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Genome-wide gene expression profile analysis of esophageal squamous cell carcinomas

机译:食管鳞状细胞癌的全基因组基因表达谱分析

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To identify the molecules involved in esophageal carcinogenesis and those applicable as novel tumor markers and for the development of new molecular therapies, we performed gene expression profile analysis of 19 esophageal squamous cell carcinoma (ESCC) cells purified by laser microbeam microdissection (LMM). Using a cDNA microarray representing 32,256 genes, we identified 147 genes that were commonly up-regulated and 376 transcripts that were down-regulated in ESCC cells compared with non-cancerous esophageal epithelial cells. A comparison of clinicopathological data with the expression profiles of the 19 ESCCs identified 20 genes whose expression levels could most significantly separate cases with lymph node metastasis from those without. In addition, immunohistochemical analysis of candidate tumor markers on tissue microarrays demonstrated transactivation of a secretory protein, transforming growth factor α (TGFA) in the great majority of 228 ESCC cases and an association of their expression with the poor prognosis of patients. Our data provide valuable information for establishing novel diagnostic markers for early diagnosis and choice of therapy, and identifying therapeutic target molecules for the development of novel anti-cancer drugs and immunotherapy in esophageal cancer treatment.
机译:为了鉴定与食道癌发生有关的分子以及可作为新型肿瘤标志物和开发新分子疗法的分子,我们对通过激光微束显微解剖(LMM)纯化的19例食道鳞状细胞癌(ESCC)细胞进行了基因表达谱分析。与代表非癌性食管上皮细胞相比,使用代表32,256个基因的cDNA微阵列,我们在ESCC细胞中鉴定了147个通常被上调的基因和376个被下调的转录物。将临床病理学数据与19个ESCC的表达谱进行比较,确定了20个基因,这些基因的表达水平可以最明显地将有淋巴结转移的病例与没有淋巴结转移的病例区分开。此外,组织芯片上候选肿瘤标记物的免疫组织化学分析表明,在绝大多数228例ESCC病例中,分泌蛋白反式激活,转化生长因子α(TGFA)以及它们的表达与患者预后不良相关。我们的数据为建立用于早期诊断和治疗选择的新型诊断标志物,以及为食管癌治疗中新型抗癌药和免疫疗法的开发确定治疗靶标分子提供了有价值的信息。

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