CD133/EpCAM肿瘤干细胞标志物在结直肠癌细胞中的肿瘤分期研究

B. Milner, C. Penny, V. Gibbon, P. Kay, P. Ruff
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引用次数: 5

摘要

在实体肿瘤中,肿瘤相关的肿瘤干细胞(CSCs)被认为驱动和维持肿瘤的发展,并负责肿瘤复发。结直肠癌干细胞表达细胞特异性表面标志物,包括CD133、EpCAM、CD44、CD166和CD94f等。在本研究中,我们旨在对表达CSC标记物CD133和EpCAM的人结肠癌细胞系SW1116、HT29和DLD1的细胞群进行表征。这些细胞系分别代表结直肠肿瘤的早期、中期和晚期。采用流式细胞术对107个SW1116、HT29和DLD1细胞进行抗cd133和抗epcam联合染色。我们在此报告了在各自细胞系中共表达CD133/EpCAM表位的细胞比例的逐渐增加。SW1116细胞系中CD133+EpCAM+细胞占2.42±0.20%,HT29细胞系中CD133+EpCAM+细胞占5.13±0.17%,DLD1细胞系中CD133+EpCAM+细胞占10.30±0.2%。这些数据提示CD133/ EpCAM标记物表达频率可能与肿瘤分期和侵袭性有关。
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CD133/EpCAM Cancer Stem Cell Markers of Tumour Stage in Colorectal Cancer Cells
In solid tumours, a discreet population of tumour associated cancer stem cells (CSCs) are proposed to drive and sustain tumour development and be responsible for tumour relapse. Colorectal cancer stem cells express cellspecific surface markers, including amongst others, CD133, EpCAM, CD44, CD166, and CD94f. In the present study, we aimed to characterisecellpopulations in the human colon adenocarcinoma cell lines, SW1116, HT29 and DLD1, expressing both CSC markers CD133 and EpCAM. These cell lines represent early, mid and late stages of colorectal tumours, respectively. Up to 107 SW1116, HT29 and DLD1 cells, co-stained with anti-CD133 and anti-EpCAM, were evaluated using flow cytometry. We report here progressive increasing proportions of cells coexpressing the CD133/EpCAM epitopes in the respective cell lines. In the SW1116 cell line, 2.42 ± 0.20 percent of cells were CD133+EpCAM+, in the HT29 cell line, 5.13 ± 0.17 percent of cells were CD133+EpCAM+, and in the DLD1 cell line, 10.30 ± 0.2 percent of cells were CD133+EpCAM+. These data suggest the frequency of CD133/ EpCAM marker expression may be associated with tumour stage and aggression.
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