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:Synergistic effect of human uterine cervical mesenchymal stem cell secretome and paclitaxel on triple negative breast cancer.
Synergistic effect of human uterine cervical mesenchymal stem cell secretome and paclitaxel on triple negative breast cancer.
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我们的数据表明,CM-hUCESC 与紫杉醇联合在 TNBC 中具有协同作用,并提供了降低化疗药物剂量的机会,从而可能减轻化疗相关毒性。
三阴性乳腺癌(TNBC)是乳腺癌中致死性最高的亚型。尽管化疗有不良反应,仍是 TNBC 的标准全身治疗。由于联合不同药物以提高疗效和治愈潜力至关重要,间充质干细胞(MSC)分泌组可能是一种创新替代方案。
本研究拟探讨化疗药物紫杉醇与复杂生物制品——人宫颈干细胞分泌组(CM-hUCESC)联合用于 TNBC 的抗肿瘤作用。
紫杉醇与 CM-hUCESC 联合可降低肿瘤细胞增殖和侵袭性,并在体外诱导细胞凋亡(MDA-MB-231 细胞和/或原代肿瘤细胞)。小鼠肿瘤异种移植模型证实了抗肿瘤作用,两种制品联合可显著抑制肿瘤生长。此外,以亚致死剂量紫杉醇对 hUCESC 预处理,可增强其分泌组作用;与紫杉醇联合后进一步显著抑制肿瘤生长,甚至可降低体内紫杉醇剂量。这种效应部分由 CM-hUCESC 来源的细胞外囊泡(EV)及 TIMP-1 和 TIMP-2 等可溶性因子介导。
数据表明 CM-hUCESC 与紫杉醇联合对 TNBC 具有协同作用,并为降低化疗药物剂量提供可能,从而或可减少化疗相关毒性。
Triple-negative breast cancer (TNBC) is the most lethal subtype of breast cancer and, despite its adverse effects, chemotherapy is the standard systemic treatment option for TNBC. Since, it is of utmost importance to consider the combination of different agents to achieve greater efficacy and curability potential, MSC secretome is a possible innovative alternative.
In the present study, we proposed to investigate the anti-tumor effect of the combination of a chemical agent (paclitaxel) with a complex biological product, secretome derived from human Uterine Cervical Stem cells (CM-hUCESC) in TNBC.
The combination of paclitaxel and CM-hUCESC decreased cell proliferation and invasiveness of tumor cells and induced apoptosis in vitro (MDA-MB-231 and/or primary tumor cells). The anti-tumor effect was confirmed in a mouse tumor xenograft model showing that the combination of both products has a significant effect in reducing tumor growth. Also, pre-conditioning hUCESC with a sub-lethal dose of paclitaxel enhances the effect of its secretome and in combination with paclitaxel reduced significantly tumor growth and even allows to diminish the dose of paclitaxel in vivo. This effect is in part due to the action of extracellular vesicles (EVs) derived from CM-hUCESC and soluble factors, such as TIMP-1 and - 2.
In conclusion, our data demonstrate the synergistic effect of the combination of CM-hUCESC with paclitaxel on TNBC and opens an opportunity to reduce the dose of the chemotherapeutic agents, which may decrease chemotherapy-related toxicity.
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