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转染诱导的肿瘤坏死因子-α对皮下移植的人胶质瘤的生长抑制作用及γ-干扰素对其作用的增强

Growth inhibition of subcutaneously transplanted human glioma by transfection-induced tumor necrosis factor-alpha and augmentation of the effect by gamma-interferon.

作者信息

Harada K, Yoshida J, Mizuno M, Sugita K, Kurisu K, Uozumi T

机构信息

Department of Neurosurgery, Nagoya University School of Medicine, Japan.

出版信息

J Neurooncol. 1994;22(3):221-5. doi: 10.1007/BF01052922.

Abstract

Using subcutaneous solid tumors produced by U251-MG human glioma cells, we studied the in vivo transfection of the cells with the tumor necrosis factor-alpha (TNF-alpha) gene delivered by means of liposomes. When the tumor had become 7 mm in diameter, liposomes with entrapped TNF-alpha gene were injected into the center of the subcutaneous tumor. We found that mRNA of transfection-induced TNF-alpha, which was expressed in the tumor tissue, was detected by reverse transcriptase-polymerase chain reaction (RT-PCR) method and its protein was demonstrated by enzyme-linked immunoassay. Growth of the tumor was inhibited when the injection was carried out five times at every other day. The growth-inhibitory effect by transfection-induced TNF-alpha was much remarkable as compared with exogenous TNF-alpha and the effect was enhanced by the intraperitoneal injection of gamma-interferon (IFN-gamma) 12 h prior to intratumoral injection of the liposomes.

摘要

利用U251-MG人胶质瘤细胞产生的皮下实体瘤,我们研究了通过脂质体递送肿瘤坏死因子-α(TNF-α)基因对细胞进行体内转染的情况。当肿瘤直径达到7毫米时,将包裹有TNF-α基因的脂质体注射到皮下肿瘤的中心。我们发现,通过逆转录聚合酶链反应(RT-PCR)方法在肿瘤组织中检测到了转染诱导的TNF-α的mRNA,并且通过酶联免疫测定法证实了其蛋白质的存在。每隔一天进行5次注射时,肿瘤生长受到抑制。与外源性TNF-α相比,转染诱导的TNF-α的生长抑制作用更为显著,并且在瘤内注射脂质体前12小时腹腔注射γ-干扰素(IFN-γ)可增强该作用。

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