Recent investigations revealed that the 9p arm and 17q arm of human ch
romosomes harbour tumour suppressor genes (TSGs) with an important rol
e in multistage carcinogenesis. At the 9p arm is located the p16 (MTS1
) TSG and probably others with an effect on various human tumours such
as acute lymphoblastic leukaemia, bladder cancer, gliomas, malignant
mesotheliomas, melanomas and non-small cell lung carcinomas. In additi
on, the 17q arm harbours BRCA1 TSG which is responsible for approximat
ely 80% of the familial breast/ovarian cancer cases. In order to inves
tigate the implication of these novel TSGs in the development of laryn
geal cancer we performed a loss of heterozygosity (LOH) analysis with
10 polymorphic microsatellite markers (three at the 17q arm surroundin
g the BRCA1 region and seven at the 9p arm). Fourteen of the 17 (82%)
tumours exhibited deletions at 9p, The highest incidence of LOH (6/13,
46%) was found for the marker D9S157 at 9p22. One sample exhibited de
letion of all the informative markers tested indicating deletion of th
e complete 9p arm. No homozygous deletions were found, LOH at the 17q
arm near the BRCA1 locus was found in 6 (35%) among 17 specimens. The
results of this study indicate that allelic deletions at 9p are freque
nt in the development of laryngeal rumours. The highest incidence of L
OH was found for the marker D9S157 which is near, but distinct from th
e location of p16 (MTS1) tumour suppressor gene, indicating the presen
ce of multiple tumour suppressor genes within this chromosomal region.
In addition, BRCA1 TSG is implicated in the development of laryngeal
rumours.