Genome-wide Gene Expression Profiling of Formalin-fixed Paraffin-Embedded Breast Cancer Core Biopsies Using Microarrays

被引:24
作者
Budczies, Jan [1 ]
Weichert, Wilko [1 ]
Noske, Aurelia [1 ]
Mueller, Berit Maria [1 ]
Weller, Claudia [2 ]
Wittenberger, Timo [2 ]
Hofmann, Hans-Peter [2 ]
Dietel, Manfred [1 ]
Denkert, Carsten [1 ]
Gekeler, Volker [2 ]
机构
[1] Charite, Inst Pathol, D-10117 Berlin, Germany
[2] Nycomed GmbH, Constance, Germany
关键词
breast cancer; formalin-fixed paraffin-embedded samples; core needle biopsies; gene expression; DNA microarray; ESTROGEN-RECEPTOR STATUS; TOPOISOMERASE-II-ALPHA; RNA; DOCETAXEL; SAMPLES; CYCLOPHOSPHAMIDE; AMPLIFICATION; CHEMOTHERAPY; DOXORUBICIN; STATISTICS;
D O I
10.1369/jhc.2010.956607
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The routine workflow for invasive cancer diagnostics includes biopsy processing by formalin fixation and paraffin embedding. It has been shown only recently that this kind of sample can be used for gene expression analysis with microarrays. To support this view, the authors conducted a microarray study using formalin-fixed paraffin-embedded (FFPE) core needle biopsies from breast cancers. Typically, for the 3'-biased chip type that was used, the probe sets interrogate sequences near the poly-A-tail of the transcripts, and this kind of probe turned out to be suitable to measure RNA levels in FFPE biopsies. For ER and HER2, the authors observed strong correlations between RNA levels and protein expression (p = 0.000003 and p = 0.0022). ER and HER2 classification of the biopsies by the RNA levels was feasible with high sensitivity and specificity (AUROC = 0.93 and AUROC = 0.96). Furthermore, a signature of 346 genes was identified that correlated with ER and a signature of 528 genes that correlated with HER2 protein status. Many of these genes (ER: 63%) could be confirmed by analysis of gene expression data from frozen tissues. The findings support the notion that clinically relevant information can be gained from microarray analyses of FFPE cancer biopsies. This opens new opportunities for biomarker detection studies and the integration of microarrays into the workflow of cancer diagnostics. (J Histochem Cytochem 59:146-157, 2011)
引用
收藏
页码:146 / 157
页数:12
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