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Overexpression of chromatin assembly factor-1 (CAF-1) p60 is predictive of adverse behaviour of prostatic cancer.

Authors :
Staibano, Stefania
Mascolo, Massimo
Mancini, Francesco Paolo
Kisslinger, Annamaria
Salvatore, Gaetano
Di Benedetto, Maria
Chieffi, Paolo
Altieri, Vincenzo
Prezioso, Domenico
Ilardi, Gennaro
De Rosa, Gaetano
Tramontano, Donatella
Source :
Histopathology. Apr2009, Vol. 54 Issue 5, p580-589. 10p. 1 Color Photograph, 2 Black and White Photographs, 1 Chart.
Publication Year :
2009

Abstract

Aims: Prostatic cancer may remain organ-confined indefinitely; in a number of patients, however it gives rise to clinical symptoms and death. The biological behaviour of this tumour mostly remains difficult to predict. A promising tool for diagnosis and prognosis of some human tumours is the chromatin assembly factor-1 (CAF-1), involved in the control of higher order chromatin organization. The aim was to explore the role of CAF-1/p60 protein as a new prognostic marker for prostatic cancer. Methods and results: The expression of CAF-1/p60 was evaluated by immunohistochemistry and Western blotting in a selected series of prostatic cancers and in prostatic cancer cell lines. Results were compared with clinicopathological data and outcome of patients. CAF-1/p60 was expressed in all cases, with a linear increase from low-grade tumours (Gleason score <7) to high-grade prostatic cancers (Gleason score >7). By comparing results with follow-up data, a significant association between overexpression of CAF-1/p60 and unfavourable behaviour of prostatic cancer emerged, and its predictive value was independent of classical prognostic factors. Conclusions: In our series of cases, overexpression of CAF-1/p60 characterized prostatic cancers with a worse prognosis. CAF-1/p60 has a potential role as a new reliable prognostic biomarker for prostatic cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03090167
Volume :
54
Issue :
5
Database :
Academic Search Index
Journal :
Histopathology
Publication Type :
Academic Journal
Accession number :
37370622
Full Text :
https://doi.org/10.1111/j.1365-2559.2009.03266.x