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溶瘤细小病毒的临床前测试:标准细小病毒 H-1PV 有效诱导骨肉瘤细胞体外裂解。

Preclinical Testing of an Oncolytic Parvovirus: Standard Protoparvovirus H-1PV Efficiently Induces Osteosarcoma Cell Lysis In Vitro.

机构信息

Division of Tumor Virology, Program Infection, Inflammation and Cancer, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 242, 69120 Heidelberg, Germany.

Department of Bioengineering, Imperial College, London W7 2AZ, UK.

出版信息

Viruses. 2017 Oct 17;9(10):301. doi: 10.3390/v9100301.

Abstract

Osteosarcoma is the most frequent malignant disease of the bone. On the basis of early clinical experience in the 1960s with H-1 protoparvovirus (H-1PV) in osteosarcoma patients, this effective oncolytic virus was selected for systematic preclinical testing on various osteosarcoma cell cultures. A panel of five human osteosarcoma cell lines (CAL 72, H-OS, MG-63, SaOS-2, U-2OS) was tested. Virus oncoselectivity was confirmed by infecting non-malignant human neonatal fibroblasts and osteoblasts used as culture models of non-transformed mesenchymal cells. H-1PV was found to enter osteosarcoma cells and to induce viral DNA replication, transcription of viral genes, and translation to viral proteins. After H-1PV infection, release of infectious viral particles from osteosarcoma cells into the supernatant indicated successful viral assembly and egress. Crystal violet staining revealed progressive cytomorphological changes in all osteosarcoma cell lines. Infection of osteosarcoma cell lines with the standard H-1PV caused an arrest of the cell cycle in the G2 phase, and these lines had a limited capacity for standard H-1PV virus replication. The cytotoxicity of wild-type H-1PV virus towards osteosarcoma cells was compared in vitro with that of two variants, Del H-1PV and DM H-1PV, previously described as fitness variants displaying higher infectivity and spreading in human transformed cell lines of different origins. Surprisingly, wild-type H-1PV displayed the strongest cytostatic and cytotoxic effects in this analysis and thus seems the most promising for the next preclinical validation steps in vivo.

摘要

骨肉瘤是最常见的骨恶性疾病。基于 20 世纪 60 年代在骨肉瘤患者中使用 H-1 细小病毒(H-1PV)的早期临床经验,选择了这种有效的溶瘤病毒,对各种骨肉瘤细胞培养物进行了系统的临床前测试。对一组五个人骨肉瘤细胞系(CAL 72、H-OS、MG-63、SaOS-2、U-2OS)进行了测试。通过感染非恶性的人胎儿成纤维细胞和作为未转化间充质细胞培养模型的成骨细胞,证实了病毒的肿瘤选择性。发现 H-1PV 进入骨肉瘤细胞,并诱导病毒 DNA 复制、病毒基因转录和翻译为病毒蛋白。H-1PV 感染后,从骨肉瘤细胞中释放出感染性病毒颗粒到上清液中,表明病毒成功组装和出芽。结晶紫染色显示所有骨肉瘤细胞系都出现了进行性的细胞形态学变化。标准 H-1PV 感染骨肉瘤细胞系会导致细胞周期在 G2 期停滞,这些细胞系对标准 H-1PV 病毒复制的能力有限。在体外,野生型 H-1PV 对骨肉瘤细胞的细胞毒性与两种变体(Del H-1PV 和 DM H-1PV)进行了比较,这两种变体之前被描述为具有更高感染性和在不同来源的人转化细胞系中传播的适应性变体。令人惊讶的是,野生型 H-1PV 在这项分析中表现出最强的细胞抑制和细胞毒性作用,因此在体内进行下一步临床前验证步骤似乎最有前途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fd1/5691652/760e6f50a2da/viruses-09-00301-g001.jpg

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