| Makale Türü |
|
| Makale Alt Türü | SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale |
| Dergi Adı | Journal of International Medicak Research |
| Dergi ISSN | 0300-0605 Wos Dergi Scopus Dergi |
| Dergi Tarandığı Indeksler | SCI-Expanded |
| Dergi Grubu | Q4 |
| Makale Dili | İngilizce |
| Basım Tarihi | 09-2018 |
| Cilt No | 46 |
| Sayı | 9 |
| Sayfalar | 3709 / 3716 |
| DOI Numarası | 10.1177/0300060518777944 |
| Özet |
| 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. |
| Anahtar Kelimeler |
| NEDD4L | endometrial cancer | ubiquitin | tumorigenesis | endometrial hyperplasia | immunohistochemistry |
| Dergi Adı | JOURNAL OF INTERNATIONAL MEDICAL RESEARCH |
| Yayıncı | SAGE Publications Ltd |
| Açık Erişim | Evet |
| ISSN | 0300-0605 |
| E-ISSN | 1473-2300 |
| CiteScore | 3,1 |
| SJR | 0,474 |
| SNIP | 0,722 |