CD44细胞
癌症干细胞
结直肠癌
癌症研究
克隆形成试验
干细胞
癌症
干细胞标记物
生物
上皮细胞粘附分子
体内
病理
医学
体外
内科学
细胞生物学
生物化学
生物技术
作者
Lixin Du,Hongyi Wang,Leya He,Jingyu Zhang,Biyun Ni,Xiaohui Wang,Haijing Jin,Nathalie Cahuzac,Maryam Mehrpour,Youyong Lü,Quan Chen
标识
DOI:10.1158/1078-0432.ccr-08-1034
摘要
Abstract Purpose: Both CD44 and CD133 were reported as putative markers for isolating colorectal cancer stem cells (CSC). It remains to be resolved if both of these markers are of functional importance for colorectal CSC. Experimental Design: The expression of CD44 and CD133 in normal colonic tissues and primary colorectal cancer was assessed by immunohistochemistry in a series of 60 patients on tissue microarray sections. Both in vitro clonogenic and in vivo tumorigenic assay were applied to measure CSC activities from the cells isolated from patients. Lentiviral RNA interference was used to stably knock down CD44 or CD133 in colorectal cancer cells from patients. Results: We found that CD44+ cells displayed clustered growth and they did not colocalize with CD133+ cells within colorectal cancer. As few as 100 CD44+ cells from a patients' tumor initiated a xenograft tumor in vivo. A single CD44+ cell from a tumor could form a sphere in vitro which has characteristic stem cell properties and was able to generate a xenograft tumor resembling the properties of the primary tumor. Knockdown of CD44, but not CD133, strongly prevented clonal formation and inhibited tumorigenicity in xenograft model. Conclusions: These results indicate that CD44 is a robust marker and is of functional importance for colorectal CSC for cancer initiation.
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