六氯环己烷
癌变
生物
基因
肝细胞癌
微阵列
DNA微阵列
表型
互补DNA
基因组
癌症研究
基因表达
微阵列分析技术
遗传学
作者
Hiroshi Okabe,Seiji Satoh,Tatsushi Kato,Osamu Kitahara,Renpei Yanagawa,Yoshio Yamaoka,Tatsuhiko Tsunoda,Yoichi Furukawa,Yusuke Nakamura
出处
期刊:PubMed
日期:2001-03-01
卷期号:61 (5): 2129-37
被引量:545
摘要
To disclose detailed genetic mechanisms in hepatocellular carcinoma (HCC) with a view toward development of novel therapeutic targets, we analyzed expression profiles of 20 primary HCCs and their corresponding noncancerous tissues by means of cDNA microarrays consisting of 23,040 genes. Up-regulation of mitosis-promoting genes was observed in the majority of the tumors examined. Some genes showed expression patterns in hepatitis B virus-positive HCCs that were different from those in hepatitis C virus-positive HCCs; most of them encoded enzymes that metabolize carcinogens and/or anticancer agents. Furthermore, we identified a number of genes associated with malignant histological type or invasive phenotype. Accumulation of such data will make it possible to define the nature of individual tumors, to provide clues for identifying new therapeutic targets, and ultimately to optimize treatment of each patient.
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