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:Mesenchymal Stem/Stromal cells in solid tumor Microenvironment: Orchestrating NK cell remodeling and therapeutic insights.
Mesenchymal Stem/Stromal cells in solid tumor Microenvironment: Orchestrating NK cell remodeling and therapeutic insights.
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间充质干/基质细胞(MSCs)来源于正常组织,具有归巢至肿瘤部位并分化为肿瘤相关MSCs(TA-MSCs)的能力,后者在塑造肿瘤内免疫抑制微环境中发挥重要作用。自然杀伤(NK)细胞是固有免疫系统的重要组成部分,具有自主清除靶细胞的能力,可作为对抗肿瘤生长的即时防御力量。然而,在肿瘤微环境(TME)中,NK细胞的数量和功能常出现下降。TA-MSCs已被证实对肿瘤浸润免疫细胞尤其是NK细胞的功能产生深度抑制作用。理解TA-MSCs导致NK细胞功能障碍的机制,对于推进免疫监视和增强杀瘤反应至关重要。本综述总结了关于TME中TA-MSCs对NK细胞调控的现有文献,并提出增强抗肿瘤免疫的创新策略。
Mesenchymal stem/stromal cells (MSCs), originating from normal tissues, possess the capacity to home to tumor sites and differentiate into tumor-associated MSCs (TA-MSCs), which are instrumental in shaping an immunosuppressive milieu within tumors. Natural killer (NK) cells, integral to the innate immune system, are endowed with the ability to eradicate target cells autonomously, serving as an immediate defense against neoplastic growths. Nonetheless, within the tumor microenvironment (TME), NK cells often exhibit a decline in both their numerical presence and functionality.
TA-MSCs have been shown to exert profound inhibitory effects on the functions of tumor-infiltrating immune cells, notably NK cells. Understanding the mechanisms by which TA-MSCs contribute to NK cell dysfunction is critical for the advancement of immune surveillance and the enhancement of tumoricidal responses. This review summarizes existing literature on NK cell modulation by TA-MSCs within the TME and proposes innovative strategies to augment antitumor immunity.
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