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以β-连环蛋白调控为重点的乳腺癌基因表达谱分析。

Gene expression profiling of breast cancers with emphasis of beta-catenin regulation.

作者信息

Roh Mee Sook, Hong Sook Hee, Jeong Jin Sook, Kwon Hyuk Chan, Kim Min Chan, Cho Se Heon, Yoon Jin Han, Hwang Tae Ho

机构信息

Department of Pathology, Dong-A University College of Medicine, Busan, Korea.

出版信息

J Korean Med Sci. 2004 Apr;19(2):275-82. doi: 10.3346/jkms.2004.19.2.275.

Abstract

To gain molecular understanding of carcinogenesis of breast cancer, gene expression profiles were analyzed using cDNA microarray representing 4,600 cDNAs in 10 breast cancer samples and the adjacent noncancerous breast tissues from the same patients. The alterations in gene expression levels were confirmed by reversetranscription PCR in four randomly selected genes. Genes that were differently expressed in cancer and noncancerous tissues were identified. 106 (of which 55 were known) and 49 (of which 28 were known) genes were up- or down-regulated, respectively, in greater than 60% of the breast cancer samples. In cancer tissues, genes related to cell cycle, transcription, metabolism, cell structure/motility and signal transduction were mostly up-regulated. Furthermore, three cancer tissues showing immunohistochemically aberrant accumulation of beta-catenin in the nucleus and/or cytoplasm revealed down-regulation of Siah and Axin genes and up-regulation of Wnt and c-myc genes. These findings were highly consistent with Wnt signaling pathway associated with beta-catenin regulation previously suggested by others. Our studies, therefore, provide not only a molecular basis to understand biological processes of breast cancer but also useful resources to define the mechanism of beta-catenin expression in tumorigenesis of breast cancer.

摘要

为了从分子水平了解乳腺癌的致癌机制,我们使用代表4600个cDNA的cDNA微阵列,对10例乳腺癌样本及其同一患者的癌旁非癌乳腺组织进行了基因表达谱分析。通过逆转录PCR对随机选择的4个基因的基因表达水平变化进行了确认。鉴定出在癌组织和非癌组织中差异表达的基因。在超过60%的乳腺癌样本中,分别有106个(其中55个已知)和49个(其中28个已知)基因上调或下调。在癌组织中,与细胞周期、转录、代谢、细胞结构/运动和信号转导相关的基因大多上调。此外,三个在免疫组织化学上显示β-连环蛋白在细胞核和/或细胞质中异常积累的癌组织,显示Siah和Axin基因下调,Wnt和c-myc基因上调。这些发现与其他人先前提出的与β-连环蛋白调节相关的Wnt信号通路高度一致。因此,我们的研究不仅为理解乳腺癌的生物学过程提供了分子基础,也为确定β-连环蛋白在乳腺癌肿瘤发生中的表达机制提供了有用的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9337/2822311/872ab1d96d32/jkms-19-275-g001.jpg

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