CD44 and MMP14 Expression Associated with WHO Grade of the Astrocytoma and the Prognostic Implications.
- Author:
Jaekyung MYUNG
1
;
Bogun JANG
;
Heae Surng PARK
;
Woongjae YON
;
Hyun Ju LEE
;
Sung Hye PARK
Author Information
1. Department of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea. shparknp@snu.ac.kr
- Publication Type:Original Article
- Keywords:
Astrocytoma;
Antigens, CD44;
Matrix metalloproteinase 14;
Prognosis
- MeSH:
Antigens, CD44;
Astrocytoma;
Brain;
Breast;
Colon;
Disease Progression;
Female;
Humans;
Lung;
Matrix Metalloproteinase 14;
Multivariate Analysis;
Neoplasm Metastasis;
Ovary;
Prognosis;
Retrospective Studies;
World Health Organization
- From:Korean Journal of Pathology
2010;44(1):35-41
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: CD44 is a cell surface receptor that has been implicated in tumor cell invasion and metastasis in a range of tumors of various organs, including breast, ovary, colon, lung, and brain. CD44 stimulates the invasive ability by interacting with matrix metalloproteinase 14 (MMP14). The expression of MMP14 on the cell surface is thought to trigger multiple proteinase cascades and to stimulate cell migration. METHODS: A total 54 astrocytoma patients were eligible for this study. We performed a retrospective clinicopathological review and CD44 and MMP14 immunohistochemistry. RESULTS: The expressions of CD44 and MMP14 were significantly correlated with the World Health Organization (WHO) grade. On univariate analysis, the WHO grade and the expression of CD44 were the significant prognostic factors affecting overall survival (OS) and disease progression free survival (DPFS). On the multivariate analysis by the Cox regression model, the only WHO grade was shown to be a significant independent prognostic factor for predicting the DPFS and OS. CONCLUSIONS: In this study, the CD44 and MMP14 expressions were related to the WHO grade of astrocytoma. The CD44 expression status was a prognostic factor for DPFS and OS on univariate analysis, but it was not an independent prognostic factor on the multivariate analysis.
