Abstract
DNA-microarray technology has made it possible to simultaneously analyze the expression of thousands of genes in a small sample of tumor tissue. In epithelial ovarian cancer, gene-expression profiling has been used to provide prognostic information, to predict response to first-line platinum-based chemotherapy, and to discriminate between different histologic subtypes. Furthermore, DNA-microarray technology might permit identification of novel markers for early detection of disease and provide insights into the mechanisms of cancer growth and chemotherapy resistance. In this Review, we summarize the contributions of gene-expression profiling to the diagnosis and management of epithelial ovarian cancer and discuss ways in which this technique could become a useful tool in clinical management.
Key Points
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Multigene signatures identified through microarray analysis can predict clinical outcome and response to first-line platinum-based chemotherapy in epithelial ovarian cancer
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DNA-microarray technology has identified several genes that may be implicated in the development of resistance to carboplatin and paclitaxel, but only a few have been validated by functional studies or clinical correlation
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Novel markers potentially useful for early detection of disease can be identified by gene-expression profiling, although such markers have not yet been clinically validated
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Molecular profiles that distinguish between various histologic subtypes of epithelial ovarian cancer, as well as borderline (low malignant potential) tumors, have been discovered by gene-expression profiling
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Acknowledgements
This work was supported in part by LeAnn's Project, by the Bernice Shopkin Weisman Fund, and by the Ovarian Cancer Research Fund in memory of Amy Sachs Simon. This work was also supported by NIH Ovarian Cancer SPORE Grant CA105009.
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Konstantinopoulos, P., Spentzos, D. & Cannistra, S. Gene-expression profiling in epithelial ovarian cancer. Nat Rev Clin Oncol 5, 577–587 (2008). https://doi.org/10.1038/ncponc1178
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DOI: https://doi.org/10.1038/ncponc1178