HPV-18 transformed cells fail to arrest in G1 in response to quercetin treatment

• Published in: Virus research 2005-05, Vol.109 (2), p.203-209
• Main Authors: Beniston, R.G., Campo, M.S.
• Format: Article
• Language: English
• Subjects: Bovine papillomavirus; Cell Cycle Proteins - analysis; Cell Transformation, Viral; Cells, Cultured; Cyclin-Dependent Kinase Inhibitor p27; G1 Phase - drug effects; Gene Expression Regulation, Viral - drug effects; Growth Inhibitors - pharmacology; HPV; Human papillomavirus; Human papillomavirus 16; Humans; Keratinocytes - virology; LCR; p27 Kip1; Papillomaviridae - physiology; Pteridium aquilinum; Quercetin; Quercetin - pharmacology; Tumor Suppressor Proteins - analysis
• ISSN: 0168-1702; 1872-7492
• DOI: 10.1016/j.virusres.2004.12.002

Previous work with primary human keratinocytes demonstrated that quercetin, a potent mutagen found in high levels in bracken fern ( Pteridium aquilinum), arrested cells in G1 with concomitant elevation of the cyclin-dependent kinase inhibitor (cdki) p27 Kip1. Expression of the human papillomavirus type 16 (HPV-16) E6 and E7 oncoproteins, under transcriptional control of a heterologous promoter, in transformed keratinocytes failed to abrogate this arrest [Beniston, R., Campo, M.S., 2003. Quercetin elevates p27(Kip1) and arrests both primary and HPV-16 E6/E7 transformed human keratinocytes in G1. Oncogene 22, 5504–5514]. Given the link between papillomavirus infection, bracken fern in the diet and cancer of the oesophagus in humans, we wished to investigate further whether cells transformed by the whole genome of HPV-16 or HPV-18, with E6 and E7 under the transcriptional control of their respective homologous promoters, would be similarly arrested in G1 by quercetin. In agreement with earlier work, quercetin arrested HPV-16 transformed cells in G1 with an increase in the cyclin-dependent kinase inhibitor p27 Kip1. However, HPV-18 transformed cells did not arrest after quercetin treatment. The failure of HPV-18 transformed cells to arrest in G1 was linked to the up-regulation of the HPV-18 long control region (LCR) by quercetin, maintaining high expression of the viral transforming proteins. Transcriptional up-regulation of the HPV-18 LCR was mediated by a “quercetin responsive element” homologous to the one identified previously in the bovine papillomavirus type 4 (BPV-4) LCR.