Suppr超能文献

人肝内胆管癌基因表达的全基因组分析。

Genome-wide analysis of gene expression in human intrahepatic cholangiocarcinoma.

作者信息

Obama Kazutaka, Ura Katsuaki, Li Meihua, Katagiri Toyomasa, Tsunoda Tatsuhiko, Nomura Akinari, Satoh Seiji, Nakamura Yusuke, Furukawa Yoichi

机构信息

Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

出版信息

Hepatology. 2005 Jun;41(6):1339-48. doi: 10.1002/hep.20718.

Abstract

Intrahepatic cholangiocarcinoma is a neoplasm arising in the liver, and its incidence is increasing in Japan as well as in Western countries. Prognosis of patients with this type of tumor remains unsatisfactory because no effective chemotherapeutic drugs are available, we have no sensitive tumor markers to detect this tumor in its early stage, and it is difficult to identify a high-risk group for the disease. To clarify the molecular mechanism of tumorigenesis and identify molecular targets for diagnosis and treatment, we analyzed global gene-expression profiles of 25 intrahepatic cholangiocarcinomas using tumor cell populations purified by laser microbeam microdissection and a cDNA microarray containing 27,648 genes. We identified 52 genes that were commonly upregulated and 421 that were downregulated in intrahepatic cholangiocarcinomas compared with noncancerous biliary epithelial cells. From the 52 upregulated genes, we selected P-cadherin and survivin for further investigation and corroborated enhanced expression of their products in cancer tissues by immunohistochemical staining. Furthermore, comparison between tumors with lymph node metastasis and those without metastasis identified 30 genes that were associated with lymph node involvement. In conclusion, these data should be helpful for a better understanding of the tumorigenesis of intrahepatic cholangiocarcinoma and should contribute to the development of diagnostic and therapeutic strategies for this type of tumor. Supplementary material for this article can be found on the HEPATOLOGY website (http://www.interscience.wiley.com/jpages/0270-9139/suppmat/index.html).

摘要

肝内胆管癌是一种起源于肝脏的肿瘤,在日本以及西方国家其发病率都在上升。由于缺乏有效的化疗药物,没有敏感的肿瘤标志物用于早期检测这种肿瘤,并且难以识别该疾病的高危人群,这类肿瘤患者的预后仍然不尽人意。为了阐明肿瘤发生的分子机制并确定诊断和治疗的分子靶点,我们使用激光微束显微切割纯化的肿瘤细胞群体和包含27,648个基因的cDNA微阵列,分析了25例肝内胆管癌的全基因组表达谱。与非癌性胆管上皮细胞相比,我们鉴定出52个在肝内胆管癌中共同上调的基因和421个下调的基因。从这52个上调基因中,我们选择了P-钙黏蛋白和生存素进行进一步研究,并通过免疫组织化学染色证实了它们的产物在癌组织中的表达增强。此外,有淋巴结转移的肿瘤与无转移的肿瘤之间的比较确定了30个与淋巴结受累相关的基因。总之,这些数据应有助于更好地理解肝内胆管癌的肿瘤发生,并应为这类肿瘤的诊断和治疗策略的发展做出贡献。本文的补充材料可在《肝脏病学》网站(http://www.interscience.wiley.com/jpages/0270-9139/suppmat/index.html)上找到。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验