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结直肠癌细胞的特征:一种以 CD133 为潜在干细胞标志物的功能方法。

Characterization of colon cancer cells: a functional approach characterizing CD133 as a potential stem cell marker.

机构信息

Department of Urology, University of Heidelberg, Im Neuenheimer Feld 110, D-69120 Heidelberg, Germany.

出版信息

BMC Cancer. 2012 Mar 20;12:96. doi: 10.1186/1471-2407-12-96.

Abstract

BACKGROUND

Isolation and characterization of tumourigenic colon cancer initiating cells may help to develop novel diagnostic and therapeutic procedures.

METHODS

We characterized a panel of fourteen human colon carcinoma cell lines and their corresponding xenografts for the surface expression of potential stem cell markers CD133, CD24, CD44, CDCP1 and CXCR4. In five cell lines and nine xenografts, mRNA expression of these markers was determined. Tumour growth behaviour of CD133+, CD133- and unsorted SW620 cells was evaluated in vivo.

RESULTS

All five putative stem cell markers showed distinct expression patterns in the tumours examined. Two patient-derived cell lines highly expressed CD133 (> 85% of positive cells) and three other cell lines had an expression level of about 50% whereas in long-term culture based models CD133 expression ranged only from 0 to 20%. In 8/14 cell lines, more than 80% of the cells were positive for CD24 and 11/14 were over 70% positive for CD44. 10/14 cell lines expressed CDCP1 on ≥ 83% of cells. CXCR4 expression was determined solely on 94 L and SW480.Analyses of the corresponding xenografts revealed a significant reduction of cell numbers expressing the investigated surface markers and showed single cell fractions expressing up to three markers simultaneously.Statistical analysis revealed that the CXCR4 mRNA level correlates negatively with the protein expression of CD133, CD44, CD24 and CDCP1 in cell lines and xenografts.A lower differentiation grade of donor material correlated with a higher CDCP1 mRNA expression level in the respective tumour model.In vivo growth behaviour studies of SW620 revealed significantly higher take rates and shorter doubling times in the tumour growth of CD133 positive subclones in comparison to the unsorted cell line or CD133 negative subclones.

CONCLUSIONS

Our data revealed correlations in the expression of surface markers CD44 and CD24 as well as CD44 and CDCP1 and strongly suggest that CD133 is a stem cell marker within our colon carcinoma panel. Further studies will elucidate its role as a potential therapeutic target.

摘要

背景

分离和鉴定肿瘤起始细胞有助于开发新的诊断和治疗方法。

方法

我们对十四个人结肠癌细胞系及其相应的异种移植瘤进行了表面表达潜在干细胞标志物 CD133、CD24、CD44、CDCP1 和 CXCR4 的鉴定。在五个细胞系和九个异种移植瘤中,测定了这些标志物的 mRNA 表达。在体内评估了 CD133+、CD133-和未分选的 SW620 细胞的肿瘤生长行为。

结果

在检查的肿瘤中,所有五个假定的干细胞标志物均表现出不同的表达模式。两个患者来源的细胞系高度表达 CD133(>85%的阳性细胞),另外三个细胞系的表达水平约为 50%,而在长期培养的模型中,CD133 的表达范围仅为 0 至 20%。在 14 个细胞系中的 8 个中,超过 80%的细胞对 CD24 呈阳性,14 个中有 11 个对 CD44 呈阳性超过 70%。14 个细胞系中有 10 个对 CDCP1 的表达超过 83%。仅在 94 L 和 SW480 上检测到 CXCR4 的表达。相应异种移植瘤的分析显示,表达所研究表面标志物的细胞数量显著减少,并显示出单个细胞分数同时表达多达三个标志物。统计分析显示,细胞系和异种移植瘤中 CXCR4 mRNA 水平与 CD133、CD44、CD24 和 CDCP1 的蛋白表达呈负相关。供体材料的分化程度较低与相应肿瘤模型中 CDCP1 mRNA 表达水平较高相关。SW620 的体内生长行为研究表明,与未分选的细胞系或 CD133 阴性亚克隆相比,CD133 阳性亚克隆在肿瘤生长中的接种率显著更高,倍增时间更短。

结论

我们的数据显示 CD44 和 CD24 以及 CD44 和 CDCP1 的表达存在相关性,并强烈表明 CD133 是我们结肠癌细胞系中的干细胞标志物。进一步的研究将阐明其作为潜在治疗靶点的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7caa/3368744/06684eebee8b/1471-2407-12-96-1.jpg

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