Edinburgh Breast Unit Research Group, Western General Hospital, Edinburgh, UK.
Pharmacogenomics J. 2012 Feb;12(1):10-21. doi: 10.1038/tpj.2010.67. Epub 2010 Aug 10.
The study aim was to identify early (within 14 days) and late changes (by 3 months) in breast cancer gene expression profiles associated with neoadjuvant therapy with letrozole. RNA from sequential tumour biopsies in 54 patients was analyzed on microarrays; changes were determined by frequency, magnitude and significance analyses. Substantially more genes were changed at 3 months (1503) than at 14 days (237). Early changed genes were associated with cell cycle (downregulation), blood vessel development and extracellular matrix (upregulation); late changes included 'cellular metabolic process', 'generation of precursor metabolites and energy' (decreased) and 'cell adhesion' 'biological adhesion' (increased). A striking difference between the early and late changes was the general location of downregulated genes-nuclear structures at 14 days and mitochondria after 3 months. These changes in gene expression profiles provide a new and important database by which to understand molecular mechanisms of letrozole in breast cancers.
本研究旨在鉴定与来曲唑新辅助治疗相关的乳腺癌基因表达谱的早期(14 天内)和晚期(3 个月时)变化。对 54 例患者的连续肿瘤活检组织的 RNA 进行了微阵列分析;通过频率、幅度和显著性分析确定了变化。3 个月时变化的基因(1503 个)明显多于 14 天时(237 个)。早期变化的基因与细胞周期(下调)、血管生成和细胞外基质(上调)有关;晚期变化包括“细胞代谢过程”、“前体代谢物和能量的产生”(下调)以及“细胞黏附”、“生物黏附”(上调)。早期和晚期变化之间的一个显著差异是下调基因的一般位置——14 天时为核结构,3 个月后为线粒体。这些基因表达谱的变化为理解来曲唑在乳腺癌中的分子机制提供了一个新的重要数据库。