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利用cDNA微阵列技术发现食管鳞状细胞癌中下调的与Ca2+相关及分化相关基因。

Discovery of Ca2+-relevant and differentiation-associated genes downregulated in esophageal squamous cell carcinoma using cDNA microarray.

作者信息

Luo Aiping, Kong Jianping, Hu Gengxi, Liew Choong-Chin, Xiong Momiao, Wang Xiuqin, Ji Junfang, Wang Tao, Zhi Huiying, Wu Min, Liu Zhihua

机构信息

National Lab of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100021, P.R. China.

出版信息

Oncogene. 2004 Feb 12;23(6):1291-9. doi: 10.1038/sj.onc.1207218.

Abstract

To identify genes that are differentially expressed in human esophageal squamous cell carcinoma (ESCC), we have developed a cDNA microarray representing 34 176 clones to analyse gene expression profiles in ESCC. A total of 77 genes (including 31 novel genes) were downregulated, and 15 genes (including one novel gene) were upregulated in cancer tissues compared with their normal counterparts. Immunohistochemistry and Northern blot analysis were carried out to verify the cDNA microarray results. It was revealed that genes involved in squamous cell differentiation were coordinately downregulated, including annexin I, small proline-rich proteins (SPRRs), calcium-binding S100 proteins (S100A8, S100A9), transglutaminase (TGM3), cytokeratins (KRT4, KRT13), gut-enriched Krupple-like factor (GKLF) and cystatin A. Interestingly, most of the downregulated genes encoded Ca(2+)-binding or -modulating proteins that constitute the cell envelope (CE). Moreover, genes associated with invasion or proliferation were upregulated, including genes such as fibronectin, secreted protein acidic and rich in cystein (SPARC), cathepsin B and KRT17. Functional analysis of the alteration in the expression of GKLF suggested that GKLF might be able to regulate the expression of SPRR1A, SPRR2A and KRT4 in ESCC. This study provides new insights into the role of squamous cell differentiation-associated genes in ESCC initiation and progression.

摘要

为了鉴定在人类食管鳞状细胞癌(ESCC)中差异表达的基因,我们构建了一个包含34176个克隆的cDNA微阵列,以分析ESCC中的基因表达谱。与正常组织相比,癌组织中共有77个基因(包括31个新基因)表达下调,15个基因(包括1个新基因)表达上调。通过免疫组织化学和Northern印迹分析对cDNA微阵列结果进行验证。结果显示,参与鳞状细胞分化的基因协同下调,包括膜联蛋白I、富含脯氨酸的小蛋白(SPRRs)、钙结合S100蛋白(S100A8、S100A9)、转谷氨酰胺酶(TGM3)、细胞角蛋白(KRT4、KRT13)、肠道富集型Krupple样因子(GKLF)和胱抑素A。有趣的是,大多数下调基因编码构成细胞膜(CE)的钙结合或钙调节蛋白。此外,与侵袭或增殖相关的基因上调,包括纤连蛋白、富含半胱氨酸的酸性分泌蛋白(SPARC)、组织蛋白酶B和KRT17等基因。对GKLF表达改变的功能分析表明,GKLF可能能够调节ESCC中SPRR1A、SPRR2A和KRT4的表达。本研究为鳞状细胞分化相关基因在ESCC发生和发展中的作用提供了新的见解。

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