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Targeted Delivery of Secretory Promelittin via Novel Poly(lactone‐co‐β‐amino ester) Nanoparticles for Treatment of Breast Cancer Brain Metastases

机译:通过新型聚内酯-共-β-氨基酯类纳米颗粒靶向释放分泌型促泌素蛋白以治疗乳腺癌的脑转移

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摘要

Breast cancer brain metastases (BCBM) is a devastating disease with dismal prognosis. Although chemotherapy is widely used for clinical management of most tumors, it is often ineffective for BCBM. Therefore, alternative approaches for improved treatment of BCBM are in great demand. Here, an innovative gene therapy regimen is reported that is designed for effective treatment of BCBM. First, poly(lactone‐ ‐β‐amino ester) nanoparticles that are capable of efficient gene delivery are synthesized and are engineered for targeted delivery to BCBM through surface conjugation of AMD3100, which interacts with CXCR4 enriched in the tumor microenvironment. Next, an artificial gene, , is designed for the expression of secretory promelittin protein, which has limited toxicity on its own but releases cytolytic melittin after activation by MMP‐2 accumulated in tumors. It is demonstrated that delivery of the via the AMD3100‐conjugated nanoparticles effectively inhibits tumor progression in a BCBM mouse model. This study suggests a new direction to treat BCBM through targeted delivery of promelittin‐mediated gene therapy.
机译:乳腺癌脑转移瘤(BCBM)是一种破坏性疾病,预后不良。尽管化学疗法被广泛用于大多数肿瘤的临床治疗,但对BCBM常常无效。因此,迫切需要用于改善BCBM治疗的替代方法。在此,报道了设计用于有效治疗BCBM的创新基因治疗方案。首先,合成能够有效传递基因的聚(内酯-β-氨基酯)纳米粒子,并将其设计为通过AMD3100的表面缀合与肿瘤微环境中富集的CXCR4相互作用,靶向递送至BCBM。接下来,设计了一个人工基因,用于表达分泌型催乳素蛋白,该蛋白本身具有有限的毒性,但在肿瘤中积累的MMP-2激活后会释放细胞溶解性蜂毒素。事实证明,通过共轭AMD3100的纳米颗粒传递BCBM小鼠模型可有效抑制肿瘤进展。这项研究提出了通过有针对性地进行前激肽介导的基因治疗来治疗BCBM的新方向。

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