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Aberrant expression of beta-catenin, Pin1 and cylin D1 in salivary adenoid cystic carcinoma: relation to tumor proliferation and metastasis.
- Source :
-
Oncology reports [Oncol Rep] 2006 Sep; Vol. 16 (3), pp. 505-11. - Publication Year :
- 2006
-
Abstract
- The aims of this study were to investigate the expression levels of beta-catenin, Pin1 and cyclin D1 in salivary adenoid cystic carcinomas (SACC ) and to evaluate its clinical importance, furthermore, to elucidate whether beta-catenin expression was aberrant in SACC and whether Pin1 was involved in aberrant beta-catenin and cyclin D1 expression. The expression of Pin1, beta-catenin and cyclin D1 were examined in the specimens of 65 patients with SACC by immunohistochemistry, protein and mRNA expressions were detected by western blotting and RT-PCR in four SACC cell lines. Pin1 was overexpressed in 51 cases of SACC (78%), and high levels of Pin1 expression correlated with cyclin D1 positive expression (p = 0.02). Fourteen (22%) cases showed positive immunoreactivity for beta-catenin protein in the nuclear/cytoplasmic fraction in tumor tissues, which was defined as cytoplasm/nucleus staining, among which quite evident nuclear expression of beta-catenin was detected in six cases (9%), while cyclin D1 positive expression was detected in 41 cases of SACC (63%). Reduced membranous expression of beta-catenin was detected in the cases with metastasis (11/14). Theses results suggest that Pin1 and Wnt signalling pathway are activated in SACC and may play a pivotal role in SACC carcinogenesis and metastasis.
- Subjects :
- Adult
Aged
Carcinoma, Adenoid Cystic secondary
Cell Proliferation
Cyclin D1 genetics
Female
Humans
Male
Middle Aged
NIMA-Interacting Peptidylprolyl Isomerase
RNA, Messenger genetics
Reverse Transcriptase Polymerase Chain Reaction
Salivary Gland Neoplasms pathology
Carcinoma, Adenoid Cystic metabolism
Cyclin D1 metabolism
Peptidylprolyl Isomerase metabolism
Salivary Gland Neoplasms metabolism
beta Catenin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1021-335X
- Volume :
- 16
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Oncology reports
- Publication Type :
- Academic Journal
- Accession number :
- 16865250