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Effects of intravesical therapy with platelet-rich plasma (PRP) and Bacillus Calmette-Guerin (BCG) in non-muscle invasive bladder cancer

机译:富含血小板血浆(PRP)和芽孢杆菌秃牛癌(BCG)的膀胱内疗法对非肌肉侵袭性膀胱癌的影响

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摘要

This study describes the effects of a promising therapeutic alternative for non-muscle invasive bladder cancer (NMIBC) based on Bacillus Calmette-Guerin (BCG) intravesical immunotherapy combined with Platelet-rich plasma (PRP) in an animal model. Furthermore, this study describes the possible mechanisms of this therapeutic combination involving Toll-like Receptors (TLRs) 2 and 4 signaling pathways. NMIBC was induced by treating female Fischer 344 rats with N-methyl-N-nitrosourea (MNU). After treatment with MNU, the animals were distributed into four experimental groups: Control (without MNU) group, MNU (cancer) group, MNU + PRP group, MNU + BCG group and MNU + PRP + BCG group. Our results demonstrated that PRP treatment alone or associated with BCG triggered significant cytotoxicity in bladder carcinoma cells (HTB-9). Animals treated with PRP associated to BCG clearly showed better histopathological recovery from the cancer state and decrease of urothelial neoplastic lesions progression in 70% of animals when compared to groups that received the same therapies administered singly. In addition, this therapeutic association led to distinct activation of immune system TLRs 2 and 4-mediated, resulting in increased MyD88, TRIF, IRF3, IFN-gamma immunoreactivities. Taken together, the data obtained suggest that interferon signaling pathway activation by PRP treatment in combination with BCG immunotherapy may provide novel therapeutic approaches for non-muscle invasive bladder cancer.
机译:本研究描述了对非肌肉侵袭性膀胱癌(NMIBC)基于Bacillus Calmette-guerin(BCG)膀胱内免疫治疗的疗效与动物模型中的富含血小板的血浆(PRP)的影响。此外,该研究描述了这种治疗组合的可能机制,涉及涉及的受体(TLRS)2和4信号通路。通过用N-甲基-N-硝基脲(MNU)处理雌性费氏344大鼠诱导NMIBC。在用MNU治疗后,将动物分发给四组:对照(没有MNU)组,MNU(癌症)组,MNU + PRP组,MNU + BCG组和MNU + PRP + BCG组。我们的结果表明,单独的PRP处理或与BCG相关的治疗在膀胱癌细胞(HTB-9)中引发了显着的细胞毒性。与BCG相关的PRP治疗的动物清楚地表明,与接受单独施用相同疗法的组的组,70%动物的尿路上肿瘤病变减少更好地显示出更好的组织病理学回收。此外,这种治疗功能导致免疫系统TLR 2和4介导的不同激活,导致MyD88,TRIF,IRF3,IFN-Gamma免疫反应增加。所获得的数据表明,PRP治疗与BCG免疫疗法组合的干扰素信号通路激活可以为非肌肉侵入性膀胱癌提供新的治疗方法。

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