Gene-expression signatures in ovarian cancer: Promise and challenges for patient stratification

被引:29
作者
Konecny, Gottfried E. [1 ]
Winterhoff, Boris [2 ]
Wang, Chen [3 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Hematol Oncol, 100 Med Plaza,Suite 550,Le Conte Ave, Los Angeles, CA 90095 USA
[2] Univ Minnesota, Dept Obstet & Gynecol, Div Gynecol Oncol, Minneapolis, MN 55455 USA
[3] Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
关键词
MOLECULAR SUBTYPES; POOR-PROGNOSIS; CLEAR-CELL; PATTERNS; SURVIVAL; PROFILES; GRADE; CHEMOTHERAPY; VALIDATION; WOMEN;
D O I
10.1016/j.ygyno.2016.01.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microarray-based gene expression studies demonstrate that ovarian cancer is both a clinically diverse and molecularly heterogeneous disease compromising subtypes with distinct gene expression patterns that are each associated with statistically significant different clinical outcomes. The information provided by gene expression based assays is promising and deserves incorporation into clinical decision-making. Further studies are needed to determine which subtype signatures are most appropriate to select patients for a given therapy. This process will require the development of standardized molecular diagnostic assays that can be used for retrospective correlative studies and prospective validations of their clinical utility. Recent advances in assay development for FFPE tissues will facilitate accurate and cost-effective classification of ovarian cancer and help move the evolving molecular classification to clinic. The current review will summarize the development of gene expression based assays in ovarian cancer and will describe how the results of studies to date have expanded our appreciation of the heterogeneity of ovarian cancer. We discuss difficulties in the development and validation of molecular classifications in ovarian cancer and we provide future directions how we may be able to soon classify the disease in a manner that might have greater clinical utility. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:379 / 385
页数:7
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