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:The nuclear export protein XPO1 provides a peptide ligand for natural killer cells.
The nuclear export protein XPO1 provides a peptide ligand for natural killer cells.
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XPO1(Exportin-1/CRM1)是一种核输出蛋白,在癌症中常过表达,并作为肿瘤发生的驱动因素发挥作用。目前,靶向XPO1的小分子正作为抗癌药物在临床中使用。我们将XPO1确定为自然杀伤(NK)细胞的靶点。利用免疫肽组学,我们鉴定出一种来源于XPO1的肽,其可在人类白细胞抗原-C的背景下被活化性NK细胞受体KIR2DS2识别。该肽可被内源性加工并呈递,以通过该受体特异性激活NK细胞。尽管癌症中XPO1高表达通常与不良预后相关,但我们表明,如果同时存在NK细胞浸润的证据,某些特定癌症(如肝细胞癌)的结局可显著改善。因此,我们将XPO1确定为一种被NK细胞识别的真正的肿瘤抗原,其为实体瘤NK细胞治疗的个体化方法提供了机会。
XPO1 (Exportin-1/CRM1) is a nuclear export protein that is frequently overexpressed in cancer and functions as a driver of oncogenesis. Currently small molecules that target XPO1 are being used in the clinic as anticancer agents.
We identify XPO1 as a target for natural killer (NK) cells. Using immunopeptidomics, we have identified a peptide derived from XPO1 that can be recognized by the activating NK cell receptor KIR2DS2 in the context of human leukocyte antigen-C. The peptide can be endogenously processed and presented to activate NK cells specifically through this receptor.
Although high XPO1 expression in cancer is commonly associated with a poor prognosis, we show that the outcome of specific cancers, such as hepatocellular carcinoma, can be substantially improved if there is concomitant evidence of NK cell infiltration.
We thus identify XPO1 as a bona fide tumor antigen recognized by NK cells that offers an opportunity for a personalized approach to NK cell therapy for solid tumors.
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