小鼠疱疹病毒68 (MHV-68)相关生长因子68 (MHGF-68)对胸腺裸鼠肿瘤进展的影响

M. Šupolíková, M. Labudova, E. Nováková, A. Staňová, V. Šišovský, F. Golais
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引用次数: 1

摘要

在本研究中,MHV-68相关生长因子68 (MHGF-68)在不同纯化阶段和不同化学方法处理的馏分中对肿瘤生长的开始和进展的影响进行了论证。以感染鼠疱疹病毒68 (Murine herpesvirus 68, MHV-68)的BHK-21细胞为培养基,采用常规化学方法(去离子水和生理溶液pH 7.2稀释,正丁醇和氯仿离心提取)和不同的层析技术对生物样品进行分离。所有得到的组分都进行了生物活性测试。实验选用4周龄胸腺裸小鼠,皮下感染肿瘤Hepa 1c1c7细胞悬液。给药后8 d内观察肿瘤增殖。随后静脉注射具有抗增殖作用的MHGF-68组分1B1和1D2进行体内实验,观察其对小鼠肿瘤生长的开始或进展的抑制活性。与对照小鼠相比,用MHGF-68组分处理的实验小鼠肿瘤表现出肿瘤生长减少。这些数据表明,用MHGF-68的1B1和1D2部分治疗后,肿瘤异种移植物受到抑制。综上所述,MHGF-68在调节肿瘤生长方面的潜力可以作为开发具有抗增殖作用的新型癌症治疗措施的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Murine Herpesvirus 68 (MHV-68) Related Growth Factor 68 (MHGF-68) on the Tumor Progression in Athymic Nude Mice
In this study the effect of MHV-68 related growth factor 68 (MHGF-68) on initiation and progression of tumor growth using fractions in various stages of purification and treated with various chemical methods was demonstrated. The biological sample in the form of culture medium of BHK-21 cells infected with Murine herpesvirus 68 (MHV-68) was fractionated using conventional chemical procedures (dilution by deionized water and physiological solution pH 7.2, centrifugation and extraction with n-butanol and chloroform) and different chromatographic techniques. All obtained fractions were tested for biological activity. In the experiments were used 4 weeks old athymic nude mice, subcutaneously infected with the suspension of tumor Hepa 1c1c7 cells. Within 8 days post administration tumor proliferation was observed. Subsequently intravenously administered MHGF-68 fractions 1B1 and 1D2 with the antiproliferative effect were tested in vivo to see their inhibitory activity on the initiation or progression of tumor growth in mice. Tumors in experimental mice treated with MHGF-68 fractions exhibited decreased growth of tumors in comparison to control mice. These data show that tumor xenografts were suppressed after treatment with 1B1 and 1D2 fractions of MHGF-68. Taken together, the promising potential of MHGF-68 in modulating tumor growth could be used as a foundation for development of novel cancer treatment measures with antiproliferative effects.
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