山东大学学报 (医学版) ›› 2018, Vol. 56 ›› Issue (12): 1-6.doi: 10.6040/j.issn.1671-7554.0.2018.369
• 基础医学 •
张文浩1,2,乔立君2,郑静怡1,陈健行2,张魏芳1
ZHANG Wenhao1,2, QIAO Lijun2, ZHENG Jingyi1, Jason Chen2, ZHANG Weifang1
摘要: 目的 探究人乳头瘤病毒(HPV)编码的早期癌蛋白E6/E7对小GTP酶蛋白Rab12表达的影响。 方法 利用逆转录病毒包装系统获得含pBabe-Vector质粒和pBabe-16E7质粒的高滴度病毒颗粒,感染细胞,并用嘌呤霉素筛选获得稳定表达HPV16E7的UMSCC 10A-16E7细胞系,Western blotting检测E7相关蛋白p53和E2F1的表达变化,比较UMSCC 10A-Vector细胞系和UMSCC 10A-16E7细胞系的Rab12蛋白表达水平。用同样方法在HaCaT、RPE1细胞系中进一步验证。用siRNA干扰SiHa、Caski细胞(HPV-16阳性的宫颈癌细胞)中16E6/E7及HeLa细胞(HPV-18阳性的宫颈癌细胞)中18E6/E7的表达,通过Western blotting比较siRNA干扰前后E6和E7相关蛋白(E2F1、p53和Rab12)的表达差异。 结果 利用逆转录病毒包装系统成功构建稳定表达的细胞系,过表达E6/E7的细胞系中Rab12表达升高,干扰E6/E7的细胞系中Rab12的表达降低。 结论 HPV编码的早期癌蛋白E6/E7可调控Rab12的表达。
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