Wj. Roy et al., FREQUENT LOSS OF HETEROZYGOSITY ON CHROMOSOME-7 AND CHROMOSOME-9 IN BENIGN EPITHELIAL OVARIAN-TUMORS, Oncogene, 15(17), 1997, pp. 2031-2035
It is presently unclear if ovarian cancers arise through malignant tra
nsformation of pre-existing benign tumours, The apparent rarity of los
s of heterozygosity (LOH) reported for benign tumours has led to specu
lation that they lack malignant potential and represent a biological e
ntity distinct from ovarian carcinoma, We reasoned that the absence of
detectable LOH may be due to the masking of such losses by contaminat
ion with normal tissue present in excess in the majority of benign tum
our biopsies, Therefore we utilized a microdissection technique to exa
mine for LOH using 14 microsatellite markers on chromosome arms 6q, 7p
, 7q, 9p, 11q and 17p in 31 solitary benign epithelial ovarian tumours
, LOH was detected on all chromosome arms with the most frequent LOH o
ccurring on 7p (27%) and 9p (26%), In addition, a point mutation in co
don 157 of TP53 was detected in one tumour which is the first report o
f a TP53 mutation in a solitary benign ovarian tumour, In total 48% of
tumours harboured genetic alterations which supports the idea that al
l benign ovarian tumours may carry a genetic predisposition to maligna
ncy and are therefore not inherently different from their malignant co
unterparts.