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A simple method for detecting oncofetal chondroitin sulfate glycosaminoglycans in bladder cancer urine

Clausen, Thomas Mandel (author)
University of British Columbia (UBC),Köpenhamns universitet,University of Copenhagen
Kumar, Gunjan (author)
University of British Columbia (UBC)
Ibsen, Emilie K. (author)
Köpenhamns universitet,University of Copenhagen
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Ørum-Madsen, Maj S. (author)
University of British Columbia (UBC)
Hurtado-Coll, Antonio (author)
University of British Columbia (UBC)
Gustavsson, Tobias (author)
Köpenhamns universitet,University of Copenhagen
Agerbæk, Mette (author)
Köpenhamns universitet,University of Copenhagen
Gatto, Francesco, 1987 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Todenhöfer, Tilman (author)
Eberhard Karls Universität Tübingen,Eberhard Karls University of Tübingen
Basso, U. (author)
Knowles, Margaret A. (author)
St James's University Hospital
Sanchez-Carbayo, Marta (author)
Universidad Pontificia de Salamanca,Pontifical University of Salamanca
Salanti, Ali (author)
Köpenhamns universitet,University of Copenhagen
Black, Peter C. (author)
University of British Columbia (UBC)
Daugaard, Mads (author)
University of British Columbia (UBC)
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 (creator_code:org_t)
2020-07-27
2020
English.
In: Cell Death Discovery. - : Springer Science and Business Media LLC. - 2058-7716. ; 6:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Proteoglycans in bladder tumors are modified with a distinct oncofetal chondroitin sulfate (ofCS) glycosaminoglycan that is normally restricted to placental trophoblast cells. This ofCS-modification can be detected in bladder tumors by the malarial VAR2CSA protein, which in malaria pathogenesis mediates adherence of parasite-infected erythrocytes within the placenta. In bladder cancer, proteoglycans are constantly shed into the urine, and therefore have the potential to be used for detection of disease. In this study we investigated whether recombinant VAR2CSA (rVAR2) protein could be used to detect ofCS-modified proteoglycans (ofCSPGs) in the urine of bladder cancer patients as an indication of disease presence. We show that ofCSPGs in bladder cancer urine can be immobilized on cationic nitrocellulose membranes and subsequently probed for ofCS content by rVAR2 protein in a custom-made dot-blot assay. Patients with high-grade bladder tumors displayed a marked increase in urinary ofCSPGs as compared to healthy individuals. Urine ofCSPGs decreased significantly after complete tumor resection compared to matched urine collected preoperatively from patients with bladder cancer. Moreover, ofCSPGs in urine correlated with tumor size of bladder cancer patients. These findings demonstrate that rVAR2 can be utilized in a simple biochemical assay to detect cancer-specific ofCS-modifications in the urine of bladder cancer patients, which may be further developed as a noninvasive approach to detect and monitor the disease.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Klinisk laboratoriemedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Clinical Laboratory Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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