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:Immune cell lncRNAs reprogram the tumor microenvironment.
Immune cell lncRNAs reprogram the tumor microenvironment.
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长链非编码 RNA(lncRNA)调控肿瘤微环境(TME),但其在 TME 免疫细胞群中的细胞内在作用仍被低估。在本综述中,我们将焦点从癌细胞转向免疫区室,系统回顾免疫细胞内在 lncRNA 如何调控 CD8 + T 细胞耗竭、CD4 + T 细胞极化、NK 细胞细胞毒性、树突状细胞抗原呈递以及巨噬细胞炎症编程。我们重点介绍作为分子开关发挥作用的 lncRNA——使免疫细胞在抗肿瘤效应状态与免疫抑制状态之间倾斜——并探讨外泌体 lncRNA 如何将这些调控回路延伸至 TME 内跨细胞边界。最后,我们评估基于 lncRNA 的生物标志物和旨在靶向免疫格局的治疗机会,并概述将免疫内在 lncRNA 生物学整合到精准免疫肿瘤学中的框架。
Long noncoding RNAs (lncRNAs) regulate the tumor microenvironment (TME), yet their cell-intrinsic roles within immune populations of the TME remain underappreciated. In this review, we shift focus from the cancer cell to the immune compartment, systematically reviewing how immune cell-intrinsic lncRNAs govern CD8 + T cell exhaustion, CD4 + T cell polarization, NK cell cytotoxicity, dendritic cell antigen presentation, and macrophage inflammatory programming.
We highlight lncRNAs that function as molecular switches-tipping immune cells between antitumor effector and immunosuppressive states-and examine how exosomal lncRNAs extend these regulatory circuits across cellular boundaries within the TME.
Finally, we evaluate opportunities for lncRNA-based biomarkers and therapies designed to target the immune landscape, outlining a framework for integrating immune-intrinsic lncRNA biology into precision immuno-oncology.
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