PRESENCE OF MULTIPLE INCONTIGUOUS DELETED REGIONS AT THE LONG ARM OF CHROMOSOME-18 IN HEAD AND NECK-CANCER

Citation
Va. Papadimitrakopoulou et al., PRESENCE OF MULTIPLE INCONTIGUOUS DELETED REGIONS AT THE LONG ARM OF CHROMOSOME-18 IN HEAD AND NECK-CANCER, Clinical cancer research, 4(3), 1998, pp. 539-544
Citations number
37
Categorie Soggetti
Oncology
Journal title
ISSN journal
10780432
Volume
4
Issue
3
Year of publication
1998
Pages
539 - 544
Database
ISI
SICI code
1078-0432(1998)4:3<539:POMIDR>2.0.ZU;2-3
Abstract
The 18q chromosomal region is frequently lost in head and neck squamou s cell carcinomas (HNSCCs), Several candidate tumor suppressor genes h ave been mapped to this chromosomal region, including DCC, DPC4, and M ADR2, The latter two genes are members of the Smad family, key downstr eam mediators in the transforming growth factor beta signaling pathway , and their alterations could confer resistance to transforming growth factor beta and contribute to tumorigenesis. Nevertheless, genetic al terations of DCC and DPC4 in HNSCC have not been frequently reported, To further investigate the extent and significance of the loss of the 18q chromosomal region in HNSCC, we performed detailed mapping at this region in a set of 50 primary HNSCCs using 19 highly polymorphic micr osatellite markers, We detected loss of heterozygosity in 84% of the t umors tested and were able to identify three minimal deleted regions e ncompassing markers D18S467-D18S474 at 18q12 (4 cM), D18S1099-D18S487 at 18q21.1 (3 cM), and D18S69-41 at 18q21.1-q21.2 (2 cM), Of these min imal deleted regions, only one harbors a known candidate tumor suppres sor gene, DCC, which maps telomeric to D18S46. In addition, the role o f the MADR2 gene in HNSCCs was investigated by examining nine HNSCC ce ll lines for alterations of the gene by reverse transcription-PCR and direct sequencing analysis, No mutations or polymorphisms were detecte d, making this gene an unlikely target of the frequent loss at 18q in HNSCC, Our data indicate high frequency of loss of heterozygosity at 1 8q in HNSCC and the presence of at least two as yet unidentified tumor suppressor genes in this chromosomal region, Additional efforts to id entify these putative tumor suppressor genes are warranted.