借力推动前列腺癌 CAR-T 细胞治疗进展
Piggybacking toward Progress for CAR T-Cell Therapy in Prostate Cancer.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Ultrasound-mediated microbubbles cavitation enhanced chemotherapy of advanced prostate cancer by increasing the permeability of blood-prostate barrier.
Ultrasound-mediated microbubbles cavitation enhanced chemotherapy of advanced prostate cancer by increasing the permeability of blood-prostate barrier.
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尽管化疗是晚期前列腺癌的重要治疗手段,但其疗效相对有限。超声诱导的空化在药物递送和基因转染中发挥重要作用。然而,空化能否提高前列腺癌化疗的疗效仍不清楚。在本研究中,我们用超声介导的微泡空化联合紫杉醇处理RM-1小鼠前列腺癌细胞。我们的结果显示,联合治疗导致更明显的细胞活力抑制和细胞凋亡增加。化疗疗效的增强归因于空化诱导的细胞通透性增加。重要的是,与单纯化疗(nab-paclitaxel)相比,化疗联合超声介导的微泡空化在RM-1前列腺癌原位小鼠模型中显著抑制肿瘤生长并延长荷瘤小鼠的生存期,表明联合治疗对肿瘤缩小的协同效应。此外,我们分析了TIL(肿瘤浸润淋巴细胞),发现在化疗期间,空化处理后CD8 + T细胞中CTLA4 + 细胞和PD-1 + /CTLA4 + 细胞的比例略有增加。
Although chemotherapy is an important treatment for advanced prostate cancer, its efficacy is relatively limited. Ultrasound-induced cavitation plays an important role in drug delivery and gene transfection.
However, whether cavitation can improve the efficacy of chemotherapy for prostate cancer remains unclear. In this study, we treated RM-1 mouse prostate carcinoma cells with a combination of ultrasound-mediated microbubble cavitation and paclitaxel.
Our results showed that combination therapy led to a more pronounced inhibition of cell viability and increased cell apoptosis. The enhanced efficacy of chemotherapy was attributed to the increased cell permeability induced by cavitation.
Importantly, compared with chemotherapy alone (nab-paclitaxel), chemotherapy combined with ultrasound-mediated microbubble cavitation significantly inhibited tumor growth and prolonged the survival of tumor-bearing mice in an orthotopic mouse model of RM-1 prostate carcinoma, indicating the synergistic effects of combined therapy on tumor reduction.
Furthermore, we analyzed tumor-infiltrating lymphocytes and found that during chemotherapy, the proportions of CTLA4 + cells and PD-1 + /CTLA4 + cells in CD8 + T cells slightly increased after cavitation treatment.
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