The association of miR-204 and mir-483 5p expression with clinicopathological features of Wilms tumor: Could this provide foresight?
Özet
Background: Wilms tumor is the most common cancer of the kidney that occurs during childhood, and histologically, it mimics renal embryogenesis. With the development and improvement of up-to-date treatment protocols, the survival rates of Wilms tumor have increased. However, metastases or local relapses are still observed in 15% of patients. The search for reliable biomarkers to identify at-risk patients is ongoing to predict the variability in treatment success. Currently, the evaluation of clinical, histopathological and genetic features are common diagnostic methods; however, epigenetic features can be examined with microRNA expression analyses and might allow us to comment on the behavior of the tumor and treatment response. Methods: In this study, we aimed to evaluate the relationship between microRNA-204 and microRNA-483-5p expression with clinicopathological data and the effect on Wilms tumor survival. For this purpose, the expression levels of RNU6B, microRNA-204 and microRNA-483-5p were evaluated in tumor and normal tissue by qreal time-polymerase chain reaction. We also investigated the relationship between microRNA expression levels with the clinicopathological and histological features of Wilms tumor. Results and conclusion: The results of our study indicate that the relative expression levels of microRNA-204 in Wilms tumor tissues were significantly lower than that in adjacent normal tissues. By contrast, tumor tissue had a higher microRNA-483-5p expression than the corresponding normal tissues. A statistically significant difference between microRNA-204 expression level with age and the presence of anaplasia was observed. The upregulation of microRNA-483-5p was found to have a significant correlation with patients after preoperative chemotherapy and complete tumor necrosis. Taken together, our data suggest that microRNA-204 could play a critical role as a tumor suppressor, whereas microRNA-483-5p acts as an oncogene in Wilms tumor progression. More importantly, microRNA-204 might be a novel predictive biomarker for anaplastic histology and could be useful for developing therapeutic interventions targeting this marker. © The Author(s) 2023. Published by Oxford University Press. All rights reserved.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Calli, Aylin Orgen | |
| dc.contributor.author | Issin, Gizem | |
| dc.contributor.author | Yilmaz, Ismail | |
| dc.contributor.author | Ince, Dilek | |
| dc.contributor.author | Tural, Ersin | |
| dc.contributor.author | Guzelis, Ismail | |
| dc.contributor.author | Cecen, Refik Emre | |
| dc.contributor.author | Olgun, Hatice Nur | |
| dc.contributor.author | Gokcay, Deniz | |
| dc.contributor.author | Ozer, Erdener | |
| dc.date.accessioned | 2026-10-18T20:26:43.434663768Z | |
| dc.date.available | 2026-10-18T20:26:43.434663768Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Background: Wilms tumor is the most common cancer of the kidney that occurs during childhood, and histologically, it mimics renal embryogenesis. With the development and improvement of up-to-date treatment protocols, the survival rates of Wilms tumor have increased. However, metastases or local relapses are still observed in 15% of patients. The search for reliable biomarkers to identify at-risk patients is ongoing to predict the variability in treatment success. Currently, the evaluation of clinical, histopathological and genetic features are common diagnostic methods; however, epigenetic features can be examined with microRNA expression analyses and might allow us to comment on the behavior of the tumor and treatment response. Methods: In this study, we aimed to evaluate the relationship between microRNA-204 and microRNA-483-5p expression with clinicopathological data and the effect on Wilms tumor survival. For this purpose, the expression levels of RNU6B, microRNA-204 and microRNA-483-5p were evaluated in tumor and normal tissue by qreal time-polymerase chain reaction. We also investigated the relationship between microRNA expression levels with the clinicopathological and histological features of Wilms tumor. Results and conclusion: The results of our study indicate that the relative expression levels of microRNA-204 in Wilms tumor tissues were significantly lower than that in adjacent normal tissues. By contrast, tumor tissue had a higher microRNA-483-5p expression than the corresponding normal tissues. A statistically significant difference between microRNA-204 expression level with age and the presence of anaplasia was observed. The upregulation of microRNA-483-5p was found to have a significant correlation with patients after preoperative chemotherapy and complete tumor necrosis. Taken together, our data suggest that microRNA-204 could play a critical role as a tumor suppressor, whereas microRNA-483-5p acts as an oncogene in Wilms tumor progression. More importantly, microRNA-204 might be a novel predictive biomarker for anaplastic histology and could be useful for developing therapeutic interventions targeting this marker. © The Author(s) 2023. Published by Oxford University Press. All rights reserved. | |
| dc.identifier.doi | 10.1093/jjco/hyad113 | |
| dc.identifier.eissn | 1465-3621 | |
| dc.identifier.endpage | 1176 | |
| dc.identifier.issn | 0368-2811 | |
| dc.identifier.issue | 12 | |
| dc.identifier.pmid | 37647636 | |
| dc.identifier.scopus | 2-s2.0-85179134423 | |
| dc.identifier.startpage | 1170 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/11716 | |
| dc.identifier.volume | 53 | |
| dc.identifier.wos | WOS:001062104400001 | |
| dc.language.iso | en | |
| dc.publisher | Oxford University Press | |
| dc.relation.ispartof | Japanese Journal of Clinical Oncology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | micro-RNA | |
| dc.subject | miR-204 | |
| dc.subject | miR-483-5p | |
| dc.subject | Wilms tumor | |
| dc.subject | Cell Proliferation | |
| dc.subject | Gene Expression Regulation, Neoplastic | |
| dc.subject | Humans | |
| dc.subject | Kidney Neoplasms | |
| dc.subject | MicroRNAs | |
| dc.subject | Neoplasm Recurrence, Local | |
| dc.subject | Up-Regulation | |
| dc.subject | biological marker | |
| dc.subject | microRNA | |
| dc.subject | microRNA 204 | |
| dc.subject | microRNA 483 5p | |
| dc.subject | unclassified drug | |
| dc.subject | MIRN204 microRNA, human | |
| dc.subject | MIRN483 microRNA, human | |
| dc.subject | adolescent | |
| dc.subject | adult | |
| dc.subject | Article | |
| dc.subject | cancer staging | |
| dc.subject | cancer survival | |
| dc.subject | child | |
| dc.subject | controlled study | |
| dc.subject | down regulation | |
| dc.subject | embryo | |
| dc.subject | embryo development | |
| dc.subject | epigenetics | |
| dc.subject | epithelial mesenchymal transition | |
| dc.title | The association of miR-204 and mir-483 5p expression with clinicopathological features of Wilms tumor: Could this provide foresight? | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 2 | |
| rdl.citation.wos | 2 | |
| rdl.department | Department of Pathology, Mengucek Gazi Training and Research Hospital, Erzincan Binali Yıldırım University, Erzincan, Turkiye. | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
