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TP53 , p14 ARF , p16 INK4a and H-ras gene molecular analysis in intestinal-type adenocarcinoma of the nasal cavity and paranasal sinuses

Authors :
Maria Oggionni
Simona Suardi
Marco A. Pierotti
Federica Perrone
Lisa Licitra
Pasquale Quattrone
Silvana Pilotti
Giulio Cantù
Roberta Romanò
Gabriella Bimbi
Sarah Birindelli
Maria Luisa Moiraghi
Silvia Tabano
Source :
International Journal of Cancer. 105:196-203
Publication Year :
2003
Publisher :
Wiley, 2003.

Abstract

Intestinal-type adenocarcinoma (ITAC) of the nasal cavity and paranasal sinuses is an uncommon tumor associated with occupational exposure to dusts of different origin. Few investigations addressed molecular alterations in ITAC mainly focused on TP53, K-ras and H-ras gene mutations. The occurrence of TP53, p14(ARF) and p16(INK4a) deregulation and H-ras mutations was investigated in 21 consecutive and untreated ITACs cases, 17 with known professional exposure. No H-ras mutations were found. In patients with known exposure, cumulative evidence of TP53 or p14(ARF) alterations accounted for 88% and the evidence of p16(INK4a) alterations for 65%, respectively. TP53 mutations were present in 44% of the ITACs, consisted of G:C-->A:T transitions in 86%, and involved the CpG dinucleotides in 50% of the cases. LOH at the locus 17p13 and an uncommon high rate of p53 stabilization were detected in 58% and 59% of the cases, respectively. p14(ARF)and p16(INK4a) promoter methylation accounted for 80% and 67% respectively, and LOH at the locus 9p21 occurred in 45% of the cases. Interestingly, all dust-exposed tumors with p16(INK4a) alterations shared TP53 or p14(ARF) deregulation. The present results show a close association of this occupational tumor with TP53, p14(ARF) and p16(INK4a) gene deregulation. Given the important role that these genes play in cell growth control and apoptosis, the knowledge of ITAC genetic profile may be helpful in selecting more tailored treatments.

Details

ISSN :
00207136
Volume :
105
Database :
OpenAIRE
Journal :
International Journal of Cancer
Accession number :
edsair.doi...........c3353c9905125d41ad0ddf98c5346232
Full Text :
https://doi.org/10.1002/ijc.11062