Department of Clinical Medicine and Institute of Molecular Medicine, Trinity College Dublin, Dublin 2, Ireland.
Carcinogenesis. 2010 May;31(5):936-45. doi: 10.1093/carcin/bgq036. Epub 2010 Feb 5.
Reflux of gastroduodenal contents and consequent inflammatory responses are associated with the development of Barrett's oesophagus (BO) and the promotion of oesophageal adenocarcinoma (OAC). Deregulation of inflammatory processes is a hallmark of oesophageal cancer. In this study, we aimed to investigate (i) the transcriptional responses to deoxycholic acid (DCA) in cell lines representative of either end of the oesophageal cancer sequence, (ii) the expression of DCA-regulated genes in data charting oesophageal carcinogenesis and (iii) the impact of these genes on oesophageal inflammatory signalling. Gene expression microarrays were utilized to demonstrate differential transcriptional responses between squamous (HET-1A) and adenomatous (SKGT4) cell lines exposed to DCA. Differential basal and DCA-inducible expression of cytokines such as interleukin (IL) 8 was observed between both cell types. A cohort of DCA-regulated genes specific to each cell type was identified in microarray experimentation and subsequently validated. Cell type-specific genes included TRB3, CXCL14, GDF15 and LIF in HET-1A cells, with COX2-, ESM1-, URHF1- and IL1alpha-and IL1beta-specific expression in SKGT4 cells. Over 30% of the genes altered in BO and OAC were shown to be regulated by DCA utilizing an integrative genomic approach. One such gene, tribbles-homology-3 (TRB3) was induced specifically in HET-1A cells, absent in SKGT4 cells and decreased in BO samples in silico and in vivo. Inhibition and re-introduction of TRB3 in HET-1A and SKGT4 cells, respectively, demonstrated the ability of TRB3 to regulate inflammatory signalling through nuclear factor-kappaB. This study identifies mechanisms through which bile acids such as DCA, in conjunction with the loss of key signalling molecules, could regulate oesophageal metaplasticity.
胃十二指肠内容物反流和随之而来的炎症反应与 Barrett 食管 (BO) 的发展和食管腺癌 (OAC) 的促进有关。炎症过程的失调是食管癌的一个标志。在这项研究中,我们旨在研究:(i) 胆汁酸 (DCA) 对代表食管癌序列两端的细胞系的转录反应;(ii) 数据图表中 DCA 调节基因的表达与食管癌变的关系;(iii) 这些基因对食管炎症信号的影响。利用基因表达微阵列来证明暴露于 DCA 的鳞状 (HET-1A) 和腺瘤 (SKGT4) 细胞系之间的转录反应有差异。在这两种细胞类型之间观察到细胞因子如白细胞介素 (IL) 8 的基础和 DCA 诱导的差异表达。在微阵列实验中确定了每个细胞类型特有的 DCA 调节基因的差异表达,并随后进行了验证。细胞类型特异性基因包括 HET-1A 细胞中的 TRB3、CXCL14、GDF15 和 LIF,而 SKGT4 细胞中则特异性表达 COX2、ESM1、URHF1、IL1alpha 和 IL1beta。利用整合基因组学方法,超过 30%的在 BO 和 OAC 中改变的基因被证明受到 DCA 的调节。其中一个基因,TRB3,在 HET-1A 细胞中被特异性诱导,在 SKGT4 细胞中不存在,并且在 BO 样本的体内和体外都被下调。在 HET-1A 和 SKGT4 细胞中分别抑制和重新引入 TRB3,证明了 TRB3 通过核因子-kappaB 调节炎症信号的能力。这项研究确定了胆汁酸(如 DCA)与关键信号分子的丧失相结合,如何调节食管化生的机制。