Branislav Rovcanin

Dr. Branislav Rovcanin

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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19 July 2016 in Current Medicinal Chemistry
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Journal Article
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BRBranislav Rovcanin
Branislav Rovcanin
BMBranislava Medic
Branislava Medic
Gordana KocicGordana Kocic
Gordana Kocic
TCTatjana Cebovic
Tatjana Cebovic
MRMarko Ristic
Marko Ristic
MPMilica Prostran
Milica Prostran
Ischemic reperfusion kidney injury (IRKI) is a complex pathophysiological event, which is the most common cause of the acute kidney injury. The key characteristic of IRKI is a reduction in glomerular filtration rate, which implies an underlying impairment in hemodynamic regulation. In recent decades, convincing evidence illuminated the molecular and pathological events in the acute kidney injury, revealing the role of ischemia/reperfusion, oxidative stress, apoptosis, inflammation, fibrosis and changes in gene expression which activate different signaling pathways. The cascade of inflammation events is a key mediator of IRKI, which includes the inflammation process, complement activation and mobilization of innate immunity. Oxidative stress represents the increased presence of various free radicals that cannot be buffered by the antioxidant capacity which comprises of enzymatic and non-enzymatic components. Renal tissue injury during ischemia/reperfusion comes as a result of membrane lipids peroxidation, oxidative damage of proteins and DNA and results in apoptosis and necrosis. It is evident from many studies that augmentation of the antioxidant defense mechanisms has a protective role on kidney tissue. In recent years, the importance of heat-shock proteins and MicroRNAs in the pathogenesis of IRKI has been revealed and there are promising indications that in future they could serve as diagnostic biomarkers or therapeutic targets. Striking changes in global gene expression were shown, providing a great potential for fundamental understanding and clinical management of IRKI. The clinical outcome among patients with kidney transplantation will have the furthermost advance from the better understanding of the underlying molecular pathology of IRKI.

25 May 2017 in BMC Cancer
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Journal Article
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BOBranisav Oluic
Branisav Oluic
IPIvan Paunovic
Ivan Paunovic
ZLZlatibor Loncar
Zlatibor Loncar
VDVladimir Djukic
Vladimir Djukic
ADAleksandar Diklic
Aleksandar Diklic
Vladan ZivaljevicVladan Zivaljevic
Vladan Zivaljevic
Hurthle cell carcinoma makes up 3 to 5% of all thyroid cancers and is considered to be a true rarity. The aim of our study was to analyze clinical characteristics and survival rates of patients with Hurthle cell carcinoma. Clinical data regarding basic demographic characteristics, tumor grade, type of surgical treatment and vital status were collected. Methods of descriptive statistics and Kaplan-Meier survival curves were used for statistical analysis. Cox proportional hazards regression was used to identify independent predictors. During the period from 1995 to 2014, 239 patients with Hurthle cell carcinoma were treated at our Institution. The average age of the patients was 54.3, with female to male ratio of 3.6:1 and average tumor size was 41.8 mm. The overall recurrence rate was 12.1%, with average time for relapse of 90.74 months and average time without any signs of the disease of 222.4 months. Overall 5-year, 10-year and 20-year survival rates were 89.4%, 77.2%, 61.9% respectively. The 5-year, 10-year and 20-year cancer specific survival rates were 94.6%, 92.5%, 87.4%, respectively. When disease free interval was observed, 5-year, 10-year and 20-year rates were 91.1%, 86.2%, 68.5%, respectively. The affection of both thyroid lobes and the need for reoperation due to local relapse were unfavorable independent prognostic factors, while total thyroidectomy as primary procedure was favorable predictive factor for cancer specific survival. Hurthle cell carcinoma is a rare tumor with an encouraging prognosis and after adequate surgical treatment recurrences are rare.

