Department Pathology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Department Pathology, Teikyo University School of Medicine, Tokyo, Japan.
Cancer Sci. 2020 Jul;111(7):2598-2607. doi: 10.1111/cas.14435. Epub 2020 May 20.
Cancer stem cells (CSCs) play a decisive role in the development and progression of cancer. To investigate CSCs in Epstein-Barr virus (EBV)-associated carcinoma (EBVaGC), we screened previously reported stem cell markers of gastric cancer in EBV-infected gastric cancer cell lines (TMK1 and NUGC3) and identified CD44v6v9 double positive cells as candidate CSCs. CD44v6/v9 cells were sorted from EBVaGC cell line (SNU719) cells and EBV-infected TMK1 cells and these cell populations showed high spheroid-forming ability and tumor formation in SCID mice compared with the respective CD44v6/v9 cells. Sphere-forming ability was dependent on the nuclear factor-κB (NF-κB) signaling pathway, which was confirmed by decrease of sphere formation ability under BAY 11-7082. Small interfering RNA knockdown of latent membrane protein 2A (LMP2A), one of the latent gene products of EBV infection, decreased spheroid formation in SNU719 cells. Transfection of the LMP2A gene increased the sphere-forming ability of TMK1 cells, which was mediated through NF-κB signaling. Together, these results indicate that CD44v6v9 cells are CSCs in EBVaGC that are maintained through the LMP2A/NF-κB pathway. Future studies should investigate CD44v6/v9 cells in normal and neoplastic gastric epithelium to prevent and treat this specific subtype of gastric cancer infected with EBV.
癌症干细胞(CSCs)在癌症的发生和发展中起着决定性作用。为了研究 EBV 相关癌(EBVaGC)中的 CSCs,我们筛选了先前报道的胃癌干细胞标志物在 EBV 感染的胃癌细胞系(TMK1 和 NUGC3)中的表达情况,并鉴定出 CD44v6v9 双阳性细胞作为候选 CSCs。我们从 EBVaGC 细胞系(SNU719)和 EBV 感染的 TMK1 细胞中分离出 CD44v6/v9 细胞,与相应的 CD44v6/v9 细胞相比,这些细胞群体具有较高的球体形成能力和在 SCID 小鼠中的肿瘤形成能力。球体形成能力依赖于核因子-κB(NF-κB)信号通路,这一点通过 BAY 11-7082 降低球体形成能力得到了证实。潜伏膜蛋白 2A(LMP2A)是 EBV 感染的潜伏基因产物之一,其小干扰 RNA 敲低降低了 SNU719 细胞的球体形成能力。LMP2A 基因的转染增加了 TMK1 细胞的球体形成能力,这是通过 NF-κB 信号介导的。总之,这些结果表明 CD44v6v9 细胞是 EBVaGC 中的 CSCs,通过 LMP2A/NF-κB 通路维持。未来的研究应该在正常和肿瘤性胃上皮中研究 CD44v6/v9 细胞,以预防和治疗这种特定亚型的感染 EBV 的胃癌。