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Recognition and killing of cancer stem-like cell population in hepatocellular carcinoma cells by cytokine-induced killer cells via NKG2d-ligands recognition

机译:通过NKG2d-配体识别,细胞因子诱导的杀伤细胞识别和杀死肝癌细胞中的癌症干样细胞群

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摘要

There is an urgent need for more potent and safer approaches to eradicate cancer stem cells (CSCs) for curing cancer. In this study, we investigate cancer-killing activity (CKA) of cytokine-induced killer (CIK) cells against CSCs of hepatocellular carcinoma (HCC). To visualize CSCs in vitro by fluorescence imaging, and image and quantify CSCs in tumor xenograft-bearing mice by bioluminescence imaging, HCC cells were engineered with CSC detector vector encoding GFP and luciferase controlled by Nanog promoter. We found that CIK cells have a strong CKA in vitro against putative CSCs of HCC, as shown by tumorsphere formation and time-lapse imaging. Additionally, time-lapse recording firstly revealed that putative CSCs were attacked simultaneously by many CIK cells and finally eradicated by CIK cells, indicating the necessity of achieving sufficient effector-to-target ratios. We firstly illustrated that anti-NKG2D antibody blocking partially but significantly inhibited CKA of CIK cells against putative CSCs. More importantly, intravenous infusion of CIK cells remarkably delayed tumor growth in mice with a significant decrease in putative CSC number monitored by bioluminescence imaging. Taken together, these findings demonstrate CKA of CIK cells against putative CSCs of HCC, at least in part, by NKG2D-ligands recognition.
机译:迫切需要更有效,更安全的方法来根除癌症干细胞(CSC)以治愈癌症。在这项研究中,我们调查了针对肝细胞癌(HCC)CSC的细胞因子诱导的杀伤(CIK)细胞的杀癌活性(CKA)。为了通过荧光成像在体外观察CSC,并通过生物发光成像对荷瘤异种移植小鼠中的CSC进行成像和定量,将HCC细胞用编码GFP的CSC检测器载体和由Nanog启动子控制的荧光素酶进行工程改造。我们发现,CIK细胞在体外具有抗HCC假定的CSC的强大CKA,如肿瘤球形成和延时成像所示。另外,延时记录首先显示推定的CSC同时受到许多CIK细胞的攻击,最后被CIK细胞根除,这表明有必要实现足够的效应子与靶标比率。我们首先说明抗NKG2D抗体部分阻断但显着抑制CIK细胞对假定的CSC的CKA。更重要的是,CIK细胞的静脉输注显着延迟了小鼠的肿瘤生长,并通过生物发光成像监测了推定的CSC数量显着下降。综上所述,这些发现至少部分地通过NKG2D-配体识别证明了CIK细胞针对HCC的假定CSC的CKA。

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