Expression of stemness markers ( CD133 and EpCAM) in prognostication of hepatocellular carcinoma

被引:81
作者
Chan, Anthony W. H. [1 ]
Tong, Joanna H. M. [1 ,2 ,3 ]
Chan, Stephen L. [4 ]
Lai, Paul B. S. [5 ]
To, Ka-Fai [1 ,2 ,3 ]
机构
[1] Chinese Univ Hong Kong, Dept Anat & Cellular Pathol, Prince Wales Hosp, State Key Lab Oncol South China, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Inst Digest Dis, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Sir YK Pao Canc Ctr, Shatin, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Dept Clin Oncol, Prince Wales Hosp, State Key Lab Oncol South China, Shatin, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Dept Surg, Div Hepatobiliary & Pancreat Surg, Shatin, Hong Kong, Peoples R China
关键词
AJCC TNM stage; CD133; EpCAM; hepatocellular carcinoma; stemness marker; CELL ADHESION MOLECULE; POOR-PROGNOSIS; STEM/PROGENITOR CELLS; TUMOR-CELLS; SURVIVAL;
D O I
10.1111/his.12342
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
AimsThe expression of stemness markers in hepatocellular carcinoma (HCC) is suggested to be associated with poor clinical outcome after surgical resection. There are few data on their independent prognostic role in addition to the existing AJCC TNM staging system. Methods and resultsThe immunohistochemical expression of CD133, EpCAM, CK19 and CD56 was studied in a cohort of 282 surgical specimens collected from patients undergoing resection of primary HCC. CD133-positive HCCs were usually smaller in size (P=0.002) and arose more frequently in cirrhotic liver (P=0.002). CD133 expression was an independent prognostic factor for overall survival (hazard ratio 2.30, P<0.001), and a highly potent prognostic factor in patients with stage I disease (hazard ratio 3.91, P=0.001). EpCAM expression was associated with younger age (P<0.001), smaller tumour size (P=0.018) and poorer histological differentiation (P=0.042). EpCAM immunoreactivity was an independent factor for disease-free survival in HCCs at all stages (hazard ratio 2.05, P=0.001), stage II (hazard ratio 3.66, P=0.010) and stages III/IV (hazard ratio 3.22, P=0.001). Neither CK19 nor CD56 offered any independent prognostic value. ConclusionThe prognostic role of CD133 was most significant in TNM stage I disease, while the prognostic role of EpCAM was more apparent in more advanced TNM stages.
引用
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页码:935 / 950
页数:16
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