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:NK cells and solid tumors: therapeutic potential and persisting obstacles.
NK cells and solid tumors: therapeutic potential and persisting obstacles.
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自然杀伤(NK)细胞是一种具有强大细胞毒活性的固有淋巴细胞,近年来作为潜在抗癌治疗手段受到关注。虽然NK细胞在白血病患者中介导令人鼓舞的反应,但NK细胞输注在实体瘤患者中的治疗效果有限。临床前和临床数据表明,NK细胞输注对实体恶性肿瘤的疗效受到多种因素阻碍,包括肿瘤浸润不足以及在肿瘤微环境(TME)中的持续存在/激活不足。TME的多种代谢特征,包括缺氧以及腺苷、活性氧和前列腺素水平升高,对NK细胞活性产生负面影响。此外,癌症相关成纤维细胞、肿瘤相关巨噬细胞、髓源性抑制细胞和调节性T细胞主动抑制NK细胞依赖性抗癌免疫。在此,我们综述了抑制实体肿瘤中NK细胞的代谢和细胞屏障,并讨论了克服这些障碍以实现更优治疗活性的潜在策略。
Natural killer (NK) cells, which are innate lymphocytes endowed with potent cytotoxic activity, have recently attracted attention as potential anticancer therapeutics. While NK cells mediate encouraging responses in patients with leukemia, the therapeutic effects of NK cell infusion in patients with solid tumors are limited.
Preclinical and clinical data suggest that the efficacy of NK cell infusion against solid malignancies is hampered by several factors including inadequate tumor infiltration and persistence/activation in the tumor microenvironment (TME). A number of metabolic features of the TME including hypoxia as well as elevated levels of adenosine, reactive oxygen species, and prostaglandins negatively affect NK cell activity.
Moreover, cancer-associated fibroblasts, tumor-associated macrophages, myeloid-derived suppressor cells, and regulatory T cells actively suppress NK cell-dependent anticancer immunity.
Here, we review the metabolic and cellular barriers that inhibit NK cells in solid neoplasms as we discuss potential strategies to circumvent such obstacles towards superior therapeutic activity.
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