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:Treatment of Mesenchymal Stem Cell-Derived Extracellular Vesicles with Extract of Cultured Lentinula edodes Modulates Breast Cancer Stem Cells and MicroRNA Reprogramming.
Treatment of Mesenchymal Stem Cell-Derived Extracellular Vesicles with Extract of Cultured Lentinula edodes Modulates Breast Cancer Stem Cells and MicroRNA Reprogramming.
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乳腺癌是加拿大女性中最常见的恶性肿瘤,固有性或获得性耐药显著增加复发和转移的风险。尽管一线治疗是多模式的,但化疗耐药仍然是治疗中的主要障碍,而目前认为摄入发酵过程产生的天然化合物是克服这一问题的有效策略。本研究探讨了经培养的香菇提取物(AHCC)预处理的间充质基质/干细胞(MSCs)来源的细胞外囊泡(EVs)对降低化疗耐药性和调节MCF-7及MCF-7/DOX细胞系中microRNAs的影响。使用纳米颗粒追踪分析对EV进行表征,并研究了microRNAs和癌症干细胞的形成。miRNA分析显示,AHCC显著下调致癌性miR-155,但上调抑瘤性microRNAs miR-34a、miR-Let7a和miR-200c。体外实验显示,用AHCC预处理的EVs处理细胞后,癌症干细胞增殖受到抑制。结论:我们的数据表明,AHCC可能有助于调节肿瘤微环境,从而影响癌症干细胞的发展。
Breast carcinoma represents the most frequent malignancy in women in Canada, and intrinsic or acquired drug resistance significantly increases the risk of recurrence and metastasis. Although front-line therapy is multimodal, chemoresistance remains a major hurdle in treatment and therapy, and the intake of natural compounds resulting from fermentation processes is currently considered an effective strategy to overcome this problem.
This study investigated the effect of extracellular vesicles (EVs) from Mesenchymal Stromal/stem cells (MSCs) pretreated with cultured Lentinula edodes extract (AHCC) on reducing chemoresistance and modulating microRNAs in the MCF-7 and MCF-7/DOX cell lines. EV characterization was performed using nanoparticle tracking analysis, and microRNAs and the formation of cancer stem cells were studied.
The miRNA analysis revealed that AHCC significantly downregulated oncogenic miR-155 but upregulated the tumor-suppressive microRNAs miR-34a , miR-Let7a , and miR-200c . In vitro experiments showed inhibition of cancer stem cell proliferation after challenging the cells with AHCC-pretreated EVs. Conclusion: Our data demonstrated that AHCC may contribute to modulation of the tumor microenvironment, thus influencing the development of cancer stem cells.
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