γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
我们的发现表明,活化的γδ T细胞可能是SCLC治疗的有价值靶点。
英文原题:MVs and MVs-Crocin as Novel Therapeutic Agents for Lung Cancer, Apoptosis, and Gene Regulation.
MVs and MVs-Crocin as Novel Therapeutic Agents for Lung Cancer, Apoptosis, and Gene Regulation.
MVs和MVs-Crocin均通过降低肺癌细胞存活率和诱导凋亡表现出强效抗癌作用。用Crocin预处理似乎进一步增强了MVs的治疗效果。重要的是,与正常细胞相比,这些作用在癌细胞中更为明显,表明具有选择性抗癌潜力。MVs和MVs-Crocin促进肺癌细胞凋亡,可能成为开发肺癌新型治疗策略的有前景候选方案。
肺癌是全球最常见的恶性肿瘤之一。干细胞及其分泌物因其抗癌特性近年来作为潜在治疗剂受到关注。本研究探讨了间充质干细胞来源的微囊泡(MVs)和藏红花素预处理微囊泡(MVs-Crocin)对肺癌细胞(A549)的影响,并与正常细胞(HEK293)进行比较。
间充质干细胞经藏红花素预处理后,分离微囊泡。采用MTT法确定MVs和MVs-Crocin的适宜治疗浓度。以优化剂量处理A549和HEK293细胞。通过流式细胞术评估凋亡,并通过实时PCR分析凋亡基因的表达。
MTT实验确定MVs的最佳治疗浓度为40 g/ml,MVs-Crocin为50 g/ml。MVs和MVs-Crocin治疗显著降低了A549细胞的存活率,同时凋亡实验和基因表达分析证实了处理后的癌细胞凋亡活性增强。
INTRODUCTION: Lung cancer is one of the most common malignancies worldwide. Stem cells and their secretions have recently attracted attention as potential therapeutic agents due to their anti-cancer properties. This study investigated the effects of mesenchymal stem cell-derived microvesicles (MVs) and Crocinpreconditioned MVs (MVs-Crocin) on lung cancer cells (A549) compared with normal cells (HEK293). MATERIALS AND METHODS: Mesenchymal stem cells were preconditioned with Crocin, and microvesicles were subsequently isolated. The appropriate therapeutic concentrations of MVs and MVs-Crocin were determined using the MTT assay. A549 and HEK293 cells were treated with the optimized doses. Apoptosis was assessed by flow cytometry, and the expression of apoptotic genes was analyzed through real-time PCR. RESULTS: MTT assay results identified 40 g/ml for MVs and 50 g/ml for MVs-Crocin as optimal therapeutic concentrations. Treatment with MVs and MVs-Crocin significantly reduced the survival of A549 cells, while apoptosis assays and gene expression analysis confirmed enhanced apoptotic activity in treated cancer cells. DISCUSSION: Both MVs and MVs-Crocin demonstrated potent anti-cancer effects by reducing lung cancer cell survival and inducing apoptosis. Preconditioning with Crocin appeared to further strengthen the therapeutic efficacy of MVs. Importantly, these effects were more pronounced in cancer cells compared to normal cells, indicating selective anti-cancer potential. CONCLUSION: MVs and MVs-Crocin promote apoptosis in lung cancer cells and may serve as promising candidates for the development of novel therapeutic strategies against lung cancer.
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