Department of General Surgery, China-Japan Friendship Hospital, Beijing, P.R. China.
Surgery. 2011 Jun;149(6):783-91. doi: 10.1016/j.surg.2010.12.007. Epub 2011 Feb 18.
Our aim was to identify differential expression of genes in hepatocellular carcinoma (HCC) with the ultimate goal of discovering novel diagnostic and therapeutic targets.
We examined differences in gene expression between HCC and noncancerous liver tissue using a cDNA array with probes for 15,843 genes/clones. Two genes, osteopontin (OPN) and S100A6, were found to be >10-fold differentially expressed, and were selected for further immunohistochemical staining in 51 HCC and 10 nonmalignant liver specimens. The relation between OPN and S100A6 alterations and various clinicopathologic parameters was also evaluated.
We found a total of 219 genes that were differentially expressed >3-fold. Of these, 109 were upregulated and 110 downregulated. Within this group, 123 genes, including 59 upregulated and 64 downregulated, had been identified previously. These known genes were mainly involved in cell migration, cytoskeleton dynamics, the signaling pathway and cell cycle, and metabolism. OPN expression and S100A6 expression were seen in 26 of 51 (51.0 %) and 16 of 51 (31.4 %) HCC samples, respectively. More importantly, proteins coded by these genes were not found in any noncancerous liver specimen by immunohistochemical analysis. Expression of these genes correlated with poor differentiation (OPN: P = .013; S100A6: P = .008).
OPN, a secreted phosphoprotein that has been increasingly implicated in the progression and metastasis of cancer, and S100A6, a member of the S100 protein family that can perform cell proliferation, differentiation, migration, and cytoskeletal dynamics, may be promising diagnostic markers and therapeutic targets for HCC. In addition, the results encourage future studies involving the roles of these proteins in the development and progression of this cancer.
我们的目的是鉴定肝癌(HCC)中基因的差异表达,最终目标是发现新的诊断和治疗靶点。
我们使用 cDNA 芯片检查 HCC 与非癌性肝组织之间的基因表达差异,该芯片的探针用于 15843 个基因/克隆。发现骨桥蛋白(OPN)和 S100A6 两个基因的表达差异> 10 倍,选择这两个基因进一步对 51 例 HCC 和 10 例非恶性肝标本进行免疫组织化学染色。还评估了 OPN 和 S100A6 改变与各种临床病理参数之间的关系。
我们共发现 219 个差异表达> 3 倍的基因。其中,上调基因 109 个,下调基因 110 个。在这一组中,包括 59 个上调和 64 个下调的基因,以前已经确定了 123 个基因。这些已知基因主要参与细胞迁移、细胞骨架动力学、信号通路和细胞周期以及代谢。在 51 例 HCC 样本中,分别有 26 例(51.0%)和 16 例(31.4%)观察到 OPN 表达和 S100A6 表达。更重要的是,通过免疫组织化学分析在任何非癌性肝标本中均未发现这些基因编码的蛋白质。这些基因的表达与低分化相关(OPN:P =.013;S100A6:P =.008)。
骨桥蛋白是一种分泌性磷酸蛋白,其在癌症的进展和转移中越来越受到关注,S100A6 是 S100 蛋白家族的成员,可发挥细胞增殖、分化、迁移和细胞骨架动力学的作用,可能是 HCC 有前途的诊断标志物和治疗靶点。此外,这些结果鼓励进一步研究这些蛋白质在癌症发展和进展中的作用。