Stromal Clues in Endometrial Carcinoma: Loss of Expression of β-Catenin, Epithelial-Mesenchymal Transition Regulators, and Estrogen-Progesterone Receptor. (May 2016)
- Record Type:
- Journal Article
- Title:
- Stromal Clues in Endometrial Carcinoma: Loss of Expression of β-Catenin, Epithelial-Mesenchymal Transition Regulators, and Estrogen-Progesterone Receptor. (May 2016)
- Main Title:
- Stromal Clues in Endometrial Carcinoma
- Authors:
- Senol, Serkan
Sayar, Ilyas
Ceyran, Ayse B.
Ibiloglu, Ibrahim
Akalin, Ibrahim
Firat, Ugur
Kosemetin, Duygu
Engin Zerk, Pinar
Aydin, Abdullah - Abstract:
- Abstract : Epithelial-stroma interactions in the endometrium are known to be responsible for physiological functions and emergence of several pathologic lesions. Periglandular stromal cells act on endometrial cells in a paracrine manner through sex hormones. In this study, we immunohistochemically evaluated the expression of epithelial-mesenchymal transition regulators (SNAIL/SLUG, TWIST, ZEB1), adhesion molecules (β-catenin and E-cadhenin), estrogen (ER)-progesterone (PR) receptor and their correlation with each other in 30 benign, 148 hyperplastic (EH), and 101 endometrioid-type endometrial carcinoma (EC) endometria. In the epithelial component, loss of expression in E-cadherin, ER and PR, and overexpression of TWIST and ZEB1 were significantly higher in EC than in EH ( P <0.01). In the periglandular stromal component, β-catenin and SNAIL/SLUG expression were significantly higher in normal endometrium and simple without atypical EH compared with complex atypical EH and EC ( P <0.01). In addition, periglandular stromal TWIST expression was significantly higher in EH group compared with EC ( P <0.05). There was significantly negative correlation between β-catenin and ER, TWIST and ER, and TWIST and PR in hyperplastic and carcinomatous glandular epithelium, whereas there was a significantly positive correlation between β-catenin and SNAIL-SLUG, β-catenin and TWIST, β-catenin and ER, β-catenin and PR, SNAIL-SLUG and ER, SNAIL-SLUG and PR, TWIST and ER, TWIST and PR, inAbstract : Epithelial-stroma interactions in the endometrium are known to be responsible for physiological functions and emergence of several pathologic lesions. Periglandular stromal cells act on endometrial cells in a paracrine manner through sex hormones. In this study, we immunohistochemically evaluated the expression of epithelial-mesenchymal transition regulators (SNAIL/SLUG, TWIST, ZEB1), adhesion molecules (β-catenin and E-cadhenin), estrogen (ER)-progesterone (PR) receptor and their correlation with each other in 30 benign, 148 hyperplastic (EH), and 101 endometrioid-type endometrial carcinoma (EC) endometria. In the epithelial component, loss of expression in E-cadherin, ER and PR, and overexpression of TWIST and ZEB1 were significantly higher in EC than in EH ( P <0.01). In the periglandular stromal component, β-catenin and SNAIL/SLUG expression were significantly higher in normal endometrium and simple without atypical EH compared with complex atypical EH and EC ( P <0.01). In addition, periglandular stromal TWIST expression was significantly higher in EH group compared with EC ( P <0.05). There was significantly negative correlation between β-catenin and ER, TWIST and ER, and TWIST and PR in hyperplastic and carcinomatous glandular epithelium, whereas there was a significantly positive correlation between β-catenin and SNAIL-SLUG, β-catenin and TWIST, β-catenin and ER, β-catenin and PR, SNAIL-SLUG and ER, SNAIL-SLUG and PR, TWIST and ER, TWIST and PR, in periglandular/cancer-associated stromal cells ( P <0.01). In conclusion, the pattern of positive and negative correlations in the expression of epithelial-mesenchymal transition regulators (SNAIL-SLUG and TWIST), sex hormone receptors (ER and PR), and β-catenin between ECs and hyperplasia, as well as between epithelium and stroma herein, is suggestive of a significant role for these proteins and their underlying molecular processes in the development of endometrial carcinomas. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- International journal of gynecological pathology. Volume 35:Number 3(2016)
- Journal:
- International journal of gynecological pathology
- Issue:
- Volume 35:Number 3(2016)
- Issue Display:
- Volume 35, Issue 3 (2016)
- Year:
- 2016
- Volume:
- 35
- Issue:
- 3
- Issue Sort Value:
- 2016-0035-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-05
- Subjects:
- Endometrium -- EMT -- β-Catenin -- E-cadherin -- Sex steroid receptors
Gynecologic pathology -- Periodicals
Gynecology -- Periodicals
Generative organs, Female -- Diseases -- Periodicals
618.10705 - Journal URLs:
- http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00004347-000000000-00000 ↗
http://www.intjgynpathology.com ↗
http://journals.lww.com/intjgynpathology/pages/currenttoc.aspx ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/PGP.0000000000000233 ↗
- Languages:
- English
- ISSNs:
- 0277-1691
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.274000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5220.xml