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Mechanism responsible for the antitumor effect of BCG-CWS using the LEEL method in a mouse bladder cancer model

机译:使用LEEL方法在小鼠膀胱癌模型中负责BCG-CWS抗肿瘤作用的机制

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摘要

We previously reported on the development of a water soluble formulation of the cell wall skeleton of BCG (BCG-CWS), a major immune active center of BCG, by encapsulating it into a nanoparticle (CWS-NP). The CWS-NP allowed us to clarify the machinery associated with the BCG mediated anti-bladder tumor effect, especially the roles of bladder cancer cells and dendritic cells (DCs) in the initial step, which remains poorly understood. We show herein that the internalization of BCG-CWS by bladder cancer cells, but not DCs, is indispensable for the induction of an antitumor effect against bladder cancer. Tumor growth was significantly inhibited in mice that had been inoculated with mouse bladder cancer (MBT-2) cells containing internalized BCG-CWS. On the other hand, the internalization of BCG-CWS by DCs had only a minor effect on inducing an antitumor effect against MBT-2 tumors. This was clarified for the first time by using the CWS-NP. This finding provides insights into our understanding of the role of bladder cancer cells and DCs in BCG therapy against bladder cancer. (C) 2014 Elsevier B.V. All rights reserved.
机译:我们之前曾报道过将BCG的细胞壁骨架(BCG-CWS)(一种BCG的主要免疫活性中心)封装到纳米颗粒(CWS-NP)中的水溶性制剂的开发。 CWS-NP使我们能够阐明与BCG介导的抗膀胱肿瘤作用相关的机制,尤其是在最初阶段中膀胱癌细胞和树突状细胞(DC)的作用,至今仍知之甚少。我们在这里表明,膀胱癌细胞对BCG-CWS的内在化,而不是DC,对于诱导针对膀胱癌的抗肿瘤作用是必不可少的。在用含有内在的BCG-CWS的小鼠膀胱癌(MBT-2)细胞接种的小鼠中,肿瘤的生长受到显着抑制。另一方面,DCs对BCG-CWS的内在化在诱导针对MBT-2肿瘤的抗肿瘤作用方面只具有很小的作用。这是使用CWS-NP首次澄清的。这一发现为我们对膀胱癌细胞和DC在BCG治疗膀胱癌中的作用的理解提供了见识。 (C)2014 Elsevier B.V.保留所有权利。

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