Division of Gastroenterology and Hepatology, Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.
Hepatology. 2013 Apr;57(4):1469-83. doi: 10.1002/hep.26159. Epub 2013 Mar 6.
Liver cancers, including hepatocellular carcinomas (HCCs), cholangiocarcinomas (CCs), and fibrolamellar HCCs (FL-HCCs) are among the most common cancers worldwide and are associated with a poor prognosis. Investigations of genes important in liver cancers have focused on Sal-like protein 4 (SALL4), a member of a family of zinc finger transcription factors. It is a regulator of embryogenesis, organogenesis, pluripotency, can elicit reprogramming of somatic cells, and is a marker of stem cells. We found it expressed in normal murine hepatoblasts, normal human hepatic stem cells, hepatoblasts and biliary tree stem cells, but not in mature parenchymal cells of liver or biliary tree. It was strongly expressed in surgical specimens of human HCCs, CCs, a combined hepatocellular and cholangiocarcinoma, a FL-HCC, and in derivative, transplantable tumor lines in immune-compromised hosts. Bioinformatics analyses indicated that elevated expression of SALL4 in tumors is associated with poor survival of HCC patients. Experimental manipulation of SALL4's expression results in changes in proliferation versus differentiation in human HCC cell lines in vitro and in vivo in immune-compromised hosts. Virus-mediated gene transfer of SALL4 was used for gain- and loss-of-function analyses in the cell lines. Significant growth inhibition in vitro and in vivo, accompanied by an increase in differentiation occurred with down-regulation of SALL4. Overexpression of SALL4 resulted in increased cell proliferation in vitro, correlating with an increase in expression of cytokeratin19 (CK19), epithelial cell adhesion molecules (EpCAM), and adenosine triphosphate (ATP)-binding cassette-G2 (ABCG2).
SALL4's expression is an indicator of stem cells, a prognostic marker in liver cancers, correlates with cell and tumor growth, with resistance to 5-FU, and its suppression results in differentiation and slowed tumor growth. SALL4 is a novel therapeutic target for liver cancers.
肝脏癌症,包括肝细胞癌(HCCs)、胆管癌(CCs)和纤维板层 HCC(FL-HCC),是全球最常见的癌症之一,预后不良。对肝脏癌症中重要基因的研究集中在 Sall 样蛋白 4(SALL4)上,它是锌指转录因子家族的一员。它是胚胎发生、器官发生、多能性的调节剂,可以引起体细胞的重编程,并且是干细胞的标志物。我们发现它在正常的鼠肝母细胞、正常的人肝干细胞、肝母细胞和胆管树干细胞中表达,但不在成熟的肝实质细胞或胆管树中表达。它在人 HCCs、CCs、肝细胞癌和胆管癌的联合肿瘤、FL-HCC 的手术标本中以及在免疫缺陷宿主中的可移植肿瘤系中强烈表达。生物信息学分析表明,SALL4 在肿瘤中的高表达与 HCC 患者的生存率差有关。SALL4 表达的实验操作导致体外 HCC 细胞系的增殖与分化发生变化,并在免疫缺陷宿主中发生体内变化。病毒介导的 SALL4 基因转移用于细胞系中的功能获得和功能丧失分析。下调 SALL4 可显著抑制体外和体内的生长,同时增加分化。SALL4 的过表达导致体外细胞增殖增加,与细胞角蛋白 19(CK19)、上皮细胞黏附分子(EpCAM)和三磷酸腺苷(ATP)结合盒-G2(ABCG2)的表达增加相关。
SALL4 的表达是干细胞的标志物,是肝脏癌症的预后标志物,与细胞和肿瘤生长相关,与 5-FU 耐药相关,其抑制导致分化和肿瘤生长减缓。SALL4 是肝脏癌症的新治疗靶点。