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作 者:沈历宗[1] 王建华[1] 王海权[1] 吴文溪[1]
机构地区:[1]南京医科大学第一附属医院普通外科,210029
出 处:《中华普通外科杂志》2006年第11期819-821,共3页Chinese Journal of General Surgery
基 金:江苏省高校自然科学基金资助项目(03KD320140)
摘 要:目的研究人γ-干扰素(human interferon-γ,huIFN-γ)基因修饰的结肠癌细胞瘤苗的成瘤性及抗肿瘤作用。方法用逆转录病毒质粒pL(IFN-γ)SN将人IFN-γ基因转导入鼠结肠癌细胞株CT26中,用G418进行筛选,得到抗性克隆CT26/IFN-γ,比较CT26/IFN-γ与野生型CT26的成瘤性,评价CT26/IFN-γ对野生型CT26细胞肝转移模型的治疗作用。结果CT26/IFN-γ能在含0.6 g·L-1 G418的培养液中稳定生长;RT-PCR证实IFN-γ基因在CT26/IFN-γ中表达;CT26/IFN-γ细胞能分泌人IFN-γ,体外培养体系中产量为3.5 fg·cell-1·d-1;CT26/IFN-γ的成瘤性比野生型CT26差[Balb/c小鼠肿瘤体积分别为(480±138)mm3与(991±176)mm3,F=31.29,P=0.000]; CT26/IFN-γ对野生型CT26的肝转移亦有明显抑制作用,荷瘤小鼠存活期明显延长(P=0.000)。结论人IFN-γ基因修饰的结肠癌细胞瘤苗有一定的抗肿瘤作用,值得进行深入研究。Objective To investigate the anti-tumor effect of colon cancer cell vaccine modified by human interferon-γ. Methods A murine colon cancer cell vaccine CT26/IFN-γ was established by gene modification using retrovirus plasmid pL(IFN-γ) SN, the tumorigenicity and effect of the cancer cell vaccine on colon cancer liver metastasis model was evaluated. Results CT26/IFN-γ was established successfully. It grows stably in a medium containing 0. 6 g · L^-1 G418. IFN-γ gene expression in this mutant was confirmed by RT-PCR. This mutant secreted huIFN-γ with a yield of 3.5 fg · cell^ - 1 γ· d ^- 1 in cultured medium. The volume of tumors from this mutant (480 ± 138 mm^3 ) was less than that from wild-type one (991 ± 176 mm^3 , F = 31.29, P = 0. 000 ) when tumor cells were inoculated into a Balb/c mouse model subcutaneously. CT26/IFN-γ impeded tumor progress and prolonged the survival time in CT26 cell liver metastasis model ( P = 0. 000 ). Conclusion The murine colon cancer cell vaccine modified by human interferon-γ presents anti-tumor effect to some extent.
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