School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, PR China.
Oncol Rep. 2010 Dec;24(6):1599-604. doi: 10.3892/or_00001023.
The HPV-16 early proteins E6 and E7 are considered to function as oncoproteins in cervical cancer. DNA methyltransferase 1 (DNMT1) is one of the enzymes involved in epigenetic silencing of tumor suppressor genes. In the present study, the functional role and regulation of DNMT1 in HPV-16 E6 associated cervical cancer development were examined. Knockdown of E6 in HPV-16 positive human cervical carcinoma SiHa and CaSki cells led to the increase in p53, repression of DNMT1 protein and promoter activity. Moreover, p53 knockdown increased the DNMT1 protein as well as promoter activity, indicating that p53 may mediate E6 upregulation of DNMT1. In addition, E6 knockdown induced growth retardation in SiHa cells, and the effect was partially reverted by DNMT1 overexpression. The results suggest that HPV-16 E6 may act through p53/ DNMT1 to regulate the development of cervical cancer.
HPV-16 早期蛋白 E6 和 E7 被认为在宫颈癌中起癌蛋白作用。DNA 甲基转移酶 1(DNMT1)是参与肿瘤抑制基因表观遗传沉默的酶之一。在本研究中,研究了 DNMT1 在 HPV-16 E6 相关宫颈癌发展中的功能作用和调节作用。在 HPV-16 阳性的人宫颈癌细胞系 SiHa 和 CaSki 中敲低 E6 导致 p53 增加,DNMT1 蛋白和启动子活性受到抑制。此外,p53 敲低增加了 DNMT1 蛋白和启动子活性,表明 p53 可能介导 E6 对 DNMT1 的上调。此外,E6 敲低诱导 SiHa 细胞生长迟缓,DNMT1 过表达部分逆转了这种作用。结果表明,HPV-16 E6 可能通过 p53/DNMT1 作用来调节宫颈癌的发展。