Nina Fokter Dovnik

Dr. Nina Fokter Dovnik


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 May 2009 in BMC Clinical Pharmacology
Verified
Journal Article
Open access
PDF file
MBMiran Brvar
Miran Brvar
NDNina Fokter Dovnik
Nina Fokter Dovnik
Matjaz BuncMatjaz Bunc
Matjaz Bunc
MMMartin Mozina
Martin Mozina
Adverse Drug Reactions (ADRs) have been regarded as a major public health problem since they represent a sizable percentage of admissions. Unfortunately, there is a wide variation of ADR related admissions among different studies. The aim of this study was to evaluate the frequency of ADR related admissions and its dependency on reporting and method of detection, urgency of admissions and included medical departments reflecting department/hospital type within one study.

1 February 2010 in Wiener klinische Wochenschrift
Verified
Journal Article
Closed access
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NDNina Fokter Dovnik
Nina Fokter Dovnik
MMMartin Možina
Martin Možina
MBMiran Brvar
Miran Brvar

1 February 2020 in Cells
Verified
Journal Article
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Andraž DovnikAndraž Dovnik
Andraž Dovnik
NDNina Fokter Dovnik
Nina Fokter Dovnik
Vitamin D is a lipid soluble vitamin involved primarily in calcium metabolism. Epidemiologic evidence indicates that lower circulating vitamin D levels are associated with a higher risk of ovarian cancer and that vitamin D supplementation is associated with decreased cancer mortality. A vast amount of research exists on the possible molecular mechanisms through which vitamin D affects cancer cell proliferation, cancer progression, angiogenesis, and inflammation. We conducted a systematic review of the literature on the effects of vitamin D on ovarian cancer cell.

27 November 2015 in Radiology and Oncology
Verified
Journal Article
Open access
MLMaja Lampelj
Maja Lampelj
DADarja Arko
Darja Arko
NCNina Cas-Sikosek
Nina Cas-Sikosek
RKRajko Kavalar
Rajko Kavalar
MRMaja Ravnik
Maja Ravnik
ITIztok Takac
Iztok Takac
Background. Urokinase plasminogen activator (uPA) and plasminogen activator inhibitor type-1 (PAI-1) play a key role in tumour invasion and metastasis. High levels of both proteolytic enzymes are associated with poor prognosis in breast cancer patients. The purpose of this study was to evaluate the correlation between traditional prognostic factors and uPA and PAI-1 expression in primary tumour of breast cancer patients. Patients and methods. 606 primary breast cancer patients were enrolled in the prospective study in the Department of gynaecological oncology and breast oncology at the University Medical Centre Maribor between the years 2004 and 2010. We evaluated the traditional prognostic factors (age, menopausal status, tumour size, pathohistological type, histologic grade, lymph node status, lymphovascular invasion and hormone receptor status), together with uPA and PAI-1. We used Spearman’s rank correlation, Mann Whitney U test and χ 2 test for statistical analysis. Results. Our findings indicate a positive correlation between uPA and tumour size (p < 0.001), grade (p < 0.001), histological type (p < 0.001), lymphovascular invasion (p = 0.01) and a negative correlation between uPA and hormone receptor status (p < 0.001). They also indicate a positive correlation between PAI-1 and tumour size (p = 0.004), grade (p < 0.001), pathohistological type (p < 0.001) and negative correlation between PAI-1 and hormone receptor status (p = 0.002). Conclusions. Our study showed a relationship between uPA and PAI-1 and traditional prognostic factors. Their role as prognostic and predictive factors remains to be further evaluated.

1 August 2012 in Wiener klinische Wochenschrift
Verified
Journal Article
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Iztok TakačIztok Takač
Iztok Takač
RKRajko Kavalar
Rajko Kavalar
DADarja Arko
Darja Arko
NDNina Fokter Dovnik
Nina Fokter Dovnik

7 February 2016 in Radiology and Oncology
Verified
Journal Article
Open access
PDF file
NDNina Fokter Dovnik
Nina Fokter Dovnik
ITIztok Takac
Iztok Takac
Background: The association of HER2 status with urokinase plasminogen activator (uPA) and plasminogen activator inhibitor 1 (PAI-1) levels raises the question whether uPA/PAI-1 level carries additional clinically relevant prognostic information independently from HER2 status. The aim of our study was to compare the prognostic value of uPA/PAI-1 level, HER2 status, and traditional prognostic factors for survival in node-negative breast cancer patients. Patients and methods: A retrospective analysis of 858 node-negative breast cancer patients treated in Maribor University Clinical Center, Slovenia, in the years 2000–2009 was performed. Data were obtained from patient medical records. The median follow-up time was 100 months. Univariate and multivariate analyses of disease-free (DFS) and overall survival (OS) were performed using the Cox regression and the Cox proportional hazards model. Results: In univariate analysis, age, tumor size, grade, lymphovascular invasion, HER2 status and UPA/PAI-1 level were associated with DFS, and age, tumor size, grade, and uPA/PAI-1 level were associated with OS. In the multivariate model, the most important determinants of DFS were age, estrogen receptor status and uPA/PAI-1 level, and the most important factors for OS were patient age and tumor grade. The HR for death from any cause in the multivariate model was 1.98 (95% CI 0.83–4.76) for patients with high uPA and/or PAI-1 compared to patients with both values low. Conclusions: uPA/PAI-1 level clearly carries an independent prognostic value regardless of HER2 status in node-negative breast cancer and could be used in addition to HER2 and other markers to guide clinical decisions in this setting.