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p21WAF1/Cip1 expression is associated with cell differentiation but not with p53 mutations in squamous cell carcinomas of the larynx.

Authors :
Nadal A
Jares P
Cazorla M
Fernández PL
Sanjuan X
Hernandez L
Pinyol M
Aldea M
Mallofré C
Muntané J
Traserra J
Campo E
Cardesa A
Source :
The Journal of pathology [J Pathol] 1997 Oct; Vol. 183 (2), pp. 156-63.
Publication Year :
1997

Abstract

p21WAF1/Cip1 is a recently identified gene involved in cell cycle regulation through cyclin-CDK-complex inhibition. The expression of this gene in several cell lines seems to be induced by wild-type, but not mutant, p53. p21WAF1/Cip1 expression has been studied at both mRNA and protein levels in a series of 49 normal mucosae and squamous cell carcinomas of the larynx. A significant association was found between mRNA and protein expression in tumours (P < 0.0001). p21WAF1/Cip1 expression was strongly associated with squamous cell differentiation of carcinomas, because six of seven (86 per cent) undifferentiated carcinomas (grade 4) showed very low levels of p21WAF1/Cip1 expression, whereas 41 out of 42 (98 per cent) carcinomas with squamous cell differentiation (grades 1-3) had normal or high levels of p21WAF1/Cip1 expression (P < 0.0001). In addition, p21WAF1/Cip1 expression was topologically related to the squamous differentiation of tumour cells with a distribution similar to that seen in normal squamous epithelium. No correlation was found between p21WAF1/Cip1 expression and the global S-phase of the carcinomas. p53 mutations (exons 5-9) were found in ten carcinomas with p21WAF1/Cip1 expression, but no p53 mutations were detected in three p21WAF1/Cip1-negative tumours. In conclusion, p21WAF1/Cip1 expression is frequently upregulated in squamous cell carcinomas of the larynx and is associated with tumour cell differentiation. p21WAF1/Cip1 expression in these tumours is independent of p53 gene mutations.

Details

Language :
English
ISSN :
0022-3417
Volume :
183
Issue :
2
Database :
MEDLINE
Journal :
The Journal of pathology
Publication Type :
Academic Journal
Accession number :
9390027
Full Text :
https://doi.org/10.1002/(SICI)1096-9896(199710)183:2<156::AID-PATH908>3.0.CO;2-O