Molecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia ; Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Molecular Pathology Unit, Cancer Research Centre, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia.
Cancer Cell Int. 2014 Oct 9;14(1):101. doi: 10.1186/s12935-014-0101-0. eCollection 2014.
Side population (SP) assay identifies cells with dye/drug extrusion ability, a characteristic of stem cells. Here, we determined if SP cells exist in a verified cell line originating from recurrent nasopharyngeal carcinoma (NPC) and a xenograft established from recurrent metastatic NPC. These cells were evaluated for stem-like properties via functional assays as well as for tumourigenicity.
We used Hoechst 33342 to identify the SP from non-SP (NSP) cells in HK1 NPC cell line and xeno-284 NPC xenograft. The cells were assayed for in vitro characteristics of cancer stem cells (CSC), gene expression and tumourigenicity ability. Student's t test was used to test for significance.
Five to ten percent and less than 0.5% of HK1 and xeno-284 NPC cells, respectively, were SP cells. Fumitremorgin C (FTC), as opposed to verapamil, was effective in causing the cells to retain Hoechst 33342 dye. HK1 SP cells formed more holoclones, had more aldehyde dehydrogenase (ALDH) activity, divided asymmetrically and contained slow-proliferating cells. ABCG2, SOX2, TERT, MYC, Hedgehog, Notch, TGFβ and Wnt signalling pathway genes were significantly upregulated in the SP cells. However, despite these differences in vitro, both HK1 SP and NSP cells had an overall similar tumourigenic potential in vivo.
HK1 SP cells were ABCG2-specific as confirmed by FTC inhibition and gene expression data. Despite data from in vitro and gene expression experiments suggesting stem-like features, there was no significant difference in tumourigenic potential between SP and NSP cells. We conclude that SP assay alone is not sufficient to identify CSCs in HK1 cells. Our work also suggests the presence of a stem-cell like population among NPC cells which do not display increased tumourigenicity.
侧群(SP)分析鉴定具有染料/药物外排能力的细胞,这是干细胞的特征。在这里,我们确定是否存在于源自复发性鼻咽癌(NPC)的已验证细胞系和源自复发性转移性 NPC 的异种移植物中的 SP 细胞。通过功能测定以及致瘤性评估,这些细胞被评估为具有类干细胞特性。
我们使用 Hoechst 33342 来鉴定 HK1 NPC 细胞系和 xeno-284 NPC 异种移植物中的 SP 细胞和非 SP(NSP)细胞。对这些细胞进行体外癌症干细胞(CSC)特性分析、基因表达和致瘤能力检测。使用 Student's t 检验来检验显著性。
HK1 和 xeno-284 NPC 细胞中分别有 5-10%和小于 0.5%的细胞为 SP 细胞。与维拉帕米相反,Fumitremorgin C(FTC)可有效地使细胞保留 Hoechst 33342 染料。HK1 SP 细胞形成更多的全克隆,具有更高的醛脱氢酶(ALDH)活性,不对称分裂并含有增殖缓慢的细胞。ABC-G2、SOX2、TERT、MYC、Hedgehog、Notch、TGFβ和 Wnt 信号通路基因在 SP 细胞中显著上调。然而,尽管在体外存在这些差异,但 HK1 SP 和 NSP 细胞在体内具有总体相似的致瘤潜能。
通过 FTC 抑制和基因表达数据证实,HK1 SP 细胞为 ABCG2 特异性。尽管来自体外和基因表达实验的数据表明具有干细胞样特征,但 SP 和 NSP 细胞之间的致瘤潜能没有显著差异。我们得出结论,单独的 SP 分析不足以鉴定 HK1 细胞中的 CSCs。我们的工作还表明,NPC 细胞中存在具有干细胞样特征的群体,而这些细胞并不显示出增加的致瘤性。