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• W2016207781 abstract "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 −1 LOW and GLUT‐1 HIGH , based on staining intensity. There was a significant difference in GLUT‐1 expression between RCC types ( P < 0.05). In conventional RCC, GLUT‐1 had no correlation with clinicopathological variables. By contrast there was a correlation with tumour stage in papillary RCC. There was an insignificant trend to better survival of patients with GLUT‐1 LOW expression in both conventional and papillary RCC. GLUT‐1 correlated significantly ( P = 0.008) with HIF‐1α. CONCLUSIONS Most patients with conventional RCC had GLUT‐1 HIGH staining and there was a significant correlation with HIF‐1α. In papillary RCC, GLUT‐1 expression was associated with stage; GLUT‐1 expression was significantly higher in conventional RCC than in papillary and chromophobe RCC. GLUT‐1 LOW in both papillary and conventional RCC appeared to correspond with a better prognosis." @default.
• W2016207781 created "2016-06-24" @default.
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• W2016207781 date "2007-10-17" @default.
• W2016207781 modified "2023-10-16" @default.
• W2016207781 title "Glucose transporter-1 expression in renal cell carcinoma and its correlation with hypoxia inducible factor-1α" @default.
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• W2016207781 doi "https://doi.org/10.1111/j.1464-410x.2007.07238.x" @default.
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