Department of Pathology, Chang Bing Show Chwan Memorial Hospital, Changhua County 505, Taiwan.
Center for General Education, Providence University, Taichung City 433, Taiwan.
Int J Med Sci. 2018 Nov 23;15(14):1746-1756. doi: 10.7150/ijms.28440. eCollection 2018.
We previously reported that modulation of cytokeratin18 induces pleomorphism of liver cells, higher cell motility, and higher drug sensitivity to sorafenib treatment of hepatoma cells. These relationships were established by experiments. The aim of this study was to determine the association between cytokeratin expression and tumor behavior, as well as cancer stem cells of hepatocellular carcinoma and intra-hepatic cholangiocarcinoma in Taiwan. Cytokeratins and sal-like protein 4 expression was determined in 83 hepatocellular carcinoma and 30 intra-hepatic cholangiocarcinoma specimens by immunohistochemistry. The relationship between cytokeratins and sal-like protein 4 expression with hepatitis virus infection, clinicopathologic factors, and survival was analyzed. Further, the correlation among cytokeratins and sal-like protein 4 expression was studied. In addition to cytokeratin8/18, the expression of cytokeratin7/19 and sal-like protein 4 was noted in hepatocellular carcinoma; however, only cytokeratin19 expression had a significant correlation with poor overall survival and poor disease-free survival. The expression of cytokeratins and sal-like protein 4 was not correlated with hepatitis virus infection. The expression of cytokeratin19, but not 7, 8, and 18, was correlated with sal-like protein 4 expression in hepatocellular carcinoma. Cytokeratin7 expression was decreased and the sal-like protein 4 expression was absent in all 30 intra-hepatic cholangiocarcinoma cases. The expression of cytokeratins had not statistically significant correlation with overall and disease-free survival in patients with intra-hepatic cholangiocarcinoma. The expression of cytokeratin19 was associated with sal-like protein 4 expression, as well as poor overall and disease-free survival in hepatocellular carcinoma patients in Taiwan.
我们之前的研究报道,细胞角蛋白 18 的调节可诱导肝细胞的多形性、更高的细胞迁移能力以及索拉非尼治疗肝癌细胞的药物敏感性更高。这些关系是通过实验建立的。本研究的目的是确定细胞角蛋白表达与肝癌和肝内胆管细胞癌在台湾的肿瘤行为以及癌症干细胞之间的关系。通过免疫组织化学方法检测 83 例肝细胞癌和 30 例肝内胆管细胞癌标本中细胞角蛋白和 SALL4 的表达。分析细胞角蛋白和 SALL4 表达与肝炎病毒感染、临床病理因素和生存的关系。进一步研究细胞角蛋白和 SALL4 表达之间的相关性。除了细胞角蛋白 8/18,在肝细胞癌中还观察到细胞角蛋白 7/19 和 SALL4 的表达;然而,只有细胞角蛋白 19 的表达与总生存和无病生存不良显著相关。细胞角蛋白和 SALL4 的表达与肝炎病毒感染无关。在肝细胞癌中,细胞角蛋白 19 的表达与 SALL4 表达相关,但细胞角蛋白 7、8 和 18 的表达与 SALL4 表达无关。在所有 30 例肝内胆管细胞癌中,细胞角蛋白 7 的表达减少,SALL4 的表达缺失。细胞角蛋白在肝内胆管细胞癌患者中的表达与总生存和无病生存无统计学显著相关性。在台湾的肝细胞癌患者中,细胞角蛋白 19 的表达与 SALL4 表达以及总生存和无病生存不良相关。