Enhanced expression of vimentin in motile prostate cell lines and in poorly differentiated and metastatic prostate carcinoma.
Authors
Lang, Shona HHyde, Catherine
Reid, Ian N
Hitchcock, Ian S
Hart, Claire A
Bryden, A A G
Villette, Jean-Marie
Stower, Michael J
Maitland, Norman J
Affiliation
YCR Cancer Research Unit, University of York, Heslington, York, United Kingdom. SHL@york.ac.ukIssue Date
2002-09-01
Metadata
Show full item recordAbstract
BACKGROUND: The metastatic potential of a series of prostate cell lines was analysed by measuring motility and invasiveness, and further correlated to the expression of epithelial differentiation markers. METHODS: Invasion and motility were measured using in vitro assays. Immunohistochemistry of cell lines and tissues was used to identify expression of cytokeratins 8 and 1, 5, 10, 14, vimentin, prostate specific antigen, prostate specific membrane antigen, androgen receptor, desmoglein, E-cadherin, beta1 integrin, CD44, hmet, vinculin and actin. RESULTS: Expression of vimentin was the only marker to correlate with motility, no markers correlated to invasion. Lower vimentin expression was observed in cells with low motility (PNT2-C2) and high expression in cells with high motility (P4E6, PNT1a, PC-3). Vimentin expression was not detected in well differentiated tumours, moderately differentiated tumours contained vimentin positive cells (1/9 bone scan negative, 2/5 bone scan positive), but the majority of poorly differentiated cancers (4/11 bone scan negative, 9/14 bone scan positive) and bone metastases (7/8) had high vimentin expression in tumour cells. CONCLUSIONS: Motile prostate cancer cell lines express vimentin. In tissue sections, the presence of vimentin positive tumour cells correlated positively to poorly differentiated cancers and the presence of bone metastases.Citation
Enhanced expression of vimentin in motile prostate cell lines and in poorly differentiated and metastatic prostate carcinoma. 2002, 52 (4):253-63 ProstateJournal
The ProstateDOI
10.1002/pros.10088PubMed ID
12210485Type
ArticleLanguage
enISSN
0270-4137ae974a485f413a2113503eed53cd6c53
10.1002/pros.10088
Scopus Count
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