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使用微泡进行的表皮生长因子受体靶向性超声穿孔增强了鳞状细胞癌模型中的治疗效果。

Epidermal growth factor receptor-targeted sonoporation with microbubbles enhances therapeutic efficacy in a squamous cell carcinoma model.

作者信息

Hirabayashi Fumika, Iwanaga Kenjiro, Okinaga Toshinori, Takahashi Osamu, Ariyoshi Wataru, Suzuki Ryo, Sugii Mutsumi, Maruyama Kazuo, Tominaga Kazuhiro, Nishihara Tatsuji

机构信息

Division of Infections and Molecular Biology, Department of Health Promotion, Kyushu Dental University, Kitakyushu, Japan.

Division of Oral and Maxillofacial Surgery, Department of Science of Physical Functions, Kyushu Dental University, Kitakyushu, Japan.

出版信息

PLoS One. 2017 Sep 22;12(9):e0185293. doi: 10.1371/journal.pone.0185293. eCollection 2017.

Abstract

Sonoporation is a drug and gene delivery system using ultrasonication that allows the intracellular delivery of foreign molecules that cannot enter cells under normal conditions. We previously reported that sonoporation with microbubbles (MBs) could achieve effective intracellular drug delivery to human gingival squamous carcinoma Ca9-22 cells. In this study, we developed anti-epidermal growth factor receptor (EGFR) antibody-conjugated MBs (EGFR-MBs) and evaluated their capacity to enhance anti-cancer drug toxicity in vitro and in vivo. We first assessed the effect of sonoporation with EGFR-MBs on Ca9-22 cells by the WST-8 assay, flow cytometry and Hoechst's staining in vitro. Sonoporation and EGFR-MB had a strong cytotoxic effect on Ca9-22 cells with low-dose bleomycin. Furthermore, bleomycin delivery using sonoporation with EGFR-MBs remarkably increased the number of apoptotic cells. We next examined the effect of EGFR-MBs in a murine squamous cell carcinoma model. Bleomycin delivery by sonoporation with EGFR-MBs exhibited remarkable antitumor activity. Together, our results show that EGFR-MBs and ultrasound treatment increases the efficacy and specificity of intracellular drug uptake, suggesting this could be a novel drug-targeting modality for oral squamous cell carcinoma chemotherapy treatment.

摘要

超声穿孔是一种利用超声处理的药物和基因递送系统,它能够使在正常条件下无法进入细胞的外来分子实现细胞内递送。我们之前报道过,微泡(MBs)介导的超声穿孔能够有效地将药物递送至人牙龈鳞状癌细胞Ca9-22内。在本研究中,我们制备了抗表皮生长因子受体(EGFR)抗体偶联的微泡(EGFR-MBs),并评估了其在体外和体内增强抗癌药物毒性的能力。我们首先通过WST-8检测、流式细胞术和体外Hoechst染色评估了EGFR-MBs介导的超声穿孔对Ca9-22细胞的影响。超声穿孔和EGFR-MB对低剂量博来霉素处理的Ca9-22细胞具有很强的细胞毒性作用。此外,EGFR-MBs介导的超声穿孔递送博来霉素显著增加了凋亡细胞的数量。接下来,我们在小鼠鳞状细胞癌模型中研究了EGFR-MBs的作用。EGFR-MBs介导的超声穿孔递送博来霉素表现出显著的抗肿瘤活性。总之,我们的结果表明,EGFR-MBs和超声处理提高了细胞内药物摄取的疗效和特异性,提示这可能是口腔鳞状细胞癌化疗治疗的一种新型药物靶向方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432c/5609770/a298d8566102/pone.0185293.g001.jpg

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