Variation in gene expression patterns in effusions and primary tumors from serous ovarian cancer patients

被引:21
|
作者
Schaner, Marci E.
Davidson, Ben
Skrede, Martina
Reich, Reuven
Florenes, Vivi Ann
Risberg, Bjorn
Berner, Aasmund
Goldberg, Iris
Givant-Horwitz, Vered
Trope, Claes G.
Kristensen, Gunnar B.
Nesland, Jahn M.
Borresen-Dale, Anne-Lise [1 ]
机构
[1] Univ Oslo, Norwegian Radium Hosp, Dept Genet, N-0310 Oslo, Norway
[2] Stanford Univ, Sch Med, Dept Biochem MES, Stanford, CA 94305 USA
[3] Univ Oslo, Norwegian Radium Hosp, Dept Pathol, N-0310 Oslo, Norway
[4] Hebrew Univ Jerusalem, Fac Med, Dept Pharmacol & Expt Therapeut, IL-91120 Jerusalem, Israel
[5] Univ Oslo, Norwegian Radium Hosp, Dept Gynecol Oncol, N-0310 Oslo, Norway
关键词
D O I
10.1186/1476-4598-4-26
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: While numerous studies have characterized primary ovarian tumors, little information is available regarding expression patterns of metastatic sites of this cancer. To define sets of genes that distinguish primary and metastatic ovarian tumors, we used cDNA microarrays to characterize global gene expression patterns in 38 effusions ( 28 peritoneal, 10 pleural) and 8 corresponding primary ovarian tumors, and searched for associations between expression patterns and clinical parameters. Results: We observed multidimensional variation in expression patterns among the cancers. Coordinate variation in expression of genes from two chromosomal regions, 8q and 19q, was seen in subsets of the cancers indicating possible amplifications in these regions. A set of 112 unique genes of known function was differentially expressed between primary tumors and effusions using supervised analysis. Relatively few differences were seen between effusions isolated from the pleural and peritoneal cavities or between effusions from patients diagnosed with stage III and stage IV cancers. A set of 84 unique genes was identified that distinguished high from lower grade ovarian cancers. The results were corroborated using immunocytochemistry, mRNA in situ hybridization, and immunoblotting. Conclusion: The extensive variation in expression patterns observed underscores the molecular heterogeneity of ovarian cancer, but suggests a similar molecular profile for ovarian carcinoma cells in serosal cavities.
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页数:14
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