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:Nanobubble-based anti-hepatocellular carcinoma therapy combining immune check inhibitors and sonodynamic therapy.
Nanobubble-based anti-hepatocellular carcinoma therapy combining immune check inhibitors and sonodynamic therapy.
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肝细胞癌(HCC)是全球最常见的恶性肿瘤之一,对全球人类健康构成威胁,目前获批的治疗策略未能产生令人满意的结果。在此,我们制备了携带免疫检查点抑制剂(ICIs)、PD-L1抗体(PD-L1 Ab)和声动力剂二氢卟吩e6(Ce 6)的纳米气泡(NBs);从免疫和声动力治疗的角度分析了这些NBs的抗癌特性。PD-L1 Ab/Ce 6-NBs可通过调节活性氧(ROS)产生、细胞凋亡,以及最重要的是调节相关免疫细胞(包括NK 细胞和淋巴细胞)的功能来抑制肿瘤生长。在PD-L1 Ab/Ce 6-NB处理的小鼠中,肿瘤组织高表达免疫原性肿瘤细胞死亡(ICD)标志物,其中钙网蛋白(CRT)和ICD相关免疫细胞因子(CD80、CD86、INF-γ和IL-2)的表达增加。PD-L1 Ab/Ce 6-NBs还促进小鼠脾淋巴细胞增殖和细胞毒活性,以及肿瘤组织中CD8+ T细胞浸润,并下调PD-L1蛋白和mRNA表达。
此外,在小鼠皮下移植瘤模型中,Bax表达增加,Bcl-2在mRNA和蛋白水平受到抑制。这些结果表明,PD-L1 Ab/Ce 6-NBs可诱导ROS依赖性ICD,在靶向肿瘤微环境中PD-1/PD-L1免疫检查点的作用下进一步增强抗癌免疫应答,有望成为HCC的治疗药物。
Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, posing a global threat to human healthcare, and current approved treatment strategies do not produce satisfactory outcomes.
Here, nanobubbles (NBs) were prepared that carried Immune Check Inhibitors (ICIs), PD-L1 antibody (PD-L1 Ab) and sonodynamic agent CHLORIN E6 (Ce 6 ); the anti-cancer properties of these NBs were analyzed from the point of view of immune and sonodynamic therapies. The PD-L1 Ab/Ce 6 -NBs could inhibit tumor growth through regulating reactive oxygen species (ROS) production, apoptosis, and most importantly, the function of associated immunocytes, including natural killer cells and lymphocytes.
The tumor tissues highly expressed markers of immunogenic tumor cell death (ICD) in which the expression of calreticulin (CRT) and ICD-related immune cytokines (CD80, CD86, INF-γ, and IL-2) were increased in PD-L1 Ab/Ce 6 -NB treated mice. PD-L1 Ab/Ce 6 -NBs also promoted murine spleen lymphocyte proliferation and cytotoxic activity, as well as CD8+ T cell infiltration in the tumor tissues, and downregulation of the PD-L1 protein and mRNA expression.
Furthermore, Bax expression was increased and Bcl-2 was inhibited at the mRNA and protein levels in a murine subcutaneous transplanted tumor model. These results indicate that PD-L1 Ab/Ce 6 -NBs can induce ROS-dependent ICD to further boost anti-cancer immune responses under the action of targeting the PD-1/PD-L1 immune check point in the tumor microenvironment as a promising therapeutic agent for HCC.
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