Benayoun Liat, Shaked Yuval
Department of Molecular Pharmacology, Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Curr Protoc Stem Cell Biol. 2013 Feb;Chapter 3:Unit 3.7. doi: 10.1002/9780470151808.sc0307s24.
This unit describes protocols for culturing and subsequently enriching cancer stem cells (CSCs), also referred to as tumor-initiating cells (TICs), from human established cell lines. TICs are thought to display the major cell population in the tumor with the proliferative capacity to seed tumors, implying that they( )are critical in initiating and driving tumorigenesis. The protocols show the methods for enriching and subsequently characterizing TIC populations from a series of human tumors including glioblastoma, breast, and pancreatic tumors. Protocols evaluating the morphology, phenotypic, and functional properties of TICs are described. Long-term cultures grown either as monolayers ("TIC-low") or as non-adherent tumor spheres ("TIC-high") are generated. As a result, cells from the TIC-high culture exhibit increased expression of stem cell surface markers, such as CD133, CD44, and CD24, high aldehyde dehydrogenase (ALDH) activity, and elevated expression levels of p21, in comparison to cells from the TIC-low culture. Studying TICs by using such protocols is cost effective and is considered as a suitable and simple way for studying them.
本单元介绍了从人源已建细胞系中培养并随后富集癌症干细胞(CSCs)(也称为肿瘤起始细胞(TICs))的实验方案。人们认为TICs是肿瘤中的主要细胞群体,具有播种肿瘤的增殖能力,这意味着它们在启动和驱动肿瘤发生过程中至关重要。这些实验方案展示了从一系列人类肿瘤(包括胶质母细胞瘤、乳腺癌和胰腺肿瘤)中富集并随后鉴定TIC群体的方法。描述了评估TICs形态、表型和功能特性的实验方案。生成了以单层培养(“低TIC”)或非贴壁肿瘤球(“高TIC”)形式生长的长期培养物。结果,与低TIC培养物中的细胞相比,高TIC培养物中的细胞表现出干细胞表面标志物(如CD133、CD44和CD24)表达增加、高醛脱氢酶(ALDH)活性以及p21表达水平升高。使用此类实验方案研究TICs具有成本效益,被认为是研究它们的一种合适且简单的方法。