21 microRNA, human | |
| dc.subject | tumor marker | |
| dc.subject | angiogenesis | |
| dc.subject | Article | |
| dc.subject | cancer survival | |
| dc.subject | clinical article | |
| dc.subject | endometrium carcinoma | |
| dc.subject | follow up | |
| dc.subject | histology | |
| dc.subject | histopathology | |
| dc.subject | human | |
| dc.title | Are micro-RNA 21 and 143 indicative as prognostic biomarkers in dedifferentiated endometrial adenocarcinoma? | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 0 | |
| rdl.citation.wos | 0 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
