Pedigree analysis of the oral cancer (OC) patients registered at our C
entre had disclosed familiar aggregation of oral cancer which hitherto
has not been largely reported. There is a paucity of information on t
he genetic determinism for familial oral cancer predisposition. Theref
ore, we investigated constitutional chromosome abnormalities and bleom
ycin-induced chromosome sensitivity of 7 familiar and 10 sporadic oral
cancer patients and 14 unaffected family members (first-degree relati
ves) to determine whether these factors could give any clues regarding
cancer-predisposing factors. Neither the oral cancer patients nor the
unaffected family members showed any constitutional chromosomal abnor
malities. However, with regard to bleomycin sensitivity, there was sig
nificant difference between the oral-cancer patients and unaffected re
latives. The mean b/c value was 1.68 +/- 0.48 for familiar OC patients
, 1.12 +/- 0.36 for sporadic OC patients and 0.52 +/- 0.18 for the una
ffected family members (p < 0.001). A noteworthy observation was that
one unaffected family member also showed bleomycin hypersensitivity an
d expressed a mean b/c value of 1.32, at the initiation of the study.
That patient later developed oral carcinoma. This clearly demonstrates
that mutagen hypersensitivity among unaffected relatives in OC famili
es may be related to cancer predisposition. The mutagen sensitivity st
udy is being continued in a larger series of subjects, for the develop
ment of a cytogenetic marker for prediction of cancer susceptibility.
(C) 1996 Wiley-Liss, Inc.