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Human papillomavirus type 16 E6 and E 7 proteins alter NF-kB in cultured cervical epithelial cells and inhibition of NF-kB promotes cell growth and immortalization

机译:人乳头瘤病毒16型E6和E 7蛋白改变培养的宫颈上皮细胞中的NF-kB,抑制NF-kB促进细胞生长和永生化

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摘要

The NF-kB family of transcription factors regulates important biological functions including cell growth, survival and the immune response. We found that Human Papillomavirus type 16 (HPV-16) E7 and E6/E7 proteins inhibited basal and TNF-alpha-inducible NF-kB activity in human epithelial cells cultured from the cervical transformation zone, the anatomic region where most cervical cancers develop. In contrast, HPV-16 E6 regulated NF-kB in a cell type- and cell growth-dependent manner. NF-kB influenced immortalization of cervical cells by HPV16. Inhibition of NF-kB by an IkB alpha repressor mutant increased colony formation and immortalization by HPV-16. In contrast, activation of NF-kB by constitutive expression of p65 inhibited proliferation and immortalization. Our results suggest that inhibition of NF-kB by HPV-16 E6/E7 contributes to immortalization of cells from the cervical transformation zone.
机译:NF-kB转录因子家族调节重要的生物学功能,包括细胞生长,存活和免疫反应。我们发现人乳头瘤病毒16型(HPV-16)E7和E6 / E7蛋白抑制从宫颈转化区(大多数宫颈癌发生的解剖区域)培养的人上皮细胞的基础和TNF-α诱导的NF-kB活性。相反,HPV-16 E6以细胞类型和细胞生长依赖性方式调节NF-kB。 NF-kB通过HPV16影响宫颈细胞的永生化。 IkBα阻遏物突变体对NF-kB的抑制作用会增加菌落的形成,并通过HPV-16永生。相反,通过p65的组成型表达激活NF-kB抑制了增殖和永生化。我们的结果表明,HPV-16 E6 / E7对NF-kB的抑制作用有助于使宫颈转化区的细胞永生化。

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