首页> 外文期刊>Molecular cancer therapeutics >Sentinel Lymph Node-Targeted Therapy by Oncolytic Sendai Virus Suppresses Micrometastasis of Head and Neck Squamous Cell Carcinoma in an Orthotopic Nude Mouse Model
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Sentinel Lymph Node-Targeted Therapy by Oncolytic Sendai Virus Suppresses Micrometastasis of Head and Neck Squamous Cell Carcinoma in an Orthotopic Nude Mouse Model

机译:Sentinel淋巴结靶向治疗肉瘤仙奈语病毒在原位裸鼠模型中抑制了头颈鳞状细胞癌的微转移

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In clinical NO (cNO) cases with head and neck squamous cell carcinoma (HNSCC), a treatment selection is still controversial: elective neck dissection or watchful waiting. We focused on sentinel lymph node (SLN)-targeted therapy using the urokinase-type plasminogen activator (uPA)-dependent oncolytic Sendai virus "BioKnife." The objectives of this study were to investigate BioKnife migration into SLNs and elucidate its antitumor effect on lymph node metastases (LNM). We established an orthotopic nude mouse model of HNSCC, with LNM being frequently induced. We inoculated HSC-3-M3, human highly metastatic tongue squamous cell carcinoma cells, in the tongue of the nude mice, and after 2 weeks, we injected BioKnife into the primary tumor. We tracked BioKnife migration into the SLNs by immunostaining, RT-PCR, and an in vivo imaging system. We also examined its antitumor effects and mechanisms through serial section analysis of lymph nodes. GFP reporter expression was dearly visible in the lymph nodes of virus groups, which corresponded to SLNs. Relative GFP mRNA was significantly increased in both the tongues and lymph nodes in the virus groups compared with that in the control group (P < 0.05). Serial section analysis showed that BioKnife infected cancer cells and exhibited significant antitumor effect against LNM compared with the control groups (P < 0.05). We detected apoptosis in LNM infected by BioKnife. BioKnife migrated into SLNs after its injection into the primary tumor and effectively suppressed LNM, suggesting that SLN-targeted therapy using BioKnife has great potential to provide a novel and promising alternative to elective neck dissection in cNO patients with HNSCC.
机译:在临床NO(CNO)病例中,头颈鳞状细胞癌(HNSCC),治疗选择仍然存在争议:选修颈部解剖或手表等待。我们专注于使用尿激酶型纤溶酶原激活剂(UPA) - 依赖于孤立溶解玉米菌仙台病毒“Bioknife”的Sentinel淋巴结(SLN)治疗。本研究的目标是将Bioknife迁移调查到SLNS中,并阐明其对淋巴结转移(LNM)的抗肿瘤作用。我们建立了HNSCC的原位裸鼠模型,经常诱导LNM。我们接种HSC-3-M3,人高度转移性舌鳞状细胞癌细胞,在裸鼠的舌头,2周后,我们将Bioknife注入原发性肿瘤。我们通过免疫染色,RT-PCR和体内成像系统跟踪BIoknife迁移到SLN中。我们还通过淋巴结分析检查其抗肿瘤效应和机制。 GFP报告者表达在病毒组的淋巴结中是可见的,其对应于SLNS。与对照组中的病毒组中的舌片和淋巴结两者相对GFP mRNA显着增加(P <0.05)。序列截面分析表明,与对照组相比,博伊霍伊弗受到癌细胞并表现出对LNM的显着抗肿瘤效应(P <0.05)。我们检测到Bioknife感染的LNM中的细胞凋亡。在注射到原发性肿瘤并有效地抑制LNM后,Bioknife迁移到SLN中,表明使用Bioknife的SLN靶向治疗具有很大的潜力,可以提供一种新颖的和有前途的替代CNO患者HNSCC患者的选修颈部解剖。

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