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BK病毒诱导的骨肉瘤(Os515)作为人类骨肉瘤的模型。

BK virus-induced osteosarcoma (Os515) as a model of human osteosarcoma.

作者信息

Sekiguchi M, Miyazaki S, Fujikawa K, Shiroko Y, Asanuma K

机构信息

Department of Surgery I, Saitama Medical School, Japan.

出版信息

Anticancer Res. 1996 Jul-Aug;16(4A):1835-42.

PMID:8712710
Abstract

BK virus was isolated by Gardner et al in 1971 from the urine of an immunosuppressed patient with a kidney allograft. Antibodies to this virus are ubiquitous in the general populations worldwide, but the oncogenic capacity of BKV in humans had not been reported. The virus transformed in vitro permissive human and non-permissive animal cells, and the transformed cells had the T antigen. Intracerebral and intravenous inoculation of BKV in newborn hamsters induced malignant tumours (mainly ependymomas, malignant insulinomas, and osteosarcomas). Subcutaneous and intraperitoneal routes were also effective. The virus was only rescued from a few tumours by fusion with human embryonic cells or Vero cells. Brain tumours appeared earlier and osteosarcomas developed in animals which survived for more than 6 months. Many of the osteosarcomas were bony and grew slowly with frequent lung metastases, and a few osteosarcomas were soft and grew rapidly without lung metastases. Experimental targeting chemotherapy with doxorubicin (DX)-containing immunoliposomes was performed against Os515 osteosarcoma. In in vitro experiments, DX-Lip-MoAb29 showed a more significant inhibitory effect on cultured Os515 cells than free Dx and DX-Lip. DX-Lip DNP had less effect. In in vivo experiments, DX-Lip-MoAb29 suppressed the growth of Os515 tumour isografts in hamsters and prolonged the survival of recipients more significantly than free DX.

摘要

1971年,加德纳等人从一名接受肾移植的免疫抑制患者的尿液中分离出BK病毒。全世界普通人群中普遍存在针对这种病毒的抗体,但BK病毒在人类中的致癌能力此前尚未见报道。该病毒可在体外转化允许其生长的人类细胞和不允许其生长的动物细胞,且转化后的细胞含有T抗原。给新生仓鼠脑内和静脉接种BK病毒可诱发恶性肿瘤(主要是室管膜瘤、恶性胰岛素瘤和骨肉瘤)。皮下和腹腔注射途径也有效。只有通过与人胚胎细胞或非洲绿猴肾细胞融合,才能从少数肿瘤中拯救出该病毒。脑肿瘤出现较早,而在存活超过6个月的动物中会发生骨肉瘤。许多骨肉瘤为骨性,生长缓慢,常有肺转移,少数骨肉瘤质地柔软,生长迅速,无肺转移。针对Os515骨肉瘤进行了含阿霉素(DX)免疫脂质体的实验性靶向化疗。在体外实验中,DX-Lip-MoAb29对培养的Os515细胞的抑制作用比游离DX和DX-Lip更显著。DX-Lip DNP的作用较小。在体内实验中,DX-Lip-MoAb29抑制了仓鼠体内Os515肿瘤同基因移植瘤的生长,并且比游离DX更显著地延长了受体的生存期。

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