SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma

被引:24
作者
Deng, Gang [1 ]
Zhu, Lei [1 ]
Huang, Feizhou [1 ]
Nie, Wanpin [1 ]
Huang, Wei [1 ]
Xu, Hongbo [1 ]
Zheng, Shaopeng [1 ]
Yi, Zhongjie [1 ]
Wan, Tao [1 ]
机构
[1] Cent S Univ, Dept Hepatobiliary & Pancreat Surg, Xiangya Hosp 3, Changsha 410013, Hunan, Peoples R China
关键词
intrahepatic cholangiocarcinoma; SALL4; proliferation; migration; invasion; YOLK-SAC TUMORS; HEPATOCELLULAR-CARCINOMA; CELL MARKER; PROTEIN; 4; EXPRESSION; OVEREXPRESSION; BIOMARKER; STEMNESS; CANCERS;
D O I
10.18632/oncotarget.4862
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Intrahepatic cholangiocarcinoma (ICC) is the most common and deadly disease of the biliary tree due to its poor prognosis. Sal-like protein 4 (SALL4), a stem cell marker, has been identified as a potential target for aggressive hepatocellular carcinoma (HCC). In our study, 175 ICC cases with an average age of 55 years were included, and 53% (93/175) were male. And 28 adjacent non-tumor tissues were also collected. The SALL4-positive immunoreactivity was detected in a total of 102 ICC cases (58%), whereas all 28 adjacent tissues showed negative staining. Univariate analysis, showed that the SALL4-positive ICC cases had significantly more frequent lymph nodal metastasis (P = 0.0460), vascular invasion (P < 0.0001), and nerve invasion (P < 0.0001). Furthermore, the strong SALL4-positive cases (n = 7, 5 months) had shorter overall survival, when compared to moderate SALL4-positive (n = 46, 9 months) or SALL4- negative cases (n = 73, 7 months), respectively. Our data also suggest that SALL4 may be involved in the regulation of epithelial-mesenchymal transition (EMT) in ICC. Those results for the first time indicate an oncogenic role of SALL4 in ICC. Therefore, SALL4 may serve as a promising therapeutic target for ICC.
引用
收藏
页码:27416 / 27426
页数:11
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