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Lookup NU author(s): Tomasz Zaremba, Huw ThomasORCiD, Mike Cole, Dr Sally Coulthard, Professor Ruth Plummer, Professor Nicola CurtinORCiD
There is a wide inter-individual variation in PARP activity, which may have implications for health. We investigated if the variation (i) is due to polymorphisms in the PARP-1 gene or PARP-1 protein expression and (ii) affects patients' response to anticancer treatment. We studied 56 healthy volunteers (HV) and 118 cancer patients (CP), with supporting in vivo experiments. PARP activity ranged between 10-2600 pmol PAR/106 cells and expression between 0.02-1.55 ng PARP-1/µg protein. PARP-1 expression correlated with activity in HV (R2=0.19, P=0.003) and CP (R2=0.06, P=0.01). A short CA repeat in the promoter was significantly associated with increased cancer risk (OR, 5.22; 95% CI, 1.79-15.24). PARP activity was higher in men than women (P=0.04) in the HV. Male mice also had higher PARP activity than females or castrated males. Estrogen supplementation activated PARP in PBMCs from female mice (P=0.003) but inhibited PARP in their livers by 80%. PARP activity and expression were not dependent on the investigated polymorphisms but there was a modest correlation of PARP activity with expression. Studies in the HV revealed sex differences in PARP activity, confirmed in mice and associated with sex hormones. Toxic response to treatment was not associated with PARP activity and/or expression.
Author(s): Zaremba T, Thomas HD, Cole M, Coulthard SA, Plummer ER, Curtin NJ
Publication type: Article
Publication status: Published
Journal: Biochemical Journal
Year: 2011
Volume: 436
Issue: 3
Pages: 671–679
Print publication date: 25/03/2011
Date deposited: 25/05/2012
ISSN (print): 0264-6021
ISSN (electronic): 1470-8728
Publisher: Portland Press Ltd.
URL: http://dx.doi.org/10.1042/BJ20101723
DOI: 10.1042/BJ20101723
PubMed id: 21434873
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