Department of Ultrasound, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150081, People's Republic of China.
Biomed Mater. 2024 Oct 1;19(6). doi: 10.1088/1748-605X/ad7e6d.
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.
基因治疗常因酶降解和转染效率低而失败,而单一的基因治疗通常不能完全杀死肿瘤细胞。有几项研究报道,三结构域蛋白 37(TRIM37)在促进三阴性乳腺癌(TNBC)的发生和发展中起重要作用。在此,我们构建了 siTRIM37 和 IR780 共载纳米泡(NBs),以实现针对 TNBC 的基因治疗和声动力学治疗(SDT)的联合。一方面,超声辐照导致 siRNA@IR780 NBs 破裂,产生超声靶向 NB 破坏效应,促进 IR780 和 siTRIM37 进入细胞,增加 IR780 的局部浓度和基因转染效率。另一方面,在超声的刺激下,IR780 产生活性氧杀死 TNBC 细胞。机制研究表明,TRIM37 是 TNBC 中的一种抗凋亡基因,抑制 TRIM37 表达可以通过凋亡途径诱导细胞死亡。siTRIM37 和 SDT 的联合治疗可以加重细胞凋亡程度,增加细胞死亡。因此,siRNA@IR780 NBs 介导的联合治疗可能为未来的 TNBC 提供一种新的治疗方法。