Department of Clinical Biochemistry, Chinese PLA General Hospital, Beijing, People's Republic of China.
Cell Biol Int. 2012 Sep;36(9):803-9. doi: 10.1042/CBI20100920.
HCC (hepatocellular carcinoma) is often diagnosed at an advanced stage with poor prognosis. Peripheral blood may be useful in cancer classification, and therefore we investigated the gene expression found by Affymetrix HG-U133 Plus2.0 microarray, with samples from nine HCC patients and five healthy NC (normal controls). A total of 726 probe sets showed significant differences based on the criteria of P<0.05 and absolute fold change >2. The genes were related to many biological functions, including immune response, transcription regulation and metabolism processes. Ten genes [IL-8 (interleukin 8), GOS2 (G0 /G1 switch gene 2), CXCR4 (CXC chemokine receptor 4), FOS, RPS24 (40S ribosomal protein S24), HAP90AA1, PFDN5, RPL27, GZMA and PFN1] showing significant differences were confirmed by real-time PCR in 54 HCC patients and 56 healthy NC. Seven genes [IL-8, GOS2, CXCR4, FOS, RPS24, HSP90AA1 (heat shock protein 90AA1) and PFN1] showed significant difference both in RT-PCR (reverse transcription-PCR) and microarray. Expression of IL-8 and FOS proteins was up-regulated in HCC compared with healthy controls. A gene signature in peripheral blood which can distinguish HCC patients and healthy controls may have been identified.
HCC(肝细胞癌)通常在晚期诊断,预后不良。外周血可能有助于癌症分类,因此我们研究了 Affymetrix HG-U133 Plus2.0 微阵列发现的基因表达,样本来自 9 名 HCC 患者和 5 名健康 NC(正常对照)。根据 P<0.05 和绝对倍数变化>2 的标准,共有 726 个探针集显示出显著差异。这些基因与许多生物学功能有关,包括免疫反应、转录调控和代谢过程。通过实时 PCR 在 54 名 HCC 患者和 56 名健康 NC 中验证了 10 个差异显著的基因[白细胞介素 8 (IL-8)、G0 / G1 开关基因 2 (GOS2)、CXC 趋化因子受体 4 (CXCR4)、FOS、40S 核糖体蛋白 S24 (RPS24)、HAP90AA1、PFDN5、RPL27、GZMA 和 PFN1]。7 个基因[白细胞介素 8、G0 / G1 开关基因 2、CXC 趋化因子受体 4、FOS、RPS24、热休克蛋白 90AA1 (HSP90AA1) 和 PFN1]在 RT-PCR(逆转录-PCR)和微阵列中均显示出显著差异。与健康对照组相比,HCC 中 IL-8 和 FOS 蛋白的表达上调。在外周血中可以区分 HCC 患者和健康对照者的基因特征可能已经确定。