Oncotarget

Research Papers:

Resistance to the nucleotide analogue cidofovir in HPV(+) cells: a multifactorial process involving UMP/CMP kinase 1

Dimitri Topalis _, Tatiane C. Nogueira, Tim De Schutter, Chahrazade El Amri, Marcela Krečmerová, Lieve Naesens, Jan Balzarini, Graciela Andrei and Robert Snoeck

PDF  |  HTML  |  Supplementary Files  |  How to cite  |  Order a Reprint

Oncotarget. 2016; 7:10386-10401. https://doi.org/10.18632/oncotarget.7006

Metrics: PDF 861 views  |   HTML 1015 views  |   ?  


Abstract

Dimitri Topalis1, Tatiane C. Nogueira1,*, Tim De Schutter1,*, Chahrazade El Amri2, Marcela Krečmerová3, Lieve Naesens1, Jan Balzarini1, Graciela Andrei1, Robert Snoeck1

1Rega Institute for Medical Research, KU Leuven, 3000 Leuven, Belgium

2Sorbonne Universités, UPMC University Paris 06, UMR 8256, B2A, Biological Adaptation and Ageing, Integrated Cellular Ageing and Inflammation, Molecular and Functional Enzymology, Paris, 75252 Paris Cedex 05, France

3Institute of Organic Chemistry and Biochemistry, Academy of Sciences of The Czech Republic, v.v.i., CZ-166 10 Prague 6, Czech Republic

*These authors have contributed equally to this work

Correspondence to:

Dimitri Topalis, e-mail: dimitrios.topalis@rega.kuleuven.be

Keywords: human papillomavirus, cervical carcinoma, UMP-CMP kinase, cidofovir, NTP metabolism

Received: July 09, 2015     Accepted: January 05, 2016     Published: January 25, 2016

ABSTRACT

Human papillomavirus (HPV) is responsible for cervical cancer, and its role in head and neck carcinoma has been reported. No drug is approved for the treatment of HPV-related diseases but cidofovir (CDV) exhibits selective antiproliferative activity.

In this study, we analyzed the effects of CDV-resistance (CDVR) in two HPV(+) (SiHaCDV and HeLaCDV) and one HPV(−) (HaCaTCDV) tumor cell lines. Quantification of CDV metabolites and analysis of the sensitivity profile to chemotherapeutics was performed. Transporters expression related to multidrug-resistance (MRP2, P-gp, BCRP) was also investigated.

Alterations of CDV metabolism in SiHaCDV and HeLaCDV, but not in HaCaTCDV, emerged via impairment of UMP/CMPK1 activity. Mutations (P64T and R134M) as well as down-regulation of UMP/CMPK1 expression were observed in SiHaCDV and HeLaCDV, respectively. Altered transporters expression in SiHaCDV and/or HeLaCDV, but not in HaCaTCDV, was also noted.

Taken together, these results indicate that CDVR in HPV(+) tumor cells is a multifactorial process.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 7006