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Neural precursor cell-expressed developmentally down-regulated 4-like: a new biomarker in the pathophysiology of endometrial cancer
OBJECTIVES: Endometrial cancer is the most frequent tumor of the female genital tract. Ubiquitin is a small protein (8.5 kDa) found in all eukaryotic cells, binds to substrate proteins via a three-phase enzymatic pathway referred to as ubiquitination and plays an important role in cellular stability...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136009/ https://www.ncbi.nlm.nih.gov/pubmed/29998764 http://dx.doi.org/10.1177/0300060518777944 |
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author | Yilmaz, Ercan Gul, Mehmet Melekoglu, Rauf Inci Coskun, Ebru Sahin, Nurhan Gul, Semir Bastemur, Ayse Gulcin Ciplak, Baris |
author_facet | Yilmaz, Ercan Gul, Mehmet Melekoglu, Rauf Inci Coskun, Ebru Sahin, Nurhan Gul, Semir Bastemur, Ayse Gulcin Ciplak, Baris |
author_sort | Yilmaz, Ercan |
collection | PubMed |
description | OBJECTIVES: Endometrial cancer is the most frequent tumor of the female genital tract. Ubiquitin is a small protein (8.5 kDa) found in all eukaryotic cells, binds to substrate proteins via a three-phase enzymatic pathway referred to as ubiquitination and plays an important role in cellular stability. Neural precursor cell-expressed developmentally down-regulated 4-like (NEDD4L) functions in the last phase of this enzymatic process. In this study, we investigated NEDD4L protein expression in endometrial cancer. METHODS: The study participants were divided into patients with benign endometrial pathologies (Group 1, n = 23), patients with endometrial hyperplasia (Group 2, n = 21) and patients with endometrial cancer (Group 3, n = 20). NEDD4L expression was detected by immunohistochemical staining and H scores were calculated to standardize staining intensity. Statistical analysis was performed using SPSS 16.0. RESULTS: NEDD4L expression levels according to H scores were significantly lower in patients diagnosed with endometrial cancer compared with those with benign endometrial pathologies. CONCLUSION: NEDD4L is involved in maintaining cell stability, and reduced NEDD4L expression as a result of gene mutation may disrupt this balance in favor of tumorigenesis. |
format | Online Article Text |
id | pubmed-6136009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61360092018-09-17 Neural precursor cell-expressed developmentally down-regulated 4-like: a new biomarker in the pathophysiology of endometrial cancer Yilmaz, Ercan Gul, Mehmet Melekoglu, Rauf Inci Coskun, Ebru Sahin, Nurhan Gul, Semir Bastemur, Ayse Gulcin Ciplak, Baris J Int Med Res Clinical Research Reports OBJECTIVES: Endometrial cancer is the most frequent tumor of the female genital tract. Ubiquitin is a small protein (8.5 kDa) found in all eukaryotic cells, binds to substrate proteins via a three-phase enzymatic pathway referred to as ubiquitination and plays an important role in cellular stability. Neural precursor cell-expressed developmentally down-regulated 4-like (NEDD4L) functions in the last phase of this enzymatic process. In this study, we investigated NEDD4L protein expression in endometrial cancer. METHODS: The study participants were divided into patients with benign endometrial pathologies (Group 1, n = 23), patients with endometrial hyperplasia (Group 2, n = 21) and patients with endometrial cancer (Group 3, n = 20). NEDD4L expression was detected by immunohistochemical staining and H scores were calculated to standardize staining intensity. Statistical analysis was performed using SPSS 16.0. RESULTS: NEDD4L expression levels according to H scores were significantly lower in patients diagnosed with endometrial cancer compared with those with benign endometrial pathologies. CONCLUSION: NEDD4L is involved in maintaining cell stability, and reduced NEDD4L expression as a result of gene mutation may disrupt this balance in favor of tumorigenesis. SAGE Publications 2018-07-12 2018-09 /pmc/articles/PMC6136009/ /pubmed/29998764 http://dx.doi.org/10.1177/0300060518777944 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Research Reports Yilmaz, Ercan Gul, Mehmet Melekoglu, Rauf Inci Coskun, Ebru Sahin, Nurhan Gul, Semir Bastemur, Ayse Gulcin Ciplak, Baris Neural precursor cell-expressed developmentally down-regulated 4-like: a new biomarker in the pathophysiology of endometrial cancer |
title | Neural precursor cell-expressed developmentally down-regulated
4-like: a new biomarker in the pathophysiology of endometrial
cancer |
title_full | Neural precursor cell-expressed developmentally down-regulated
4-like: a new biomarker in the pathophysiology of endometrial
cancer |
title_fullStr | Neural precursor cell-expressed developmentally down-regulated
4-like: a new biomarker in the pathophysiology of endometrial
cancer |
title_full_unstemmed | Neural precursor cell-expressed developmentally down-regulated
4-like: a new biomarker in the pathophysiology of endometrial
cancer |
title_short | Neural precursor cell-expressed developmentally down-regulated
4-like: a new biomarker in the pathophysiology of endometrial
cancer |
title_sort | neural precursor cell-expressed developmentally down-regulated
4-like: a new biomarker in the pathophysiology of endometrial
cancer |
topic | Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136009/ https://www.ncbi.nlm.nih.gov/pubmed/29998764 http://dx.doi.org/10.1177/0300060518777944 |
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