Abstract |
The purpose of this study was to determine the expression and potential clinical role of epithelial-to-mesenchymal transition (EMT)-related factors in malignant ovarian germ cell tumors (MOGCT). Protein expression of E-cadherin, N-cadherin, P-cadherin, Zeb1, HMGA2, and vimentin by immunohistochemistry was analyzed in 42 MOGCT from patients treated in Norway during the period 1981-2001. Expression was analyzed for association with clinicopathologic parameters. E-cadherin (p = 0.016) and HMGA2 (p = 0.002) expression was significantly higher in immature teratomas and yolk sac tumors compared with dysgerminomas. Vimentin (p < 0.001) and Zeb1 (p = 0.029) staining was significantly higher in immature teratomas compared with yolk sac tumors and dysgerminomas, whereas no significant differences were observed for N-cadherin and P-cadherin. EMT-associated markers were not significantly related to clinicopathologic parameters including age, tumor diameter, and FIGO stage. In conclusion, based on this limited series, EMT-associated markers are not associated with clinical parameters in MOGCT, in contrast to ovarian carcinoma. EMT-related proteins are differentially expressed among various MOGCT subtypes, suggesting differences in biological characteristics associated with invasion and metastasis.
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Authors | Olesya Solheim, Mette Førsund, Claes G Tropé, Sigrid Marie Kraggerud, Jahn M Nesland, Ben Davidson |
Journal | APMIS : acta pathologica, microbiologica, et immunologica Scandinavica
(APMIS)
Vol. 125
Issue 9
Pg. 781-786
(Sep 2017)
ISSN: 1600-0463 [Electronic] Denmark |
PMID | 28585395
(Publication Type: Journal Article)
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Copyright | © 2017 APMIS. Published by John Wiley & Sons Ltd. |
Chemical References |
- Biomarkers, Tumor
- Cadherins
- HMGA2 Protein
- Vimentin
- ZEB1 protein, human
- Zinc Finger E-box-Binding Homeobox 1
|
Topics |
- Adolescent
- Adult
- Biomarkers, Tumor
(metabolism)
- Cadherins
(metabolism)
- Child
- Dysgerminoma
(pathology)
- Epithelial-Mesenchymal Transition
(physiology)
- Female
- HMGA2 Protein
(metabolism)
- Humans
- Immunohistochemistry
- Middle Aged
- Neoplasms, Germ Cell and Embryonal
(pathology, therapy)
- Ovarian Neoplasms
(pathology, therapy)
- Teratoma
(pathology)
- Vimentin
(metabolism)
- Young Adult
- Zinc Finger E-box-Binding Homeobox 1
(metabolism)
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