Yamaguchi Taiki, Endo-Takahashi Yoko, Amano Takumi, Ihara Arina, Sakuma Tetsushi, Yamamoto Takashi, Fukazawa Takuya, Negishi Yoichi
Department of Drug Delivery and Molecular Biopharmaceutics, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji 192-0392, Tokyo, Japan.
Laboratory of Genome Editing Breeding, Graduate School of Agriculture, Kyoto University, 448-5 Kajiicho, Kamigyo-ku, Kyoto-shi 602-0841, Kyoto, Japan.
Pharmaceutics. 2025 Aug 13;17(8):1053. doi: 10.3390/pharmaceutics17081053.
: Lung squamous cell carcinoma (SCC), a major subtype of non-small cell lung cancer, remains a significant clinical challenge due to a scarcity of actionable molecular targets and the limited effectiveness of current targeted therapies. Emerging treatment strategies inhibit the gene expression of lineage survival oncogenes such as ΔNp63 and SOX2. CRISPR interference (CRISPRi) is a promising method to downregulate these genes; however, the efficacy depends on effective delivery. Here, we focused on the delivery system using nanobubbles (NBs) and ultrasound (US) for site-specific CRISPRi delivery to SCC. We evaluated the therapeutic efficacy of plasmid-based CRISPRi (pCRISPRi) targeting SOX2 or ΔNp63 using intratumoral pCRISPRi/NBs injections followed by US. : A mixture of NBs and pCRISPRi was injected directly into the tumors and exposed to US-induced cavitation to facilitate pCRISPRi uptake. Tumor volume was measured every other day, and apoptosis was assessed by TUNEL assay. : In a lung SCC xenograft model, NBs/US-mediated pCRISPRi delivery induced apoptosis and significantly suppressed tumor growth. : These findings suggest that US-guided, NB-facilitated delivery of pCRISPRi can locally suppress lineage survival oncogenes and trigger tumor cell death, representing a promising targeted therapy for lung SCC. Additionally, this platform could be adapted to other cancers by targeting alternative factors.
肺鳞状细胞癌(SCC)是非小细胞肺癌的主要亚型,由于缺乏可操作的分子靶点以及当前靶向治疗效果有限,它仍然是一个重大的临床挑战。新兴的治疗策略可抑制诸如ΔNp63和SOX2等谱系存活癌基因的基因表达。CRISPR干扰(CRISPRi)是一种下调这些基因的有前景的方法;然而,其疗效取决于有效的递送。在此,我们聚焦于使用纳米气泡(NBs)和超声(US)的递送系统,用于将CRISPRi位点特异性递送至SCC。我们通过瘤内注射pCRISPRi/NBs并随后进行超声处理,评估了靶向SOX2或ΔNp63的基于质粒的CRISPRi(pCRISPRi)的治疗效果。将NBs和pCRISPRi的混合物直接注射到肿瘤中,并使其暴露于超声诱导的空化作用以促进pCRISPRi的摄取。每隔一天测量肿瘤体积,并通过TUNEL测定法评估细胞凋亡。在肺SCC异种移植模型中,NBs/US介导的pCRISPRi递送诱导了细胞凋亡并显著抑制了肿瘤生长。这些发现表明,超声引导、NBs促进的pCRISPRi递送可局部抑制谱系存活癌基因并触发肿瘤细胞死亡,这代表了一种有前景的肺SCC靶向治疗方法。此外,通过靶向其他因子,该平台可适用于其他癌症。