TY - JOUR
T1 - Loss of imprinting and genetic alterations of the cyclin-dependent kinase inhibitor p57(KIP2) gene in head and neck squamous cell carcinoma
AU - Lai, Syeling
AU - Goepfert, Helmuth
AU - Gillenwater, Ann M.
AU - Luna, Mario A.
AU - El-Naggar, Adel K.
PY - 2000/8
Y1 - 2000/8
N2 - The p57(KIP2) is a maternally expressed and paternally imprinted cyclin-dependent kinase inhibitor located on chromosome 11p15.5. Because of its location, biochemical functions, and imprinting status, p57(KIP2) has been considered a candidate tumor suppressor gene. To determine, for the first time, the involvement of this gene in the development of head and neck squamous carcinoma (HNSC), we analyzed the imprinting and expression status and loss of heterozygosity (LOH) within the p57(KIP2) gene flanking loci on the 11p15.5 region in 64 primary untreated tumors. Of the 30 (47%) informative cases for this gene, loss of imprinting and LOH were noted in 4 (13%) and 10 tumors (33%), respectively. Analysis of the microsatellite markers flanking the p57(KIP2) gene on chromosome 11p showed infrequent alterations at these loci. p57(KIP2) was expressed in all tumors with LOH within and around the gene. Quantitative reverse transcription-PCR analysis showed elevated p57 mRNA expression in tumor with loss of imprinting. Sequencing analysis of exons 1 and 2 of the p57(KIP) gene failed to detect any mutations. Our data indicate: (a) infrequent genomic abnormalities at the p57(KIP2) gene in HNSC; (b) leaky or incomplete imprinting of the paternal allele is associated with increased expression of this gene in a subset of tumors; and (c) minimal evidence for suppressor function for this gene in HNSC.
AB - The p57(KIP2) is a maternally expressed and paternally imprinted cyclin-dependent kinase inhibitor located on chromosome 11p15.5. Because of its location, biochemical functions, and imprinting status, p57(KIP2) has been considered a candidate tumor suppressor gene. To determine, for the first time, the involvement of this gene in the development of head and neck squamous carcinoma (HNSC), we analyzed the imprinting and expression status and loss of heterozygosity (LOH) within the p57(KIP2) gene flanking loci on the 11p15.5 region in 64 primary untreated tumors. Of the 30 (47%) informative cases for this gene, loss of imprinting and LOH were noted in 4 (13%) and 10 tumors (33%), respectively. Analysis of the microsatellite markers flanking the p57(KIP2) gene on chromosome 11p showed infrequent alterations at these loci. p57(KIP2) was expressed in all tumors with LOH within and around the gene. Quantitative reverse transcription-PCR analysis showed elevated p57 mRNA expression in tumor with loss of imprinting. Sequencing analysis of exons 1 and 2 of the p57(KIP) gene failed to detect any mutations. Our data indicate: (a) infrequent genomic abnormalities at the p57(KIP2) gene in HNSC; (b) leaky or incomplete imprinting of the paternal allele is associated with increased expression of this gene in a subset of tumors; and (c) minimal evidence for suppressor function for this gene in HNSC.
UR - http://www.scopus.com/inward/record.url?scp=0033902038&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033902038&partnerID=8YFLogxK
M3 - Article
C2 - 10955800
AN - SCOPUS:0033902038
SN - 1078-0432
VL - 6
SP - 3172
EP - 3176
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 8
ER -