López-Knowles Elena, Gao Qiong, Cheang Maggie Chon U, Morden James, Parker Joel, Martin Lesley-Ann, Pinhel Isabel, McNeill Fiona, Hills Margaret, Detre Simone, Afentakis Maria, Zabaglo Lila, Dodson Andrew, Skene Anthony, Holcombe Chris, Robertson John, Smith Ian, Bliss Judith M, Dowsett Mitch
Royal Marsden Hospital, London, UK.
Breast Cancer Now Research Centre, The Institute of Cancer Research, London, UK.
Breast Cancer Res. 2016 Apr 1;18(1):39. doi: 10.1186/s13058-016-0696-2.
Gene expression is widely used for the characterisation of breast cancers. Variability due to tissue heterogeneity or measurement error or systematic change due to peri-surgical procedures can affect measurements but is poorly documented. We studied the variability of global gene expression between core-cuts of primary ER+ breast cancers and the impact of delays to tissue stabilisation due to sample X-ray and of diagnostic core cutting.
Twenty-six paired core-cuts were taken immediately after tumour excision and up to 90 minutes delay due to sample X-ray; 57 paired core-cuts were taken at diagnosis and 2 weeks later at surgical excision. Whole genome expression analysis was conducted on extracted RNA. Correlations and differences were assessed between the expression of individual genes, gene sets/signatures and intrinsic subtypes.
Twenty-three and 56 sample pairs, respectively, were suitable for analysis. The range of correlations for both sample sets were similar with the majority being >0.97 in both. Correlations between pairs for 18 commonly studied genes were also similar between the studies and mainly with Pearson correlation coefficients >0.6 except for a small number of genes, which had a narrow-dynamic range (e.g. MKI67, SNAI2). There was no systematic difference in intrinsic subtyping between the first and second sample of either set but there was c.15 % discordance between the subtype assignments between the pairs, mainly where the subtyping of individual samples was less certain. Increases in the expression of several stress/early-response genes (e.g. FOS, FOSB, JUN) were found in both studies and confirmed findings in earlier smaller studies. Increased expression of IL6, IGFBP2 and MYC (by 17 %, 14 % and 44 %, respectively) occurred between the samples taken 2 weeks apart and again confirmed findings from an earlier study.
There is generally good correlation in gene expression between pairs of core-cuts except where genes have a narrow dynamic range. Similar correlation coefficients to the average gene expression profiles of intrinsic subtype, particularly LumA and LumB, can lead to discordances between assigned subtypes. Substantial changes in expression of early-response genes occur within an hour after surgery and in IL6, IGFB2 and MYC as a result of diagnostic core-cut biopsy.
Trial number CRUK/07/015 . Study start date September 2008.
基因表达广泛应用于乳腺癌的特征描述。由于组织异质性、测量误差或围手术期操作导致的系统变化所引起的变异性会影响测量结果,但相关记录较少。我们研究了原发性雌激素受体阳性(ER+)乳腺癌的核心穿刺样本之间整体基因表达的变异性,以及样本X射线检查导致的组织稳定延迟和诊断性核心穿刺的影响。
在肿瘤切除后立即采集26对核心穿刺样本,由于样本X射线检查最多延迟90分钟;在诊断时采集57对核心穿刺样本,并在手术切除2周后再次采集。对提取的RNA进行全基因组表达分析。评估个体基因、基因集/特征和内在亚型表达之间的相关性和差异。
分别有23对和56对样本适合进行分析。两个样本集的相关性范围相似,大多数相关性均>0.97。两项研究中18个常用研究基因的样本对之间的相关性也相似,除少数具有窄动态范围的基因(如MKI67、SNAI2)外,主要Pearson相关系数>0.6。两组的第一个和第二个样本之间在内在亚型分类上没有系统差异,但样本对之间的亚型分配存在约15%的不一致,主要是在个体样本的亚型分类不太确定的情况下。在两项研究中均发现几种应激/早期反应基因(如FOS、FOSB、JUN)的表达增加,并证实了早期较小规模研究的结果。相隔2周采集的样本之间,IL6、IGFBP2和MYC的表达分别增加了17%、14%和44%,再次证实了早期研究的结果。
除了那些具有窄动态范围的基因外,核心穿刺样本对之间的基因表达通常具有良好的相关性。与内在亚型(特别是LumA和LumB)的平均基因表达谱相似的相关系数可能导致指定亚型之间的不一致。手术后一小时内以及由于诊断性核心穿刺活检,早期反应基因的表达会发生显著变化,IL6、IGFB2和MYC的表达也会发生变化。
试验编号CRUK/07/015。研究开始日期为2008年9月。