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      Predictive Markers for Malignant Urothelial Transformation in Balkan Endemic Nephropathy: A Case–Control Study

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          Abstract

          Simple Summary

          Balkan endemic nephropathy (BEN) is chronic kidney disease caused by intoxication with Aristolochia plant. Apart from subtle decline of renal function that eventually results in kidney failure, the patients are at increased risk for urothelial carcinoma (UC) development. Based on the observed UC markers, the aim of this study was to examine urinary and plasma levels of some these markers in BEN patients without carcinoma, in order to potentially identify those with predictive value. Our study revealed either plasma or urinary survivin levels as a potential predictors of future malignant transformation of urothelium.

          Abstract

          Balkan endemic nephropathy (BEN) is a chronic tubulointerstitial disease frequently accompanied by urothelial carcinoma (UC). In light of the increased UC incidence and the markers observed in BEN patients with developed UC, the aim of the current case–control study is to assess survivin, p53 protein, growth factors and receptors (VEGF, VEGFR1, IGF I, IGF-1R and IGFBP5), tumor marker (TF)/CD142, circulating soluble Fas receptor and neopterin, as potentially predictive markers for UC in patients with BEN (52 patients), compared to healthy, age-matched subjects (40). A threefold increase was registered in both circulating and urinary survivin level in BEN patients. Especially noticeable was the ratio of U survivin/U Cr level five times the ratio of BEN patients associated with standard renal markers in multivariate regression models. The concentrations of VEGF, VEGFR1, (TF)/CD142, (sFas) were not significantly different in BEN patients, while urinary/plasma level demonstrated a significant decrease for VEGF. The levels of IGF I, IGFBP5 and IGF-1R were significantly reduced in the urine of BEN patients. Plasma concentration of neopterin was significantly higher, while urinary neopterin value was significantly lower in BEN patients compared to healthy controls, which reflected a significantly lower urine/plasma ratio and low local predictive value. As BEN is a slow-progressing chronic kidney disease, early detection of survivin may be proposed as potential predictor for malignant alteration and screening tool in BEN patients without the diagnosis of UC.

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          VEGFR1-positive haematopoietic bone marrow progenitors initiate the pre-metastatic niche.

          The cellular and molecular mechanisms by which a tumour cell undergoes metastasis to a predetermined location are largely unknown. Here we demonstrate that bone marrow-derived haematopoietic progenitor cells that express vascular endothelial growth factor receptor 1 (VEGFR1; also known as Flt1) home to tumour-specific pre-metastatic sites and form cellular clusters before the arrival of tumour cells. Preventing VEGFR1 function using antibodies or by the removal of VEGFR1(+) cells from the bone marrow of wild-type mice abrogates the formation of these pre-metastatic clusters and prevents tumour metastasis, whereas reconstitution with selected Id3 (inhibitor of differentiation 3)-competent VEGFR1+ cells establishes cluster formation and tumour metastasis in Id3 knockout mice. We also show that VEGFR1+ cells express VLA-4 (also known as integrin alpha4beta1), and that tumour-specific growth factors upregulate fibronectin--a VLA-4 ligand--in resident fibroblasts, providing a permissive niche for incoming tumour cells. Conditioned media obtained from distinct tumour types with unique patterns of metastatic spread redirected fibronectin expression and cluster formation, thereby transforming the metastatic profile. These findings demonstrate a requirement for VEGFR1+ haematopoietic progenitors in the regulation of metastasis, and suggest that expression patterns of fibronectin and VEGFR1+VLA-4+ clusters dictate organ-specific tumour spread.
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            Insulin-like growth factors and neoplasia.

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              Plasma insulin-like growth factor-I and prostate cancer risk: a prospective study.

              Insulin-like growth factor-I (IGF-I) is a mitogen for prostate epithelial cells. To investigate associations between plasma IGF levels and prostate cancer risk, a nested case-control study within the Physicians' Health Study was conducted on prospectively collected plasma from 152 cases and 152 controls. A strong positive association was observed between IGF-I levels and prostate cancer risk. Men in the highest quartile of IGF-I levels had a relative risk of 4.3 (95 percent confidence interval 1.8 to 10.6) compared with men in the lowest quartile. This association was independent of baseline prostate-specific antigen levels. Identification of plasma IGF-I as a predictor of prostate cancer risk may have implications for risk reduction and treatment.
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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                13 October 2020
                October 2020
                : 12
                : 10
                : 2945
                Affiliations
                [1 ]Department of Biochemistry, Faculty of Medicine, University of Niš, 18000 Niš, Serbia; andrej.veljkovic@ 123456medfak.ni.ac.rs
                [2 ]Serbian Academy of Sciences and Arts, 11000 Belgrade, Serbia; jovan.hadzi-djokic@ 123456sanu.ac.rs
                [3 ]Department of Anatomy, Faculty of Medicine, University of Niš, 18000 Niš, Serbia; jovana.cukuranovic.kokoris@ 123456medfak.ni.ac.rs (J.C.-K.); rade.cukuranovic@ 123456medfak.ni.ac.rs (R.C.); ivan.jovanovic@ 123456medfak.ni.ac.rs (I.J.)
                [4 ]Department of Pharmacy, Faculty of Medicine, University of Niš, 18000 Niš, Serbia; mihajlo.gajic@ 123456medfak.ni.ac.rs
                [5 ]Clinic of Nephrology, Clinical Center Niš, 18000 Niš, Serbia
                [6 ]Department of Surgery and Anesthesiology and Reanimatology, Faculty of Medicine, University of Niš, 18000 Niš, Serbia; dragoslav.basic@ 123456medfak.ni.ac.rs
                [7 ]Clinic of Urology, Clinical Center Niš, 18000 Niš, Serbia
                [8 ]Department of Chemistry, Faculty of Medicine, University of Niš, 18000 Serbia; andrija.smelcerovic@ 123456medfak.ni.ac.rs
                Author notes
                [* ]Correspondence: gordana.kocic@ 123456medfak.ni.ac.rs ; Tel.: +381-63-8122522; Fax: +381-18-510901
                Author information
                https://orcid.org/0000-0003-2386-2466
                Article
                cancers-12-02945
                10.3390/cancers12102945
                7599787
                33065960
                2f1a38bf-6c1e-4e20-89ed-0b8d545c2dea
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 11 August 2020
                : 25 September 2020
                Categories
                Article

                balkan endemic nephropathy (ben),aristolochic acid nephropathy,upper urothelial cancer,proteomic tumor markers,survivin

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