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:Single-cell transcriptomics reveals comprehensive microenvironment and highlights the dysfuntional state of NK cells in endometrioid carcinoma.
Single-cell transcriptomics reveals comprehensive microenvironment and highlights the dysfuntional state of NK cells in endometrioid carcinoma.
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子宫内膜样子宫内膜癌(EEC)是最常见的妇科恶性肿瘤之一。癌细胞与肿瘤微环境(TME)细胞之间的相互作用,对疾病进展和治疗应答起关键作用。为更好地理解EEC微环境的多样性,我们对21份样本开展单细胞RNA测序的综合分析,其中包括16份EEC组织和5份邻近正常组织。研究重点关注肿瘤浸润自然杀伤(NK)细胞及其与其他免疫细胞类型之间的细胞间相互作用。我们发现一个CD56dim_DNAJB1 NK细胞亚群,其细胞毒能力低、应激水平高,提示该亚群处于功能失调状态。该亚群通过多组配体-受体对与肿瘤相关巨噬细胞强烈相互作用。此外,我们观察到肿瘤浸润LAMP3⁺树突状细胞可能抑制CD8⁺ T细胞,或招募调节性T细胞进入肿瘤区域。这些树突状细胞在TME中激活NK细胞的能力也受损。本研究加深了对NK细胞在肿瘤免疫中作用的认识,并突显靶向特定NK细胞亚群的潜在治疗价值。
Endometrioid endometrial cancer (EEC) is one of the most common gynecologic malignancies. The interaction between cancer cells and the cells in the tumor microenvironment (TME) plays a crucial role in determining disease progression and response to treatment. To better understand the diversity in the TME of ECC, we conducted a comprehensive analysis using single-cell RNA sequencing across 21 samples, including 16 ECC and 5 adjacent normal tissues.
We primarily focused on tumor-infiltrating natural killer (NK) cells and their cell-cell interactions with other immune cell types.
We identified a CD56dim_DNAJB1 NK cells subset, which had low cytotoxic capability and high stress levels, suggesting a dysfunctional state. This subset showed strong interactions with tumor-associated macrophages through several ligand-receptor pairs.
Additionally, we observed that tumor-infiltrating LAMP3+ dendritic cells may inhibit CD8+ T cells or attract regulatory T cells to the tumor area. These dendritic cells also had impaired activation effects on NK cells within the TME.
Our study provides valuable insights into the role of NK cells in cancer immunity and highlights the potential of targeting specific NK cell subsets for therapeutic purposes.
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