Kate Whittington
University of Bristol
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Publication
Featured researches published by Kate Whittington.
International Review of Cytology-a Survey of Cell Biology | 2007
Helen D. Nicholson; Kate Whittington
Oxytocin is a peptide hormone produced by the neurohypophysis. The discovery that the peptide is produced locally within the male and female reproductive tracts has raised the possibility that oxytocin may have paracrine and autocrine actions outside of the nervous system. Oxytocin and its receptor have been identified in the human prostate. The prostate is an androgen-dependent organ whose function is to secrete components of the seminal fluid. Oxytocin has been shown to modulate contractility of prostate tissue and also to regulate local concentrations of the biologically active androgens. Oxytocin has also been shown to regulate cell growth. Prostate disease is common and results from abnormal growth of the gland. Oxytocin concentrations are altered in both benign and malignant prostate diseases and in vitro studies suggest that the peptide may be involved in the pathophysiology of these diseases.
BMC Research Notes | 2009
Rebecca Wiggins; Patrick J Horner; Kate Whittington; Christopher H Holmes
BackgroundEpithelial cells in first catch urine (FCU) specimens from 87 men with and without urethritis were quantified. Epithelial cells were broadly categorised into transitional and squamous populations using morphological characteristics and immunostaining with anti-pan leukocyte and anti-cytokeratin monoclonal antibodies.FindingsThe majority (77/87 = 89%) of samples contained both transitional (76/87 = 87%; range 1 × 104 – 6 × 105, median 6 × 104) and squamous (57/87 = 66%; range 1 × 104 – 8 × 105, median 2 × 104) epithelial cells. The number of transitional cells correlated with the number of squamous cells (Spearmans rho = 0.697 p < 0.001). Squamous, but not transitional, cell numbers correlated with leukocyte numbers (Spearmans rho = 0.216 p = 0.045 and rho = 0.171 and p = 0.113, respectively). However there was no significant difference in epithelial cell numbers between men with and without urethritis. Nevertheless, some men with urethritis had relatively high numbers of transitional cells in their FCU. Transitional cells were morphologically heterogeneous and appeared to display complex cytokeratin phenotypes.ConclusionFurther studies are required to explore the complexity of epithelial cell populations in urine. These would provide novel opportunities for studying cellular interactions of C. trachomatis in male urethral infections, about which little is currently known.
BMC Urology | 2008
Hp Burden; Cr Davis; Sophie Tate; Raj Persad; Ch Holmes; Kate Whittington
BackgroundWorldwide, the use of prostate specific antigen (PSA) testing as a screen for prostate cancer is contentious. Whilst there is no National UK Screening programme, many men undergo opportunistic screening. This study investigates UK urologists usage of PSA and the awareness surrounding the Department of Health (DoH) PSA guidelines.MethodsUrologists were sent a questionnaire regarding PSA cut-off values.ResultsOf the 733 urologists eligible to participate in this study 346 returned completed questionnaires giving a response rate of 47%. The most commonly generally used age-related PSA cut-off values (36% of respondents) are – 3.5 ng/ml for 50 – 59 year olds, 4.5 ng/ml for 60 – 69 year olds and 6.5 ng/ml for over 70 year olds. Two-thirds (58%, 200/346) of respondents were aware of the DoH PSA guidelines but only 20% (n = 69/346) follow these guidelines. The majority of respondents (68%, n = 234/346) used higher PSA cut-offs than recommended by the DoH. The level of compliance showed marked regional variation with a range from 7% to 44% (median 19%). In addition, it was apparent that lower PSA cut-off values were used in private practice as opposed to the National Health Service.ConclusionA nationwide lack of agreement on PSA cut-off values may generate a variable standard of care both regionally and in NHS versus private practice. Generally, higher PSA cut-off values are being used than recommended by the DoH guidance.
Human Reproduction Update | 2006
Hemlata Thackare; Helen D. Nicholson; Kate Whittington
International Journal of Andrology | 1999
Kate Whittington; Shona C. Harrison; Katherine M. Williams; Joanne L. Day; Eileen A. McLaughlin; M.G.R. Hull; W. Christopher L. Ford
Reproduction | 2001
Kate Whittington; Steve Assinder; T. Parkinson; Kr Lapwood; Helen D. Nicholson
Cell and Tissue Research | 2004
Kate Whittington; Steve Assinder; Maree Gould; Helen D. Nicholson
The Prostate | 2007
Kate Whittington; Belinda Connors; Keith J. King; Steve Assinder; Karole Hogarth; Helen D. Nicholson
Human Reproduction | 2004
Kate Whittington; Julian Cook; Christopher L.R. Barratt; Julian M. Jenkins
Archive | 2009
Rachael Knight; Kate Whittington; W. Chris L. Ford; Julian Jenkins