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PDT and Aspirin cause proteasome malfunctioning in human-derived lung adenocarcinoma cells

机译:PDT和阿司匹林导致人源性肺腺癌细胞中的蛋白酶态发生

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In this paper we reported that PDT and Aspirin individually induce a fast "but not irreversible" stall of proteasome activity of human lung carcinoma cell A549 (p53+/+) and H1299 (p53-/-). We demonstrated that this arrest can be protracted by their combination. More important, this combination stimulates apoptosis in these cancer cells prospecting enhanced therapeutic efficacy.Photodynamic therapy (PDT) of cancer involves administration of a tumor-localizing photosensitizer agent that, upon light stimulation, mediates cell destruction via production of singlet oxygen.Although side-effects void, PDT has a narrow field of application being currently used to treat selected cancer forms.
机译:在本文中,我们报道了PDT和阿司匹林单独诱导人肺癌细胞A549(P53 + / +)和H1299(P53 - / - )的蛋白酶体活性的快速“但不可逆转的”术。我们证明,这种逮捕可以通过它们的组合来延伸。更重要的是,这种组合刺激了这些癌细胞中的细胞凋亡,前景提高了治疗效果。癌症的电动力治疗(PDT)涉及施用肿瘤定位的光敏剂剂,在光刺激后,通过生产偏出侧面介导细胞破坏。虽然侧面 - 效果空隙,PDT目前用于治疗选定的癌症形式的狭窄申请领域。

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