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:Enhanced antitumor efficacy of mesenchymal stem cells expressing cytosine deaminase and 5-fluorocytosine combined with α-galactosylceramide in a colon cancer model.
Enhanced antitumor efficacy of mesenchymal stem cells expressing cytosine deaminase and 5-fluorocytosine combined with α-galactosylceramide in a colon cancer model.
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癌症免疫治疗已成为治疗多种恶性肿瘤的一种有前景的方法。在本研究中,我们探讨了表达胞嘧啶脱氨酶的间充质干细胞(MSC/CD)和5-氟胞嘧啶(5-FC)与α-半乳糖神经酰胺(α-GalCer)联合在结肠癌模型中的治疗效果。我们的研究结果表明,与单独治疗相比,MSC/CD、5-FC和α-GalCer的联合治疗产生了增强的抗肿瘤活性。这表现为肿瘤微环境中免疫细胞浸润增加,如自然杀伤T(NKT)细胞、抗原呈递细胞(APCs)、T细胞和自然杀伤(NK)细胞,以及促炎细胞因子和趋化因子表达升高。此外,我们观察到联合治疗后没有明显的肝毒性。我们的研究强调了MSC/CD、5-FC和α-GalCer联合用于结肠癌治疗的潜在治疗益处,并为癌症免疫治疗领域提供了有价值的见解。未来的研究应侧重于阐明其潜在机制,并探索这些发现对其他癌症类型和免疫治疗策略的适用性。
Cancer immunotherapy has emerged as a promising approach for treating various malignancies. In this study, we investigated the combined therapeutic effects of mesenchymal stem cells expressing cytosine deaminase (MSC/CD) and 5-fluorocytosine (5-FC) with α-galactosylceramide (α-GalCer) in a colon cancer model.
Our findings demonstrated that the combination of MSC/CD, 5-FC, and α-GalCer resulted in enhanced antitumor activity compared to the individual treatments. This was evidenced by increased infiltration of immune cells, such as natural killer T (NKT) cells, antigen-presenting cells (APCs), T cells, and natural killer (NK) cells, in the tumor microenvironment, as well as elevated expression of proinflammatory cytokines and chemokines.
Furthermore, we observed no significant hepatotoxicity following the combined treatment.
Our study highlights the potential therapeutic benefits of combining MSC/CD, 5-FC, and α-GalCer for colon cancer treatment and contributes valuable insights to the field of cancer immunotherapy. Future research should focus on elucidating the underlying mechanisms and exploring the applicability of these findings to other cancer types and immunotherapy strategies.
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