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      SCUBE1: a promising biomarker in renal cell cancer

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          ABSTRACT

          Purpose

          To investigate the efficacy of signal peptide-CUB-EGF domain-containing protein 1 (SCUBE-1) as a novel biomarker of renal tumors.

          Materials and Methods

          48 individuals were included in the study. The patient group (Group-1) consisted of 23 subjects diagnosed with renal tumor, and the control group (Group-2) of 25 healthy individuals. Patients diagnosed with renal tumor received surgical treatment consisting of radical or partial nephrectomy. Blood specimens were collected following overnight fasting. Signal peptide-CUB-EGF domain-containing protein 1 (SCUBE-1), soluble urokinase plasminogen activator receptor (suPAR) and carbonic anhydrase IX (CA IX) levels were measured from plasma samples. Patients in groups 1 and 2 were compared in terms of these biochemical parameters.

          Results

          The 23-member renal tumor group was made up of 17 (73.91%) male and 6 (26.08%) female patients with a mean age of 58.5±15.7 years (range 25 to 80). The 24-member healthy control group was made up of 16 (64%) male and 9 (36%) female subjects with a mean age of 52.4±9.12 years (range 40 to 67). Analysis revealed significant elevation in SCUBE-1 levels in the renal tumor group (p=0.005). No significant differences were detected between the groups with regard to CA IX or suPAR measurements (p=0.062 vs. p=0.176).

          Conclusions

          SCUBE-1 appears to represent a promising biomarker in the diagnosis and follow-up of patients with renal tumor.

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          Most cited references31

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          The plasminogen activation system in tumor growth, invasion, and metastasis.

          Generation of the serine proteinase plasmin from the extracellular zymogen plasminogen can be catalyzed by either of two other serine proteinases, the urokinase- and tissue-type plasminogen activators (uPA and tPA). The plasminogen activation system also includes the serpins PAI-1 and PAI-2, and the uPA receptor (uPAR). Many findings, gathered over several decades, strongly suggest an important and causal role for uPA-catalyzed plasmin generation in cancer cell invasion through the extracellular matrix. Recent evidence suggests that the uPA system is also involved in cancer cell-directed tissue remodeling. Moreover, the system also supports cell migration and invasion by plasmin-independent mechanisms, including multiple interactions between uPA, uPAR, PAI-1, extracellular matrix proteins, integrins, endocytosis receptors, and growth factors. These interactions seem to allow temporal and spatial reorganizations of the system during cell migration and a selective degradation of extracellular matrix proteins during invasion. The increased knowledge about the plasminogen activation system may allow utilization of its components as targets for anti-invasive therapy.
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            Cancer statistics, 1999.

            The Surveillance Research Program of the American Cancer Society's Department of Epidemiology and Surveillance Research reports its 33rd annual compilation of cancer frequency, incidence, mortality, and survival data for the United States.
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              suPAR: The Molecular Crystal Ball

              soluble urokinase Plasminogen Activator Receptor (suPAR) levels reflect inflammation and elevated suPAR levels are found in several infectious diseases and cancer. suPAR exists in three forms; suPARI-III, suPARII-III and suPARI which show different properties due to structural differences. Studies suggest that full-length suPAR is a regulator of uPAR/uPA by acting as uPA-scavenger, whereas the cleaved suPARII-III act as a chemotactic agent promoting the immune response via the SRSRY sequence in the linker-region. This review focus on the various suPAR fragments and their involvement in inflammation and pathogenic processes. We focus on the molecular mechanisms of the suPAR fragments and the link to the inflammatory process, as this could lead to medical applications in infectious and pathological conditions.
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                Author and article information

                Journal
                Int Braz J Urol
                Int Braz J Urol
                ibju
                International Brazilian Journal of Urology : official journal of the Brazilian Society of Urology
                Sociedade Brasileira de Urologia
                1677-5538
                1677-6119
                Jul-Aug 2017
                Jul-Aug 2017
                : 43
                : 4
                : 638-643
                Affiliations
                [1 ]Department of Urology, Karadeniz Technical University, Faculty of Medicine, Trabzon, Turkey;
                [2 ] Program of Medical Laboratory Techniques, Karadeniz Technical University, Vocational School of Health Sciences, Trabzon, Turkey;
                [3 ]Department of Nutrition and Dietetics, Karadeniz Technical University, Faculty of Health Sciences, Trabzon, Turkey;
                [4 ]Department of Medical Biochemistry, Karadeniz Technical University, Faculty of Medicine, Trabzon, Turkey;
                [5 ]Department of Chemistry and Chemical Processing Technology, Ordu University, Ulubey Vocational School, Ordu, Turkey
                Author notes
                Correspondence address: Ersagun Karagüzel, MD. Department of Urology. Karadeniz Technical University, School of Medicine. 61080, Trabzon, Turkey. Fax: + 90 462 325-0518. E-mail: ersagunkaraguzel@ 123456gmail.com

                CONFLICT OF INTEREST

                None declared.

                Article
                S1677-5538.IBJU.2016.0316
                10.1590/S1677-5538.IBJU.2016.0316
                5557438
                28379666
                d1007e9b-60d8-4a9f-9d69-94532ad1eb12

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 June 2016
                : 04 January 2017
                : 22 March 2017
                Page count
                Figures: 0, Tables: 3, Equations: 0, References: 28, Pages: 6
                Categories
                Original Article

                carcinoma, renal cell,biomarkers
                carcinoma, renal cell, biomarkers

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