Nanobubble-mediated co-delivery of siTRIM37 and IR780 for gene and sonodynamic combination therapy against triple negative breast cancer.

Xiang He, Shentao Zhang, Yuhang Tian, Jialin Dong, Yanchi Yuan, Hui Jing
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Abstract

Gene therapy often fails due to enzyme degradation and low transfection efficiency, and single gene therapy usually cannot completely kill tumor cells. Several studies have reported that tripartite motif-containing protein 37 (TRIM37) plays a significant role in promoting the occurrence and development of triple negative breast cancer (TNBC). Herein, we constructed siTRIM37 and IR780 co-loaded nanobubbles (NBs) to achieve the combination of gene therapy and sonodynamic therapy (SDT) against TNBC. On the one hand, ultrasound irradiation causes siRNA@IR780 NBs rupture to produce ultrasound targeted NB destruction effect, which promotes the entry of IR780 and siTRIM37 into cells, increasing the local concentration of IR780 and gene transfection efficiency. On the other hand, under the stimulation of ultrasound, IR780 generates reactive oxygen species to kill TNBC cells. Mechanism studies reveal that TRIM37 is an anti-apoptotic gene in TNBC, and inhibiting TRIM37 expression can induce cell death through the apoptotic pathway. And the combination of siTRIM37 and SDT can aggravate the degree of apoptosis to increase cell death. Therefore, siRNA@IR780 NBs-mediated combination therapy may provide a new treatment approach for TNBC in the future.

纳米气泡介导的 siTRIM37 和 IR780 联合给药,用于基因和声动力联合疗法治疗三阴性乳腺癌。
基因治疗往往因酶降解和转染效率低而失败,单一基因治疗通常不能完全杀死肿瘤细胞。多项研究表明,TRIM37在三阴性乳腺癌(TNBC)的发生和发展中起着重要的促进作用。在此,我们构建了siTRIM37和IR780共同负载的纳米气泡(NBs),以实现基因治疗和声动力治疗(SDT)对TNBC的结合。一方面,超声辐照使siRNA@IR780纳米气泡破裂,产生超声靶向纳米气泡破坏效应(UTND),促进IR780和siTRIM37进入细胞,提高IR780的局部浓度和基因转染效率。另一方面,在超声波的刺激下,IR780 会产生活性氧(ROS),从而杀死 TNBC 细胞。机理研究发现,TRIM37是TNBC的抗凋亡基因,抑制TRIM37的表达可通过凋亡途径诱导细胞死亡。而 siTRIM37 与 SDT 联用可加重细胞凋亡程度,增加细胞死亡。因此,siRNA@IR780 NBs介导的联合疗法可能会在未来为TNBC提供一种新的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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