Prognostic impact of the expression of putative cancer stem cell markers CD133, CD166, CD44s, EpCAM, and ALDH1 in colorectal cancer

被引:252
作者
Lugli, A. [1 ]
Iezzi, G. [2 ]
Hostettler, I. [1 ]
Muraro, M. G. [2 ]
Mele, V. [1 ,2 ]
Tornillo, L. [1 ]
Carafa, V. [1 ]
Spagnoli, G. [2 ]
Terracciano, L. [1 ]
Zlobec, I. [1 ]
机构
[1] Univ Basel, Inst Pathol, Basel, Switzerland
[2] Univ Basel, Inst Surg Res & Hosp Management, Basel, Switzerland
关键词
colorectal cancer; cancer stem cell; CD44; CD166; CD133; EpCAM; ADHESION MOLECULE; COLON-CANCER; CARCINOMA PATIENTS; TUMOR PROGRESSION; BREAST-CANCER; EP-CAM; SURVIVAL; ALCAM/CD166; METASTASIS; PREDICTOR;
D O I
10.1038/sj.bjc.6605762
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: The aim of this study was to elucidate the prognostic impact of putative cancer stem cell markers CD133, CD166, CD44s, EpCAM, and aldehyde dehydrogenase-1 (ALDH1) in colorectal cancer. METHODS: A tissue microarray of 1420 primary colorectal cancers and 57 normal mucosa samples was immunostained for CD133, CD166, CD44s, EpCAM, and ALDH1 in addition to 101 corresponding whole tissue sections. Invasive potential of three colorectal cancer cell lines was tested. RESULTS: Differences between normal tissue and cancer were observed for all markers (P<0.001). Loss of membranous CD166 and CD44s were linked to higher pT (P = 0.002, P = 0.014), pN (P = 0.004, P = 0.002), an infiltrating growth pattern (P<0.001, P = 0.002), and worse survival (P = 0.015, P = 0.019) in univariate analysis only. Loss of membranous EpCAM expression was also linked to higher pN (P = 0.023) and infiltrating growth pattern (P = 0.005). The CD44s, CD166, and EpCAM expression were lost towards the invasive front. The CD44-/CD166- cells from three colorectal cancer cell lines exhibited significantly higher invasive potential in vitro than their positive counterparts. CONCLUSIONS: Loss, rather than overexpression, of membranous CD44s, CD166, and EpCAM is linked to tumour progression. This supports the notion that the membranous evaluation of these proteins assessed by immunohistochemistry may be representative of their cell adhesion rather than their intra-cellular functions. British Journal of Cancer (2010) 103, 382-390. doi:10.1038/sj.bjc.6605762 www.bjcancer.com Published online 6 July 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:382 / 390
页数:9
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