Thoracic and GI Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20814, USA.
Experimental Transplantation and Immunology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Stem Cell Rev Rep. 2023 Aug;19(6):2013-2023. doi: 10.1007/s12015-023-10557-7. Epub 2023 May 30.
Cholangiocarcinoma is an aggressive type of liver cancer with few effective treatment options. Therefore, there is great need to better understand the biology of this malignancy to further development of novel treatment options. Cancer stem cells (CSCs) are thought to the underlying reason for cancer initiation, metastasis, and relapse. However, due to their elusive character and differences in identification among different types of cancer, it remains a challenge to study such cells. Additionally, characterization of the tumor microenvironment such as interactions with immune cells remain largely unknown. Here, we employ a fluorescent reporter system to track and isolate stem-like cancer cells of cholangiocarcinoma cell lines. Following verification of a stem-like signature (upregulated expression of stemness markers, resistance to chemotherapy, increased spheroid formation, and tumorigenesis capabilities despite inoculation of a small number of cells), we analyzed the interaction of these cells with macrophages via direct and indirect coculture assays. We noted direct coculturing increased stemness among CSC populations and induced both M1 (CD80 and HLA-DR) and M2 (CD163) tumor associated macrophage polarization. These studies suggest that there is a bi-directional crosstalk between macrophages and CSCs that promotes stemness renewal and tumor associated macrophage polarization.
胆管癌是一种侵袭性肝癌,治疗选择有限。因此,非常有必要更好地了解这种恶性肿瘤的生物学特性,以进一步开发新的治疗方法。癌症干细胞(CSCs)被认为是癌症发生、转移和复发的根本原因。然而,由于其难以捉摸的特性以及不同类型癌症之间鉴定的差异,研究这些细胞仍然是一个挑战。此外,肿瘤微环境的特征,如与免疫细胞的相互作用,在很大程度上仍然未知。在这里,我们采用荧光报告系统来跟踪和分离胆管癌细胞系中的类干细胞样癌症细胞。在验证了类干细胞特征(干性标志物的上调表达、对化疗的耐药性、增加球体形成和肿瘤发生能力,尽管接种的细胞数量很少)之后,我们通过直接和间接共培养分析了这些细胞与巨噬细胞的相互作用。我们注意到直接共培养增加了 CSC 群体中的干性,并诱导了 M1(CD80 和 HLA-DR)和 M2(CD163)肿瘤相关巨噬细胞极化。这些研究表明,巨噬细胞和 CSCs 之间存在双向的串扰,促进了干性更新和肿瘤相关巨噬细胞极化。