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Glucose transporter‐1 expression in renal cell carcinoma and its correlation with hypoxia inducible factor‐1α

OBJECTIVE To evaluate transcription factor hypoxia inducible factor‐1α (HIF‐1α) activity, by analysing a target gene for HIF‐1α, glucose transporter‐1 (GLUT‐1), using a tissue microarray (TMA) in different types of renal cell carcinoma (RCC, a tumour with a variable clinical course, partly due to an...

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Published in:BJU international 2008-02, Vol.101 (4), p.480-484
Main Authors: Lidgren, Anders, Bergh, Anders, Grankvist, Kjell, Rasmuson, Torgny, Ljungberg, Börje
Format: Article
Language:English
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Summary:OBJECTIVE To evaluate transcription factor hypoxia inducible factor‐1α (HIF‐1α) activity, by analysing a target gene for HIF‐1α, glucose transporter‐1 (GLUT‐1), using a tissue microarray (TMA) in different types of renal cell carcinoma (RCC, a tumour with a variable clinical course, partly due to angiogenic activity), as angiogenesis is important for tumour progression and metastatic spread, and is activated by hypoxia. PATIENTS AND METHODS GLUT‐1 and HIF‐1α expressions were semiquantitatively analysed using immunohistological staining of a prepared TMA, using samples from 187 patients, including 148 with conventional, 26 with papillary and 13 with chromophobe RCC. RESULTS GLUT‐1 staining was found mainly in the cytoplasm. The tumours were subdivided into GLUT −1LOW and GLUT‐1HIGH, based on staining intensity. There was a significant difference in GLUT‐1 expression between RCC types (P 
ISSN:1464-4096
1464-410X
1464-410X
DOI:10.1111/j.1464-410X.2007.07238.x