Experimental Tumor Pathology, Institute of Pathology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
Institute of Pathology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
J Cell Mol Med. 2018 Dec;22(12):6238-6248. doi: 10.1111/jcmm.13911. Epub 2018 Oct 2.
Hepatocellular carcinoma (HCC) is one of the most common causes for cancer-related death worldwide with rapidly increasing incidence and mortality rates. As for other types of cancers, also in HCC cancer stem cells (CSCs) are thought to be responsible for tumour initiation, progression and therapy failure. However, as rare subpopulations of tumour tissue, CSCs are difficult to isolate, thus making the development of suitable and reliable model systems necessary. In our study, we generated HepG2 subclones with enriched CSC potential by application of the spheroid formation method and subsequent single-cell cloning. Analyses in several 2D and 3D cell culture systems as well as a panel of functional assays both in vitro and in vivo revealed that the generated subclones displayed characteristic and sustained features of tumour initiating cells as well as highly aggressive properties related to tumour progression and metastasis. These characteristics could clearly be correlated with the expression of CSC markers that might have prognostic value in the clinical HCC setting. Therefore, we conclude that our CSC enriched HepG2 clones certainly represent suitable model systems to study the role of CSCs during HCC initiation, progression and drug resistance.
肝细胞癌 (HCC) 是全球癌症相关死亡的最常见原因之一,其发病率和死亡率迅速上升。与其他类型的癌症一样,在 HCC 中,癌症干细胞 (CSC) 被认为是肿瘤发生、进展和治疗失败的原因。然而,作为肿瘤组织中的罕见亚群,CSC 难以分离,因此需要开发合适和可靠的模型系统。在我们的研究中,我们通过应用球体形成方法和随后的单细胞克隆,生成了具有富集 CSC 潜力的 HepG2 亚克隆。在几种 2D 和 3D 细胞培养系统以及一系列体外和体内功能测定中进行的分析表明,所生成的亚克隆表现出肿瘤起始细胞的特征和持续特征,以及与肿瘤进展和转移相关的高度侵袭性特性。这些特征可以与 CSC 标志物的表达清楚地相关联,这些标志物在 HCC 的临床环境中可能具有预后价值。因此,我们得出结论,我们富含 CSC 的 HepG2 克隆肯定代表了合适的模型系统,可以研究 CSC 在 HCC 起始、进展和耐药性过程中的作用。