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:Black phosphorus-Au-thiosugar nanosheets mediated photothermal induced anti-tumor effect enhancement by promoting infiltration of NK cells in hepatocellular carcinoma.
Black phosphorus-Au-thiosugar nanosheets mediated photothermal induced anti-tumor effect enhancement by promoting infiltration of NK cells in hepatocellular carcinoma.
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新型 BATNS 可提高 BPNS 的稳定性,同时将癌症热疗与由局部 NK 细胞浸润引导的免疫治疗相结合,从而对肝细胞癌产生更好的治疗效果。这项工作也为设计基于 BP 的生物医学应用材料提供了新途径。
肝细胞癌(HCC)是一种异质性癌症,需要联合治疗,如光热治疗和化疗。近年来,癌症免疫疗法迅速发展,是治疗恶性肿瘤最有前景的途径之一。因此,将传统疗法与免疫疗法结合在一个平台上,可能会提高HCC治疗的疗效。
在这项工作中,我们制备了一种黑磷(BP)-Au-硫糖纳米片(BATNS),其中Au-硫糖涂层和功能化提高了黑磷纳米片(BPNS)和金离子在不同模拟生理环境中的稳定性。与BPNS相比,BATNS带隙的压缩可以将更多的光子能量转化为热量,从而获得更高的光热转换效率。体外和体内结果还显示,与BPNS相比,BATNS对小鼠肝细胞癌的抑制作用更强,并延长了疾病模型的生存期。更重要的是,BATNS在肝癌治疗中表现出额外的免疫效应,即增加局部NK细胞浸润而不增加T细胞,而这种免疫效应是由BATNS光热治疗的热效应引起的。
Hepatocellular carcinoma (HCC) is a heterogeneous cancer required combination therapy, such as photothermal therapy and chemotherapy. In recent years, cancer immunotherapies are rapidly evolving and are some of the most promising avenues to approach malignancies. Thus, the combination of the traditional therapies and immunotherapy in one platform may improve the efficacy for HCC treatment.
In this work, we have prepared a black phosphorus (BP)-Au-thiosugar nanosheets (BATNS), in which Au-thiosugar coating and functionalization improved the stability of both black phosphorus nanosheets (BPNS) and gold ions in different simulated physiological environments. The compression of the BATNS band gap can convert more photon energy to heat generation compared with BPNS, resulting in higher photothermal conversion efficiency. The in vitro and in vivo results also revealed a stronger reduction on the hepatocellular carcinoma of mice and prolonged survival of disease models compared with BPNS. More importantly, BATNS showed an additional immune effect by increasing local NK cell infiltration but not T cell on the liver cancer treatment, and this immune effect was caused by the thermal effect of BATNS photothermal treatment.
The novel BATNS could improve the stability of BPNS and simultaneously combine the cancer thermotherapy and immunotherapy leaded by local NK cell infiltration, resulting in a better therapeutic efficacy on hepatocellular carcinoma. This work also provided a new path to design BP-based materials for biomedical applications.
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