Hostname: page-component-8448b6f56d-mp689 Total loading time: 0 Render date: 2024-04-23T09:33:54.571Z Has data issue: false hasContentIssue false

Studies of the cell cycle regulatory proteins P16, cyclin D1 and retinoblastoma protein in laryngeal carcinoma tissue

Published online by Cambridge University Press:  08 March 2006

Tomasz Krecicki
Affiliation:
Department of Otolaryngology, Wroclaw Medical University, Poland.
Robert Smigiel
Affiliation:
Department of Pathophysiology, Wroclaw Medical University, Poland.
Marcin Fraczek
Affiliation:
Department of Otolaryngology, Wroclaw Medical University, Poland.
Marlena Kowalczyk
Affiliation:
Department of Basic Medical Sciences, Wroclaw Medical University, Poland.
Maria M. Sasiadek
Affiliation:
Department of Genetics, Wroclaw Medical University, Poland.

Abstract

Defects in the system controlling the cell cycle can lead to an increased proliferation of cancer cells. The aim of this study was to analyse the immunohistochemical expression of chosen cell cycle proteins (P16, cyclin D1 and retinoblastoma protein) and their connection with the clinical course of the disease in laryngeal squamous cell cancer (LSCC). Cancer tissue sections obtained from 58 patients after total laryngectomy served to determine the level of the proteins’ expression using immunohistochemical staining and commercial antibodies. A decreased level of P16 expression in 47 per cent, of retinoblastoma protein in 12 per cent and strong cyclin D1 expression in 48 per cent of cases was revealed. Our results show significant correlation between decreased P16 expression and increased tumour dedifferentiation. Overexpression of cyclin D1 was statistically more common in locally advanced tumours (T3–T4). Low expression of retinoblastoma protein was significantly correlated with both positive P16 immunostaining and with strong cyclin D1 expression. Our study confirms that dysfunction of cell cycle regulation is a common event and may play a significant role in the development of squamous cell carcinoma of the larynx.

Type
Research Article
Copyright
© 2004 Royal Society of Medicine Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)