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Differentiating pancreatic lesions by microarray and QPCR analysis of pancreatic juice RNAs.

机译:通过微阵列和胰腺液RNA的QPCR分析区分胰腺病变。

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BACKGROUND: The gene expression profile of pancreatic cancer is significantly different from that of normal pancreas. Differences in gene expression are detectable using microarrays, but microarrays have traditionally been applied to pancreatic cancer tissue obtained from surgical resection. We hypothesized that gene expression alterations indicative of pancreatic cancer can be detected by profiling the RNA of pancreatic juice. METHODS: We performed oligonucleotide microarray analysis on RNA isolated from pancreatic juice obtained endoscopically after secretin stimulation from six patients with pancreatic cancer and ten patients with nonneoplastic diseases of the pancreas or upper gastrointestinal tract. Extracted RNA was subjected to two rounds of linear RNA amplification, and then hybridized with U133A or X3P gene chips (Affymetrix). RESULTS: Using the U133A or X3P chips, 37 and 133 gene fragments respectively, were identified as being at least 3-fold more abundant in the pancreatic juice of patientswith pancreatic cancer compared to the noncancer controls (p<0.05, Mann-Whitney test). For example, pancreatic juice from patients with pancreatic cancer contained increased levels of IL8, IFITM1, fibrinogen, osteopontin, CXCR4, DAF and NNMT RNA, genes that have been previously reported as overexpressed in primary pancreatic cancers or pancreatic cancer cell lines relative to control tissues. CONCLUSIONS: These results demonstrate that RNA analysis of pancreatic juice can reveal some of the same RNA alterations found in invasive pancreatic cancers. RNA analysis of pancreatic juice deserves further investigation to determine its utility as a tool for the evaluation of pancreatic lesions.
机译:背景:胰腺癌的基因表达谱与正常胰腺的显着不同。使用微阵列可以检测到基因表达的差异,但是传统上微阵列已应用于从手术切除中获得的胰腺癌组织。我们假设可以通过分析胰腺汁的RNA来检测到指示胰腺癌的基因表达改变。方法:我们对6例胰腺癌和10例胰腺或上消化道非肿瘤性疾病的促胰液素刺激后经内窥镜检查的胰液中的RNA进行了寡核苷酸微阵列分析。将提取的RNA进行两轮线性RNA扩增,然后与U133A或X3P基因芯片(Affymetrix)杂交。结果:使用U133A或X3P芯片,与非癌对照相比,胰腺癌患者的胰液中分别含有37和133个基因片段,其丰富度至少高3倍(p <0.05,Mann-Whitney测试) 。例如,来自胰腺癌患者的胰液中IL8,IFITM1,纤维蛋白原,骨桥蛋白,CXCR4,DAF和NNMT RNA的含量增加,这些基因先前已报道在原发性胰腺癌或胰腺癌细胞系中相对于对照组织过表达。结论:这些结果表明胰腺液的RNA分析可以揭示在浸润性胰腺癌中发现的某些相同的RNA改变。胰腺液的RNA分析值得进一步研究,以确定其作为评估胰腺病变的工具的效用。

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