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Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer

机译:小鼠原位膀胱癌进展过程中的肿瘤和微环境改变

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The aim of this study was to monitor changes in the expression of immune-related genes in the bladder after tumor implantation. Mice were orthotopically implanted with MB49-PSA cells (C57BL/6 mice) on day 1 and terminated on days 7, 14, 21, and 28. Another mouse model (MBT-2/C3H mice) was examined at day 7. Gene expression analysis was performed using a TaqMan Low Density Mouse Immune Panel (Applied Biosystems, USA) on RNA extracted from the bladders. Selected genes were reconfirmed by real-time PCR analysis and RT-PCR on the mRNA from other animals. Immune suppressive (IL13, IL1 β , PTGS2, NOS2, IL10, CTLA4, and CCL22) and immune stimulatory genes (CSF2, GZMB, IFN γ , CXCL10, TNF α , CD80, IL12a, and IL6) and AGTR2 were increased by day 7. By day 28, IL10, CCL2, CCL5, CXCL11, CTLA4, GZMB, IFN γ , CSF2, and IL6 were significantly increased. Therapeutic strategies involving TH1 induction and TH2 dampening may improve responses to immunotherapy.
机译:这项研究的目的是监测肿瘤植入后膀胱中免疫相关基因表达的变化。在第1天将小鼠原位植入MB49-PSA细胞(C57BL / 6小鼠),并在第7、14、21和28天终止。在第7天检查另一只小鼠模型(MBT-2 / C3H小鼠)。基因表达使用TaqMan低密度小鼠免疫组(Applied Biosystems,USA)对从膀胱中提取的RNA进行分析。通过实时PCR分析和RT-PCR对其他动物的mRNA再次确认所选基因。免疫抑制基因(IL13,IL1β,PTGS2,NOS2,IL10,CTLA4和CCL22)和免疫刺激基因(CSF2,GZMB,IFNγ,CXCL10,TNFα,CD80,IL12a和IL6)和AGTR2均升高到第28天,IL10,CCL2,CCL5,CXCL11,CTLA4,GZMB,IFNγ,CSF2和IL6显着增加。涉及TH1诱导和TH2抑制的治疗策略可能会改善对免疫疗法的反应。

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