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脂肪酸辅酶A连接酶4在人类肝细胞癌中过度表达。

Fatty acid-CoA ligase 4 is overexpressed in human hepatocellular carcinoma.

作者信息

Sung Young Kwan, Hwang Sun Young, Park Mi Kyung, Bae Han Ik, Kim Woo Ho, Kim Jung-Chul, Kim Moonkyu

机构信息

Department of Immunology, Kyungpook National University Medical School and Hospital, Daegu, 700-422, Korea.

出版信息

Cancer Sci. 2003 May;94(5):421-4. doi: 10.1111/j.1349-7006.2003.tb01458.x.

Abstract

Fatty acid-CoA ligase 4 (FACL4) is a central enzyme controlling the unesterified arachidonic acid (AA) level in cells. It has been shown that FACL4 blocks apoptosis and promotes colon carcinogenesis by lowering the cellular level of unesterified AA. Consistent with this, FACL4 is upregulated in colon adenocarcinoma. The status of FACL4 in other tumors including hepatocellular carcinoma (HCC) is not known. Here, we report that FACL4 is overexpressed in human HCC compared with adjacent normal liver tissues. FACL4 mRNA and protein were overexpressed in 5 out of 12 (41.7%) and 3 out of 8 (37.5%) cases of HCC, respectively. Immunohistochemical staining showed strong fine granular intracytoplasmic staining in tumor cells, whereas we observed occasional weak staining in normal liver tissues surrounding the tumors. We found that 14 out of 37 (37.8%) HCC expressed moderate to strong FACL4 immunostaining. Both normal adult and fetal liver tissues showed very weak to no detectable staining, whereas 3 out of 10 (30%) cirrhotic livers expressed weak staining. In addition, we found that 4 out of 8 (50%) human hepatoma cell lines expressed high levels of FACL4 by northern blot analysis. Our results show that FACL4 is a new molecular marker for HCC and suggest that the FACL4 pathway may be involved in liver carcinogenesis.

摘要

脂肪酸辅酶A连接酶4(FACL4)是一种控制细胞内未酯化花生四烯酸(AA)水平的关键酶。研究表明,FACL4通过降低细胞内未酯化AA的水平来阻止细胞凋亡并促进结肠癌的发生。与此一致的是,FACL4在结肠腺癌中上调。FACL4在包括肝细胞癌(HCC)在内的其他肿瘤中的状态尚不清楚。在此,我们报告与相邻正常肝组织相比,FACL4在人类HCC中过表达。在12例HCC病例中的5例(41.7%)和8例中的3例(37.5%)中,FACL4 mRNA和蛋白分别过表达。免疫组织化学染色显示肿瘤细胞内有强烈的细颗粒状胞质染色,而在肿瘤周围的正常肝组织中我们偶尔观察到弱阳性染色。我们发现37例HCC中有14例(37.8%)表达中度至强的FACL4免疫染色。正常成人和胎儿肝组织显示非常弱至无可检测的染色,而10例肝硬化肝脏中有3例(30%)表达弱阳性染色。此外,通过Northern印迹分析我们发现8种人类肝癌细胞系中有4种(50%)表达高水平的FACL4。我们的结果表明FACL4是HCC的一种新的分子标志物,并提示FACL4途径可能参与肝癌的发生。

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