Studies of cellular retinol-binding protein (CRBP) in squamous-cell carcinomas of the head and neck region
Corresponding Author
G. Fex
Department of Clinical Chemistry, Malmö General Hospital, Sweden
Dept. of Clinical Chemistry, University of Lund, Malmö General Hospital, S-214 01 Malmö, SwedenSearch for more papers by this authorP. Wahlberg
Oto-Rhino-Laryngology, University Hospital of Lund, Sweden
Search for more papers by this authorA. Biörklund
Oto-Rhino-Laryngology, University Hospital of Lund, Sweden
Search for more papers by this authorJ. Wennerberg
Oto-Rhino-Laryngology, University Hospital of Lund, Sweden
Search for more papers by this authorCorresponding Author
G. Fex
Department of Clinical Chemistry, Malmö General Hospital, Sweden
Dept. of Clinical Chemistry, University of Lund, Malmö General Hospital, S-214 01 Malmö, SwedenSearch for more papers by this authorP. Wahlberg
Oto-Rhino-Laryngology, University Hospital of Lund, Sweden
Search for more papers by this authorA. Biörklund
Oto-Rhino-Laryngology, University Hospital of Lund, Sweden
Search for more papers by this authorJ. Wennerberg
Oto-Rhino-Laryngology, University Hospital of Lund, Sweden
Search for more papers by this authorAbstract
Cellular retinol-binding protein (CRBP) concentration was determined by radioimmunoassay in biopsies from normal mucosa and squamous-cell cancers of the head and neck region in 26 patients. The plasma concentrations of retinol, retinol-binding protein (RBP), prealbumin, albumin, orosomucoid and alfa1-antitrypsin were also determined. In all patients the tumours contained significantly higher concentrations of CRBP (median = 185μg/g) tissue protein; range: 27–1,017μg/g) than normal mucosa (median = 14 μg/g tissue protein; range 6–97 μg/g). CRBP could not be detected in patient plasma. The tumour/normal mucosa CRBP concentration ratio showed a significant inverse correlation to a histopathological malignancy grade score evaluating the tumour-host relationship, suggesting that tumours with high CRBP relative to normal mucosa are biologically less aggressive. Tumour CRBP showed no correlation either to CRBP concentration in normal mucosa, or to plasma retinol or plasma retinol-binding protein concentration. CRBP concentration in normal mucosa, however, showed a significant correlation to plasma retinol-binding protein concentration. Most of the patients had low levels of plasma retinol and retinol-binding protein compared to matched controls. Whether this has any relationship to the development of the tumour, or whether the active inflammation induced by the cancer leads to a low plasma retinol concentration, is unknown.
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