Format

Send to

Choose Destination

See 1 citation found by title matching your search:

Oncotarget. 2016 Jun 21;7(25):37608-37621. doi: 10.18632/oncotarget.8058.

Immortalization capacity of HPV types is inversely related to chromosomal instability.

Author information

1
Department of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
2
Department of Molecular Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
3
Genome Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
4
Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
5
DDL Diagnostic Laboratory, Voorburg, The Netherlands.

Abstract

High-risk human papillomavirus (hrHPV) types induce immortalization of primary human epithelial cells. Previously we demonstrated that immortalization of human foreskin keratinocytes (HFKs) is HPV type dependent, as reflected by the presence or absence of a crisis period before reaching immortality. This study determined how the immortalization capacity of ten hrHPV types relates to DNA damage induction and overall genomic instability in HFKs.Twenty five cell cultures obtained by transduction of ten hrHPV types (i.e. HPV16/18/31/33/35/45/51/59/66/70 E6E7) in two or three HFK donors each were studied.All hrHPV-transduced HFKs showed an increased number of double strand DNA breaks compared to controls, without exhibiting significant differences between types. However, immortal descendants of HPV-transduced HFKs that underwent a prior crisis period (HPV45/51/59/66/70-transduced HFKs) showed significantly more chromosomal aberrations compared to those without crisis (HPV16/18/31/33/35-transduced HFKs). Notably, the hTERT locus at 5p was exclusively gained in cells with a history of crisis and coincided with increased expression. Chromothripsis was detected in one cell line in which multiple rearrangements within chromosome 8 resulted in a gain of MYC.Together we demonstrated that upon HPV-induced immortalization, the number of chromosomal aberrations is inversely related to the viral immortalization capacity. We propose that hrHPV types with reduced immortalization capacity in vitro, reflected by a crisis period, require more genetic host cell aberrations to facilitate immortalization than types that can immortalize without crisis. This may in part explain the observed differences in HPV-type prevalence in cervical cancers and emphasizes that changes in the host cell genome contribute to HPV-induced carcinogenesis.

KEYWORDS:

E6/E7; arrayCGH; chromothripsis; high-risk HPV; transformation

PMID:
26993771
PMCID:
PMC5122336
DOI:
10.18632/oncotarget.8058
[Indexed for MEDLINE]
Free PMC Article

Conflict of interest statement

RDMS, CJLMM and PJFS have minority stake in Self-Screen B.V., a spin-off company of VU University Medical Center Amsterdam. CJLMM has participated in the sponsored speaker's bureau of Merck, GSK, Qiagen, Menarini, Seegene, and Roche, and served occasionally on the scientific advisory board of GSK, Qiagen, Merck, and Roche. CJLMM has occasionally been consultant for Qiagen and Genticel and is a minority shareholder of Diassay B.V. Formerly CJLMM was a minority shareholder of Delphi Biosciences. PJFS has been on the speaker's bureau of Roche, Abbott, Gen-Probe, Qiagen and Seegene. He is consultant for Crucell Holland B.V. WGVQ is a minority shareholder of Diassay B.V. and has obtained grants from GlaxoSmithKline. All other authors declare that they have no conflicts of interest.

Supplemental Content

Full text links

Icon for Impact Journals, LLC Icon for PubMed Central
Loading ...
Support Center