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首页> 外文期刊>World Journal of Gastroenterology >Monitoring microarray-based gene expression profile changes in hepatocellular carcinoma.
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Monitoring microarray-based gene expression profile changes in hepatocellular carcinoma.

机译:监测基于微阵列的基因表达谱在肝细胞癌中的变化。

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摘要

AIM: To find out key genes responsible for hepatocarc-inogenesis and to further understand the underlying molecular mechanism through investigating the differential gene expression between human normal liver tissue and hepatocellular carcinoma (HCC). METHODS: DNA microarray was prepared by spotting PCR products of 1 000 human genes including 445 novel genes, 540 known genes as well as 12 positive (housekeeping) and 3 negative controls (plant gene) onto treated glass slides. cDNA probes were prepared by labeling normal liver tissue mRNA and cancer liver tissue mRNA with Cy3-dUTP and Cy5-dUTP separately through reverse transcription. The arrays were hybridized against the cDNA probe and the fluorescent signals were scanned. The data obtained from repeated experiments were analyzed. RESULTS: Among the 20 couple samples investigated (from cancerous liver tissue and normal liver tissue), 38 genes including 21 novel genes and 17 known genes exhibited different expressions. CONCLUSION: cDNA microarray technique is powerful to identify candidate target genes that may play important roles in human carcinogenesis. Further analysis of the obtained genes is helpful to understand the molecular changes in HCC progression and ultimately may lead to the identification of new targets for HCC diagnosis and intervention.
机译:目的:通过研究人类正常肝组织与肝细胞癌(HCC)之间的差异基因表达,找出导致肝癌发生的关键基因,并进一步了解其潜在的分子机制。方法:通过将包含445个新基因,540个已知基因以及12个阳性(管家)和3个阴性对照(植物基因)的1000种人类基因的PCR产物点到经处理的载玻片上来制备DNA微阵列。通过逆转录分别用Cy3-dUTP和Cy5-dUTP标记正常肝组织mRNA和癌肝组织mRNA,制备cDNA探针。将阵列与cDNA探针杂交,并扫描荧光信号。分析了从重复实验获得的数据。结果:在所研究的20对夫妇样本中(癌性肝组织和正常肝组织),38个基因包括21个新基因和17个已知基因表现出不同的表达。结论:cDNA微阵列技术能够强大地鉴定可能在人类致癌作用中发挥重要作用的候选靶基因。对获得的基因的进一步分析有助于了解HCC进展中的分子变化,并最终可能导致鉴定HCC诊断和干预的新靶标。

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