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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Enhanced anti-tumor efficacy of S3I-201 in breast cancer mouse model through Wharton jelly- exosome.
Enhanced anti-tumor efficacy of S3I-201 in breast cancer mouse model through Wharton jelly- exosome.
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我们的结果表明,WJ-Exo 是一种有效的载体,能够将 S3I-201 靶向递送至肿瘤细胞,并增强 S3I-201 在荷瘤小鼠中的治疗效果。
外泌体是存在于多种细胞类型(包括沃顿胶间充质干细胞)中的膜包被囊泡,在细胞间通讯和调控中发挥关键作用。其作为无细胞纳米技术和药物递送系统的应用已引起关注。三阴性乳腺癌(TNBC)是重大的全球健康问题,以高死亡率为特征。本研究探讨沃顿胶间充质干细胞来源外泌体(WJ-Exo)作为S3I-201载体的潜力及其对乳腺癌细胞系中STAT3表达的影响,并评估这些外泌体是否能增强S3I-201的抗肿瘤效果。
过滤后的WJ-Exos通过透射电子显微镜(TEM)、扫描电子显微镜(SEM)、动态光散射(DLS)、流式细胞术和Western blotting进行分析。随后将这些外泌体用于负载S3I-201,形成纳米制剂WJ-Exo(S3I-201)。在体外使用MTT assay、流式细胞术、伤口愈合实验、Western blotting和定量实时聚合酶链反应(qPCR)分析研究了WJ-Exo(S3I-201)对4T1癌细胞的影响。最后,在体内使用荷瘤小鼠模型研究了该纳米制剂的治疗效果。
体外实验表明,将4T1细胞与纳米制剂共孵育后,p-STAT3水平显著降低,诱导凋亡,调节Bcl-2、Bax和caspase-3蛋白及基因表达,并抑制迁移。在体内,用WJ-Exo(S3I-201)治疗荷瘤小鼠显示出强大的抗肿瘤效果,超过了在S3I-201组中观察到的疗效。
Exosomes, membrane-enveloped vesicles found in various cell types, including Wharton's jelly mesenchymal stem cells, play a crucial role in intercellular communication and regulation. Their use as a cell-free nanotechnology and drug delivery system has attracted attention. Triple-negative breast cancer (TNBC) is a major global health problem and is characterized by a high mortality rate. This study investigates the potential of Wharton's Jelly mesenchymal stem cell-derived exosomes (WJ-Exo) as carriers of S3I-201 and their effects on STAT3 expression in breast cancer cell lines, and evaluates whether these exosomes can enhance the anti-tumor effect of S3I-201.
The filtered WJ-Exos were analyzed by Transmission Electron Microscopy (TEM), Scanning electron microscopy (SEM), Dynamic Light Scattering (DLS), flow cytometry, and Western blotting. These exosomes were then used for loading with S3I-201, resulting in the nano-formulation WJ-Exo(S3I-201). The effect of WJ-Exo(S3I-201) on 4T1 cancer cells was investigated in vitro using MTT assay, flow cytometry, wound healing assay, Western blotting and Quantitative Real-Time Polymerase chain reaction (qPCR) analysis. Finally, the therapeutic efficacy of the nano-formulation was investigated in vivo using a tumor-bearing mouse model.
In vitro experiments showed that co-incubation of 4T1 cells with the nano-formulation resulted in a significant reduction in p-STAT3 levels, induction of apoptosis, modulation of Bcl-2, Bax and caspase-3 protein and gene expression, and inhibition of migration. In vivo, treatment of tumor-bearing mice with WJ-Exo(S3I-201) showed a strong antitumor effect that exceeded the efficacy observed in the S3I-201 group.
Our results demonstrate that WJ-Exo is an effective carrier for targeting S3I-201 to tumor cells and enhances the therapeutic efficacy of S3I-201 in tumor-bearing mice.
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