CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
我们的工作确立了CD81作为连接放射抵抗与免疫逃逸的关键桥梁,其通过维持GBM中CD274的丰度发挥作用,并突显CD81作为优化放射免疫治疗的有前景的治疗靶点。
英文原题:Exploring the Therapeutic Potential of Extracellular Vesicles Derived from Human Immature Dental Pulp Cells on Papillary Thyroid Cancer.
间充质干细胞来源的细胞外囊泡(MSC-EVs)在癌症治疗和药物递送方面已得到越来越多的研究,它们提供了一种先进的无细胞治疗选择。
间充质干细胞来源的细胞外囊泡(MSC-EVs)在癌症治疗和药物递送方面的研究日益增多,它们提供了一种先进的无细胞治疗选择。然而,其总体效应和疗效取决于多种因素,包括MSC来源和货物内容物。在本研究中,我们从人未成熟牙髓干细胞的条件培养基中分离了EVs(hIDPSC-EVs),并研究了它们对两种甲状腺乳头状癌(PTC)细胞系(BCPAP和TPC1)的影响。我们观察到两种PTC细胞系均能有效摄取hIDPSC-EVs,并对基因调控产生显著影响,尤其是在BCPAP细胞的Wnt信号通路中。然而,未观察到对细胞增殖的显著影响。相反,hIDPSC-EVs在治疗120 h后显著降低了两种PTC细胞系的侵袭能力。这些体外研究结果提示hIDPSC-EVs在癌症管理中的治疗潜力,并强调需要进一步研究以开发新型有效的治疗策略。此外,PTC细胞系对hIDPSC-EVs的成功内化凸显了其作为抗癌药物纳米载体的潜在用途。
Mesenchymal stem-cell-derived extracellular vesicles (MSC-EVs) have been increasingly investigated for cancer therapy and drug delivery, and they offer an advanced cell-free therapeutic option. However, their overall effects and efficacy depend on various factors, including the MSC source and cargo content. In this study, we isolated EVs from the conditioned medium of human immature dental pulp stem cells (hIDPSC-EVs) and investigated their effects on two papillary thyroid cancer (PTC) cell lines (BCPAP and TPC1). We observed efficient uptake of hIDPSC-EVs by both PTC cell lines, with a notable impact on gene regulation, particularly in the Wnt signaling pathway in BCPAP cells. However, no significant effects on cell proliferation were observed. Conversely, hIDPSC-EVs significantly reduced the invasive capacity of both PTC cell lines after 120 h of treatment. These in vitro findings suggest the therapeutic potential of hIDPSC-EVs in cancer management and emphasize the need for further research to develop novel and effective treatment strategies. Furthermore, the successful internalization of hIDPSC-EVs by PTC cell lines underscores their potential use as nanocarriers for anti-cancer agents.
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