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MMP-14 and CD44 in Epithelial-to-Mesenchymal Transition (EMT) in ovarian cancer.

Authors :
Vos MC
Hollemans E
Ezendam N
Feijen H
Boll D
Pijlman B
van der Putten H
Klinkhamer P
van Kuppevelt TH
van der Wurff AA
Massuger LF
Source :
Journal of ovarian research [J Ovarian Res] 2016 Sep 02; Vol. 9 (1), pp. 53. Date of Electronic Publication: 2016 Sep 02.
Publication Year :
2016

Abstract

Background: To investigate the expression of MMP-14 and CD44 as well as epithelial-to-mesenchymal transition(EMT)-like changes in ovarian cancer and to determine correlations with clinical outcome.<br />Methods: In 97 patients with ovarian cancer, MMP-14 and CD44 expression as determined by immunohistochemistry was investigated in relation to EMT-like changes. To determine this, immunohistochemical staining of E-cadherin and vimentin was performed.<br />Results: Patients with expression of both MMP-14 and CD44 in their tumors had a poor prognosis despite complete debulking. Serous histology in advanced-stage tumors (FIGO IIB-IV) correlated with CD44 (rho .286, p < 0.01). Also, CD44 correlated with percentage vimentin expression (rho .217, p < 0.05). In logistic regression analysis with complete debulking as the outcome parameter, CD44 expression was found to be significant (OR 3,571 (95 % Confidence Interval 1,112-11,468) p = 0.032), though this was not the case for MMP-14 and EMT parameters.<br />Conclusion: The subgroup of patients with double expression of MMP-14 and CD44 had a poor prognosis despite complete debulking. Serous subtype in advanced-stage patients and CD44 expression were found to be correlated with vimentin expression, and CD44 expression was found to be significantly correlated with complete debulking. However, a significant correlation between EMT and clinical parameters was not found.

Details

Language :
English
ISSN :
1757-2215
Volume :
9
Issue :
1
Database :
MEDLINE
Journal :
Journal of ovarian research
Publication Type :
Academic Journal
Accession number :
27590006
Full Text :
https://doi.org/10.1186/s13048-016-0262-7