RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Antileukemia Activity of Human Natural Killer Cell-Derived Nanomagic Bullets against Acute Myeloid Leukemia (AML).
Antileukemia Activity of Human Natural Killer Cell-Derived Nanomagic Bullets against Acute Myeloid Leukemia (AML).
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癌症是医学领域面临的严重健康问题之一,治疗通常需要采取强效措施,但患者预后仍然较差。应用 NK 细胞来源外泌体(NK-Exo)是癌症免疫治疗的一种新方法。这些直径为 30–120 nm 的纳米颗粒是母细胞的微型载体。本研究在体外考察 NK-Exo 和 LAK-Exo(活化 NK 细胞来源外泌体)对急性髓系白血病(AML)的抗肿瘤活性。
采用 MACS 方法从健康供者白膜层中分离 NK 细胞,并使用 EXOCIBE 试剂盒分离 NK-Exo。以不同剂量 NK-Exo 处理 KG-1 细胞系后,分别采用 MTT 检测和 Annexin V-PE 测定评估细胞增殖和凋亡;通过实时 PCR 和蛋白质印迹确认相关蛋白。
NK-Exo 和 LAK-Exo 的抗肿瘤活性呈剂量和时间依赖性。孵育 48 小时并使用 50 μg/mL 外泌体时,活性最高(p<0.0001)。然而,较低浓度 NK-Exo(p<0.05)和 LAK-Exo(p<0.001)在较短时间内也能产生细胞毒作用。LAK-Exo 对靶细胞的细胞毒作用显著强于 NK-Exo。不同凋亡通路的诱导具有时间点依赖性。肿瘤细胞与 50 μg/mL NK-Exo 或 LAK-Exo 共培养 48 小时后,总凋亡率分别为 34.56% 和 51.6%。50 μg/mL NK-Exo 和 LAK-Exo 处理细胞中 CASPASE3、P38 和 CYTOCHROME C 基因表达显著。本研究证实 NK-Exo 在体外具有抗 AML 肿瘤细胞活性。因此,NK-Exo 可作为白血病治疗中有前景且有效的方法。
Background: Cancer is among the serious health problems of the medical world, for treatment of which severe treatments are used.
However, the prognosis of cancer patients is still poor. The application of NK cell-derived exosomes (NK-Exo) is a new method for cancer immunotherapy. These nanoparticles with a size range of 30-120 nm are a small model of mother cells. In this study, the anti-tumor activity of NK-Exo and LAK-Exo (activated NK cell-derived exosome) against acute myeloid leukemia (AML) is investigated in vitro. Materials and Methods: The MACS method was performed for the separation of NK cells from the buffy coats of healthy donors, and an EXOCIBE kit was used for the isolation of NK-Exo.
After treating the KG-1 cell line with different doses of NK-Exo, MTT assay, and annexin V-PE were done to evaluate cell proliferation and apoptosis, respectively, and for confirmation of involved proteins, Real-Time PCR and western blotting were performed. Results: Anti-tumor activity of NK-Exo and LAK-Exo was dose- and time-dependent. Their highest activities were observed following 48 hours of incubation with 50 g/ml exosome (p<0. 0001).
However, this cytotoxic activity was also seen over a short period of time with low concentrations of NK-Exo (p<0. 05) and LAK-Exo (p<0. 001). The cytotoxic effect of LAK-Exo on target cells was significantly higher than NK-EXO. The induction of apoptosis by different pathways was time-point dependent. Total apoptosis was 34.
56% and 51. 6% after 48 hours of tumor cell coculture with 50 g/ml NK-Exo and LAK-Exo, respectively. Significant expression of CASPASE3 , P38, and CYTOCHROME C genes was observed in the cells treated with 50 g/ml NK-Exo and LAK-Exo. Conclusion : Our study confirmed the antileukemia activity of NK-Exo against AML tumor cells in vitro.
Therefore, NK-Exo can be considered as a promising and effective treatment for leukemia therapy.
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