Department of Biology, Clarkson University, Potsdam, NY 13699-5805, USA.
Virology. 2011 Dec 5;421(1):19-27. doi: 10.1016/j.virol.2011.09.014. Epub 2011 Oct 5.
The Human Papillomavirus type-16 (HPV-16) E6 and E7 oncogenes are selectively retained and expressed in cervical carcinomas, and expression of E6 and E7 is sufficient to immortalize human cervical epithelial cells. Expression of the epidermal growth factor receptor (EGFR) is often increased in cervical dysplasia and carcinoma, and HPV oncoproteins stimulate cell growth via the EGFR pathway. We found that erlotinib, a specific inhibitor of EGFR tyrosine kinase activity, prevented immortalization of cultured human cervical epithelial cells by the complete HPV-16 genome or the E6/E7 oncogenes. Erlotinib stimulated apoptosis in cells that expressed HPV-16 E6/E7 proteins and induced senescence in a subpopulation of cells that did not undergo apoptosis. Since immortalization by HPV E6/E7 is an important early event in cervical carcinogenesis, the EGFR is a potential target for chemoprevention or therapy in women who have a high risk for cervical cancer.
人乳头瘤病毒 16 型(HPV-16)E6 和 E7 癌基因在宫颈癌中被选择性保留和表达,并且 E6 和 E7 的表达足以使宫颈上皮细胞永生化。表皮生长因子受体(EGFR)的表达在宫颈发育不良和癌中常常增加,HPV 癌蛋白通过 EGFR 途径刺激细胞生长。我们发现,表皮生长因子受体酪氨酸激酶活性的特异性抑制剂厄洛替尼可防止完整的 HPV-16 基因组或 E6/E7 癌基因使培养的人宫颈上皮细胞永生化。厄洛替尼刺激表达 HPV-16 E6/E7 蛋白的细胞凋亡,并诱导未发生凋亡的细胞亚群衰老。由于 HPV E6/E7 的永生化是宫颈癌发生的重要早期事件,因此 EGFR 是高危女性宫颈癌化学预防或治疗的潜在靶点。