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首页> 外文期刊>Cancer Cell International >PA-MSHA induces apoptosis and suppresses metastasis by tumor associated macrophages in bladder cancer cells
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PA-MSHA induces apoptosis and suppresses metastasis by tumor associated macrophages in bladder cancer cells

机译:PA-MSHA诱导膀胱癌细胞中肿瘤相关巨噬细胞凋亡并抑制其转移

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Background The aim of the present study was to investigate effects of Pseudomonas aeruginosa -mannose-sensitive hemagglutinin (PA-MSHA) on the inhibition of the proliferation of bladder cancer cell lines and to further define its functional mechanisms. Methods A rat model of bladder tumor was induced by intravesical N-methyl-N nitrosourea. The dynamic growth of tumor was measured by whole-body fluorescent imaging system. Morphological analysis was observed by hematoxylin–eosin staining and microscopic examination. The expression of Caspase 3 and E-Ca were detected by immunohistochemistry technique. Macrophages were separated by flow cytometry. The expression of cytokines was measured by qRT-PCR and western blot. Apoptosis ability was conducted by means of annexin V and propidium iodide. The abilities of invasion and migration were determined by transwell migration assay and scratch assay. Results PA-MSHA and PA-MSHA?+?Fisetin groups inhibited the growth of tumor and increased the ratio of M1/M2. For one thing, PA-MSHA suppressed the invasive ability of the bladder tumor cell and promoted bladder tumor cell apoptosis. For another, it facilitated the expression of M1 cytokines and reduced expression of M2 cytokines. Furthermore, treated with PA-MSHA, mouse M1 phagocytosis rates were higher than that of M2 macrophages for bladder cancer lines. Conclusions The data revealed that PA-MSHA might promote apoptosis and inhibit proliferation, invasion and migration of mouse bladder cancer cells by inducing M1 polarization.
机译:背景技术本研究的目的是研究铜绿假单胞菌-甘露糖敏感性血凝素(PA-MSHA)对膀胱癌细胞系增殖的抑制作用,并进一步确定其功能机制。方法采用膀胱内N-甲基-N亚硝基脲诱导膀胱癌模型。通过全身荧光成像系统测量肿瘤的动态生长。通过苏木精-伊红染色和显微镜检查观察形态。免疫组织化学法检测Caspase 3和E-Ca的表达。通过流式细胞术分离巨噬细胞。通过qRT-PCR和western blot检测细胞因子的表达。通过膜联蛋白V和碘化丙啶进行凋亡能力。通过transwell迁移测定法和刮擦测定法测定侵袭和迁移能力。结果PA-MSHA和PA-MSHAβ+?Fisetin组抑制了肿瘤的生长并增加了M1 / M2的比例。一方面,PA-MSHA抑制了膀胱肿瘤细胞的侵袭能力并促进了膀胱肿瘤细胞的凋亡。另一方面,它促进了M1细胞因子的表达并降低了M2细胞因子的表达。此外,用PA-MSHA处理后,对于膀胱癌细胞系,小鼠M1吞噬率高于M2巨噬细胞。结论数据显示PA-MSHA可能通过诱导M1极化来促进小鼠膀胱癌细胞的凋亡并抑制其增殖,侵袭和迁移。

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