The majority of ovarian tumors arise from the transformation of the ovarian
surface epithelial cells, a single layer of cells surrounding the ovary, T
o identify genes that may contribute to the malignant phenotype of ovarian
cancers, cDNA representational difference analysis was used to compare expr
essed genes in primary cultures of normal human ovarian surface epithelium
(HOSE) and ovarian tumor-derived epithelial cells from the Cedars-Sinai Ova
rian Cancer (CSOC) repository, A total of 255 differentially expressed gene
s were identified, of which 160 and 95 were specifically expressed in HOSE
and CSOC cells, respectively, Using cDNA array hybridization, the expressio
n profiles of the genes identified by cDNA-representational difference anal
ysis were examined in an additional 5 HOSE and 10 CSOC lines. The compariso
n of average signal of each gene revealed 44 HOSE-specific and 16 CSOC-spec
ific genes that exhibited at least a 2.5-fold difference in expression, A l
arge number of genes identified in this study encode membrane-associated or
secreted proteins and, hence, may be useful as targets in the development
of serum-based diagnostic markers for ovarian cancer. Very few genes associ
ated with protein synthesis or metabolism were identified in this study, re
flecting the lack of observable differences in phenotypic or growth charact
eristics between HOSE and CSOC cells, Northern blot analysis on a subset of
these genes demonstrated comparable levels of gene expression as observed
in the cDNA array hybridization.