Ieta Keisuke, Tanaka Fumiaki, Haraguchi Naotsugu, Kita Yoshiaki, Sakashita Hiroyuki, Mimori Koshi, Matsumoto Toshifumi, Inoue Hiroshi, Kuwano Hiroyuki, Mori Masaki
Department of Surgery and Molecular Oncology, Medical Institute of Bioregulation, Kyushu University, 4546 Tsurumihara, Beppu 874-0838, Japan.
Ann Surg Oncol. 2008 Feb;15(2):638-48. doi: 10.1245/s10434-007-9605-3. Epub 2007 Oct 12.
Human prominin-1 (PROM1, CD133) was used as a marker to detect stem cells (progenitor cells) and cancer stem cells (tumor-initiating cells) in various tissues. The purpose of this study was to investigate the biological and genetic characteristics of tumor-initiating cells in colon cancer with both in vitro and in vivo analyses.
The CD133 expression of 12 colon cancer cell lines was evaluated. CD133+ cells were isolated by flow cytometry and examined for in vivo tumor formation, in vitro proliferation, colony formation, and invasion ability. Additionally, we used microarray analysis to compare gene expression profiles between CD133+ and CD133- isolated cells.
CD133+ cells were found in 5 of 12 colon cancer cell lines. Isolated CD133+ cells from the HT29 colon cancer cell line exhibited a higher tumorigenic potential than CD133- cells in the in vivo tumor formation assay. Furthermore, it was shown that CD133+ cells are more proliferative and have higher colony-forming and invasive abilities than CD133- cells in vitro. Microarray analysis found differential gene expression correlating with CD133 expression.
It was confirmed that CD133+ cells in colon cancer are useful markers for the detection of tumor-initiating cells. Intimate biological and genetic features of CD133+ cells in colon cancer cell lines were also revealed. The biological characteristics of CD133+ cells and differentially expressed genes in these cells will help elucidate more details of tumor-initiating cells in colon cancer.
人类prominin-1(PROM1,CD133)被用作检测各种组织中的干细胞(祖细胞)和癌症干细胞(肿瘤起始细胞)的标志物。本研究的目的是通过体外和体内分析来研究结肠癌中肿瘤起始细胞的生物学和遗传学特征。
评估了12种结肠癌细胞系的CD133表达。通过流式细胞术分离CD133+细胞,并检测其体内肿瘤形成、体外增殖、集落形成和侵袭能力。此外,我们使用微阵列分析比较了CD133+和CD133-分离细胞之间的基因表达谱。
在12种结肠癌细胞系中的5种中发现了CD133+细胞。在体内肿瘤形成试验中,从HT29结肠癌细胞系分离的CD133+细胞比CD133-细胞表现出更高的致瘤潜力。此外,结果表明,在体外CD133+细胞比CD133-细胞具有更强的增殖能力以及更高的集落形成和侵袭能力。微阵列分析发现与CD133表达相关的差异基因表达。
证实结肠癌中的CD133+细胞是检测肿瘤起始细胞的有用标志物。还揭示了结肠癌细胞系中CD133+细胞密切的生物学和遗传学特征。CD133+细胞的生物学特征以及这些细胞中差异表达的基因将有助于阐明结肠癌中肿瘤起始细胞的更多细节。