首页> 外文期刊>Journal of immunology research. >Tumor and Microenvironment Modification during Progression of Murine Orthotopic Bladder Cancer
【24h】

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

获取原文
           

摘要

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, IL1β, PTGS2, NOS2, IL10, CTLA4, and CCL22) and immune stimulatory genes (CSF2, GZMB, IFNγ, CXCL10, TNFα, CD80, IL12a, and IL6) and AGTR2 were increased by day 7. By day 28, IL10, CCL2, CCL5, CXCL11, CTLA4, GZMB, IFNγ, 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(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在第7天增加。在图28中,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。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号