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干扰素调节因子-1基因异常与α干扰素对人肝癌细胞系生长抑制作用的丧失

Interferon regulatory factor-1 gene abnormality and loss of growth inhibitory effect of interferon-alpha in human hepatoma cell lines.

作者信息

Tada S, Saito H, Tsunematsu S, Ebinuma H, Wakabayashi K, Masuda T, Ishii H

机构信息

Department of Internal Medicine, School of Medicine, Keio University, Tokyo 160, Japan.

出版信息

Int J Oncol. 1998 Dec;13(6):1207-16. doi: 10.3892/ijo.13.6.1207.

Abstract

The effect of IFN-alpha on the growth of 5 hepatoma cell lines and a normal liver-derived cell line were examined. IFN dose-dependently inhibited the growth of cell lines except for HLE and PLC/PRF/5 in which the inhibition only occurred at a high concentration over 10,000 IU/ml. IFN-alpha induced the G1 arrest of these cells according to upregulation of p21WAF-1 expression, which is induced in PLC/PRF/5 and HLE only at a high IFN concentration. The receptor for IFN-alpha was well expressed in all the cell lines. DNA rearrangement of IRF-1 was detected in HLE and PLC/PRF/5 by Southern blotting, while IRF-2 gene was preserved. IFN-induced gene expressions were compared between HCC-T, HCC-M and PLC/PRF/5. RT-PCR demonstrated that the full-length IRF-1 and -2 mRNA was transcribed in all cell lines, but the mRNA amount of former gene in PLC/PRF/5 was less than that in HCC-T and HCC-M, about 1/10 by competitive RT-PCR. The sequence analysis of IRF-1 cDNA was performed and the full-length mRNA transcription was reconfirmed in PLC/PRF/5, but no significant point mutation was detected. These results suggest that IFN-alpha inhibits hepatoma growth by increasing p21WAF-1 expression only when the IRF-1 gene is preserved normally.

摘要

研究了干扰素-α(IFN-α)对5种肝癌细胞系和1种正常肝源细胞系生长的影响。IFN呈剂量依赖性抑制各细胞系的生长,但HLE和PLC/PRF/5细胞系除外,这两种细胞系仅在IFN浓度超过10000 IU/ml的高浓度时才出现生长抑制。IFN-α通过上调p21WAF-1的表达诱导这些细胞的G1期阻滞,而p21WAF-1仅在高浓度IFN作用下在PLC/PRF/5和HLE细胞系中被诱导表达。IFN-α受体在所有细胞系中均有良好表达。通过Southern印迹法在HLE和PLC/PRF/5细胞系中检测到IRF-1的DNA重排,而IRF-2基因保持完整。比较了HCC-T、HCC-M和PLC/PRF/5细胞系中IFN诱导的基因表达。逆转录-聚合酶链反应(RT-PCR)显示,所有细胞系均转录了全长的IRF-1和-2 mRNA,但PLC/PRF/5细胞系中前一个基因的mRNA量低于HCC-T和HCC-M细胞系,通过竞争性RT-PCR检测约为后者的1/10。对IRF-1 cDNA进行了序列分析,并在PLC/PRF/5细胞系中再次证实了全长mRNA的转录,但未检测到明显的点突变。这些结果表明,仅当IRF-1基因正常保存时,IFN-α才通过增加p21WAF-1的表达来抑制肝癌生长。

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