Hypoxia-inducible factor-1alfa mRNA and protein levels in renal cell carcinoma
Anders Lidgren, Anders Bergh, Kjell Grankvist, Gudrun Lindh, Börje Ljungberg
Abstract
Anders Lidgren, Anders Bergh, Kjell Grankvist, Gudrun Lindh, Börje Ljungberg
Abstract
AIM: Angiogenesis plays a central role in the growth of a tumor. The hypoxiainducible factor 1α (HIF-1α) is a regulated subunit of HIF-1, a key factor that carries fundamental features in angiogenesis and tumor progression. Renal cell carcinoma (RCC) is highly vascularized with a variable clinical outcome, having specific genetic alterations in different RCC types. This study investigated HIF-1α mRNA and protein expression in relation to RCC type and clinicopathological variables including clinical stage and survival. METHODS: Quantitative analysis of HIF-1α mRNA expression in 202 patients including 168 clear cell (cRCC), 23 papillary (pRCC) and 11 chromophobe RCCs. Additionally, 49 samples from non-malignant corresponding kidney cortex were analysed. Comparative analysis of HIF-1α protein expression was performed by immunohistochemistry of tissue microarray. RESULTS: HIF-1α mRNA levels were significantly lower in cRCC compared with pRCC (P = 0.001) and kidney cortex (P < 0.001). In cRCC, HIF-1α mRNA was correlated to gender and age. For pRCC there was no correlation between HIF-1α mRNA and tumor stage, nuclear grade, age, tumor size or gender. HIF-1α mRNA expression was inversely related to HIF-1α protein levels in pRCC (P = 0.041) but not significantly in cRCC (P = 0.075). CONCLUSION: HIF-1α mRNA levels were significantly lower in cRCC copmpared with kidney cortex and the other RCC types. High HIF-1α protein expression appeared to suppress HIF-1α mRNA expression, distressing the HIF-1 pathway in RCC.
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AIM: Angiogenesis plays a central role in the growth of a tumor. The hypoxiainducible factor 1α (HIF-1α) is a regulated subunit of HIF-1, a key factor that carries fundamental features in angiogenesis and tumor progression. Renal cell carcinoma (RCC) is highly vascularized with a variable clinical outcome, having specific genetic alterations in different RCC types. This study investigated HIF-1α mRNA and protein expression in relation to RCC type and clinicopathological variables including clinical stage and survival. METHODS: Quantitative analysis of HIF-1α mRNA expression in 202 patients including 168 clear cell (cRCC), 23 papillary (pRCC) and 11 chromophobe RCCs. Additionally, 49 samples from non-malignant corresponding kidney cortex were analysed. Comparative analysis of HIF-1α protein expression was performed by immunohistochemistry of tissue microarray. RESULTS: HIF-1α mRNA levels were significantly lower in cRCC compared with pRCC (P = 0.001) and kidney cortex (P < 0.001). In cRCC, HIF-1α mRNA was correlated to gender and age. For pRCC there was no correlation between HIF-1α mRNA and tumor stage, nuclear grade, age, tumor size or gender. HIF-1α mRNA expression was inversely related to HIF-1α protein levels in pRCC (P = 0.041) but not significantly in cRCC (P = 0.075). CONCLUSION: HIF-1α mRNA levels were significantly lower in cRCC copmpared with kidney cortex and the other RCC types. High HIF-1α protein expression appeared to suppress HIF-1α mRNA expression, distressing the HIF-1 pathway in RCC.
Key concepts: Papillary renal cell carcinomas, Biology, Hypoxia-inducible factors, Immunohistochemistry, Angiogenesis, Renal cell carcinoma, Clear cell renal cell carcinoma, Tissue microarray