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:CD95/Fas protects triple negative breast cancer from anti-tumor activity of NK cells.
CD95/Fas protects triple negative breast cancer from anti-tumor activity of NK cells.
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诱导细胞凋亡的受体CD95/Fas具有多种促肿瘤作用。既往在不同基因工程小鼠模型中,肿瘤表达CD95被证明对细胞生长至关重要。本研究结合免疫缺陷和免疫功能健全小鼠模型,发现转移性三阴性乳腺癌(TNBC)细胞丢失CD95后,可通过调节免疫图谱阻止肿瘤生长。CD95缺失肿瘤在免疫功能健全环境中几乎不生长,且肿瘤内免疫细胞浸润增加;这种生长抑制由浸润NK细胞介导,不涉及T细胞或巨噬细胞。相反,在免疫缺陷小鼠中,CD95敲除细胞的生长未受抑制,但无法形成转移灶。综上,除了促进肿瘤和转移外,肿瘤细胞表达CD95还可对NK细胞发挥免疫抑制作用,为免疫治疗提供了新靶点。
The apoptosis inducing receptor CD95/Fas has multiple tumorigenic activities. In different genetically engineered mouse models tumor-expressed CD95 was shown to be critical for cell growth. Using a combination of immune-deficient and immune-competent mouse models, we now establish that loss of CD95 in metastatic triple negative breast cancer (TNBC) cells prevents tumor growth by modulating the immune landscape. CD95-deficient, but not wild-type, tumors barely grow in an immune-competent environment and show an increase in immune infiltrates into the tumor.
This growth reduction is caused by infiltrating NK cells and does not involve T cells or macrophages. In contrast, in immune compromised mice CD95 k. o. cells are not growth inhibited, but they fail to form metastases. In summary, we demonstrate that in addition to its tumor and metastasis promoting activities, CD95 expression by tumor cells can exert immune suppressive activities on NK cells, providing a new target for immune therapy.
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