Iddawela Mahesh, Rueda Oscar, Eremin Jenny, Eremin Oleg, Cowley Jed, Earl Helena M, Caldas Carlos
Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge, CB2 0RE, UK.
Department of Oncology, University of Cambridge, Addenbrooke's Hospital, Hills Road, Cambridge, UK.
BMC Genomics. 2017 Jul 11;18(1):526. doi: 10.1186/s12864-017-3867-3.
An absence of reliable molecular markers has hampered individualised breast cancer treatments, and a major limitation for translational research is the lack of fresh tissue. There are, however, abundant banks of formalin-fixed paraffin-embedded (FFPE) tissue. This study evaluated two platforms available for the analysis of DNA copy number and gene expression using FFPE samples.
The cDNA-mediated annealing, selection, extension, and ligation assay (DASL™) has been developed for gene expression analysis and the Molecular Inversion Probes assay (Oncoscan™), were used for copy number analysis using FFPE tissues. Gene expression and copy number were evaluated in core-biopsy samples from patients with breast cancer undergoing neoadjuvant chemotherapy (NAC).
Forty-three core-biopsies were evaluated and characteristic copy number changes in breast cancers, gains in 1q, 8q, 11q, 17q and 20q and losses in 6q, 8p, 13q and 16q, were confirmed. Regions that frequently exhibited gains in tumours showing a pathological complete response (pCR) to NAC were 1q (55%), 8q (40%) and 17q (40%), whereas 11q11 (37%) gain was the most frequent change in non-pCR tumours. Gains associated with poor survival were 11q13 (62%), 8q24 (54%) and 20q (47%). Gene expression assessed by DASL correlated with immunohistochemistry (IHC) analysis for oestrogen receptor (ER) [area under the curve (AUC) = 0.95], progesterone receptor (PR)(AUC = 0.90) and human epidermal growth factor type-2 receptor (HER-2) (AUC = 0.96). Differential expression analysis between ER+ and ER- cancers identified over-expression of TTF1, LAF-4 and C-MYB (p ≤ 0.05), and between pCR vs non-pCRs, over-expression of CXCL9, AREG, B-MYB and under-expression of ABCG2.
This study was an integrative analysis of copy number and gene expression using FFPE core biopsies and showed that molecular marker data from FFPE tissues were consistent with those in previous studies using fresh-frozen samples. FFPE tissue can provide reliable information and will be a useful tool in molecular marker studies.
Trial registration number ISRCTN09184069 and registered retrospectively on 02/06/2010.
缺乏可靠的分子标志物阻碍了乳腺癌的个体化治疗,而转化研究的一个主要限制是缺乏新鲜组织。然而,有大量福尔马林固定石蜡包埋(FFPE)组织库。本研究评估了两种可用于使用FFPE样本分析DNA拷贝数和基因表达的平台。
已开发出用于基因表达分析的cDNA介导的退火、选择、延伸和连接分析(DASL™),并使用分子倒置探针分析(Oncoscan™)对FFPE组织进行拷贝数分析。对接受新辅助化疗(NAC)的乳腺癌患者的芯针活检样本进行基因表达和拷贝数评估。
评估了43例芯针活检样本,确认了乳腺癌中特征性的拷贝数变化,即1q、8q、11q、17q和20q的增益以及6q、8p、13q和16q的缺失。对NAC显示病理完全缓解(pCR)的肿瘤中频繁出现增益的区域为1q(55%)、8q(40%)和17q(40%),而11q11(37%)的增益是未达到pCR的肿瘤中最常见的变化。与生存不良相关的增益为11q13(62%)、8q24(54%)和20q(47%)。通过DASL评估的基因表达与雌激素受体(ER)的免疫组织化学(IHC)分析相关[曲线下面积(AUC)=0.95]、孕激素受体(PR)(AUC=0.90)和人表皮生长因子2型受体(HER-2)(AUC=0.96)。ER+和ER-癌症之间的差异表达分析确定了TTF1、LAF-4和C-MYB的过表达(p≤0.05),以及pCR与未达到pCR的癌症之间CXCL9、AREG、B-MYB的过表达和ABCG2的低表达。
本研究是对FFPE芯针活检样本的拷贝数和基因表达进行的综合分析,结果表明FFPE组织的分子标志物数据与先前使用新鲜冷冻样本的研究结果一致。FFPE组织可提供可靠信息,将成为分子标志物研究中的有用工具。
试验注册号ISRCTN09184069,于2010年6月2日进行回顾性注册。