30 November 2012 in Cell Biochemistry and Biophysics
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Journal Article
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SRSandra Radenkovic
Sandra Radenkovic
ZMZorica Milosevic
Zorica Milosevic
GKGordana Konjevic
Gordana Konjevic
KKKatarina Karadzic
Katarina Karadzic
BRBranislav Rovcanin
Branislav Rovcanin
VJVladimir Jurisic
Vladimir Jurisic

30 November 2015 in BioMed Research International
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Journal Article
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BMBranislava Medić
Branislava Medić
BRBranislav Rovcanin
Branislav Rovcanin
GJGordana Basta Jovanović
Gordana Basta Jovanović
SRSanja Radojević-Škodrić
Sanja Radojević-Škodrić
MPMilica Prostran
Milica Prostran
Despite the recent findings concerning pathogenesis and novel therapeutic strategies, cardiovascular disease (CVD) still stays the leading cause of morbidity and mortality in patients with renal dysfunction, especially acute kidney injury (AKI). Early detection of patients with impaired renal function with cardiovascular risk may help ensure more aggressive treatment and improve clinical outcome. Kidney injury molecule-1 (KIM-1) is a new, promising marker of kidney damage which is currently the focus of countless studies worldwide. Some recent animal and human studies established KIM-1 as an important marker of acute tubular necrosis (ATN) and reliable predictor of development and prognosis of AKI. Food and Drug Administration (FDA) in USA acclaimed KIM-1 as an AKI biomarker for preclinical drug development. Recent data suggest the importance of monitoring of KIM-1 for early diagnosis and clinical course not only in patients with various forms of AKI and other renal diseases but also in patients with cardiorenal syndrome, heart failure, cardiopulmonary bypass, cardiothoracic surgical interventions in the pediatric emergency setting, and so forth. The aim of this review article is to summarize the literature data concerning KIM-1 as a potential novel marker in the early diagnosis and prediction of clinical outcome of certain cardiovascular diseases.

19 July 2016 in Current Medicinal Chemistry
Verified
Journal Article
Closed access
BMBranislava Medi
Branislava Medi
BRBranislav Rovcanin
Branislav Rovcanin
KVKatarina Savic Vujovic
Katarina Savic Vujovic
DODanilo Obradovic
Danilo Obradovic
DDDusan Duric
Dusan Duric
Despite the recent findings concerning pathogenesis and novel therapeutic strategies, the mortality rate in patients with acute kidney injury (AKI) remains very high. Early detection of patients with impaired renal function may help to ensure more aggresive treatment and to improve clinical outcome. Serum creatinine is still gold standard of kidney injury, although it is well known as an insensitive and unreliable biomarker (for example, its concentration does not increase significantly until about half of the kidney function is lost). Considering these data, researches and clinicians are making great efforts in the past decade in order to discover and validate novel AKI biomarkers. Kidney injury molecule-1 (KIM-1), Neutrophil gelatinase-associated lipocalin (NGAL), Interleukin-18 (IL-18), Cystatin C (Cys-C) are some of new, promising markers of kidney damage which are currently in the focus of preclinical and clinical studies. Recent data suggest that some of these new biomarkers represent important parametars of acute tubular necrosis (ATN) and reliable predictors of development and prognosis of AKI. Beside that, monitoring of these markers could have significant importance for early diagnosis and clinical course, not only in patients with various forms of AKI and other renal diseases, but also in patients with cardiorenal syndrome, heart failure, cardiopulmonary bypass, cardiothoracical surgical interventions, in the pediatric emergency setting etc. Aim of this review is to summarize the literature data concerning some new biomarkers, to evaluate their role as well as their limitations in the early diagnosis and prediction of clinical outcome of some renal diseases.

27 April 2013 in Digestive Diseases and Sciences
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KGKristina Gopcevic
Kristina Gopcevic
KRKristina R.
Kristina R.
BRBranislav Rovcanin
Branislav Rovcanin
BRBranislav R.
Branislav R.
STSvetislav B. Tatić
Svetislav B. Tatić
VDVesna V. Dragutinović
Vesna V. Dragutinović