C. Huiping et al., HIGH-FREQUENCY OF LOH AT CHROMOSOME 18Q IN HUMAN BREAST-CANCER - ASSOCIATION WITH HIGH S-PHASE FRACTION AND LOW PROGESTERONE-RECEPTOR CONTENT, Anticancer research, 18(2A), 1998, pp. 1031-1036
Human primary breast cancers were analysed for somatic loss of heteroz
ygosity (LOH) at chromosome 18 with 15 polymorphic microsatellite mark
ers. LOH was observed in 148 of the 228 cases analyzed (65%). Three sm
allest common deletion regions (SCDR) were detected on the long arm of
chromosome 18. The marker D18S51 at the region 18q22 showed the highe
st LOH (42%). Tumors with and without LOH at 18q were tested for assoc
iation with clinico-pathological features of the tumors, such as estro
gen and progesterone receptor content, age at diagnosis, tumor size, n
ode status, histological type, S-phase fraction DNA ploidy and LOH at
other chromosomal regions. A significant association was found between
LOH at 18q and high S-phase fraction (99.9% confidence interval) and
low progesterone receptor. content (99%, confidence interval). Further
more, an association was found between LOH at 18q and LOH at 1p, 7q, 9
p, 13q and 17q. We conclude that there are three separate LOH target r
egions at chromosome 18q and that inactivation of one or. mole genes a
t these regions might be important for human breast carcinogenesis.