Chattopadhyay Indranil, Phukan Rupkumar, Singh Avninder, Vasudevan Madavan, Purkayastha Joydeep, Hewitt Stephen, Kataki Amal, Mahanta Jagadish, Kapur Sujala, Saxena Sunita
Institute of Pathology, Safdarjung Hospital Campus, New Delhi-110029, India.
Oncol Rep. 2009 May;21(5):1135-46. doi: 10.3892/or_00000333.
To identify the genes and molecular functional pathways involved in esophageal cancer, we analyzed the gene expression profile of esophageal tumor tissue from patients having family history of esophageal cancer by cDNA microarray. Three hundred and fifty differentially expressed genes (26 up-regulated and 324 down-regulated) were identified. Genes involved in humoral immune response (PF4), extracellular matrix organization (COL4A4), metabolism of xenobiotics (EPHX1), TGF-beta signaling (SMAD1) and calcium signaling pathways (VDAC1) were down-regulated and genes involved in regulation of actin cytoskeleton (WASL), neuroactive ligand receptor interaction (GRM3), Toll-like receptor (CD14), B-cell receptor (IFITM1) and insulin signaling pathways (FOXO1A) were up-regulated. Validation of differential expression of subset of genes by QRT-PCR and tissue microarray in familial and non-familial cases showed no significant difference in expression of these genes in two groups suggesting familial clustering occurs as result of sharing of common environmental factors. Gene expression profiling of clinical specimens from well characterized populations that have familial clustering of cancer identified molecular mechanism associated with progression of esophageal cancer.
为了鉴定与食管癌相关的基因和分子功能通路,我们通过cDNA微阵列分析了有食管癌家族史患者的食管肿瘤组织的基因表达谱。共鉴定出350个差异表达基因(26个上调和324个下调)。参与体液免疫反应(PF4)、细胞外基质组织(COL4A4)、外源性物质代谢(EPHX1)、转化生长因子-β信号通路(SMAD1)和钙信号通路(VDAC1)的基因下调,而参与肌动蛋白细胞骨架调节(WASL)、神经活性配体受体相互作用(GRM3)、Toll样受体(CD14)、B细胞受体(IFITM1)和胰岛素信号通路(FOXO1A)的基因上调。通过定量逆转录聚合酶链反应(QRT-PCR)和组织芯片对家族性和非家族性病例中部分基因差异表达的验证表明,两组中这些基因的表达无显著差异,提示家族聚集是由于共同环境因素的共享所致。对具有癌症家族聚集特征的人群的临床标本进行基因表达谱分析,确定了与食管癌进展相关的分子机制。