Tissue Expression of Hypoxia-Inducible Factor 1 Alpha (HIF-1A) in Wilms Tumor
INTRODUCTION: The hypoxia- inducible factor (HIF) is an alpha (α)/ beta (β) heterodimeric DNA binding complex and directs an extensive transcriptional response involving the induction of genes relevant to tumor progression, such as angiogenesis, glucose/ energy metabolism, cellular growth, metastasi...
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Main Authors: | , , , , |
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Format: | Book |
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Galenos Publishing House,
2019-03-01T00:00:00Z.
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Summary: | INTRODUCTION: The hypoxia- inducible factor (HIF) is an alpha (α)/ beta (β) heterodimeric DNA binding complex and directs an extensive transcriptional response involving the induction of genes relevant to tumor progression, such as angiogenesis, glucose/ energy metabolism, cellular growth, metastasis, and apoptosis. HIF-1A has also emerged as an attractive target for cancer therapy. The aim of this study is to investigate the association between tissue HIF-1A expression, prognostic significance and the clinicopathologic features of Wilms tumors. METHODS: Nuclear HIF-1A expression in 53 tissue samples harvested from children with Wilms tumor and its relationship with prognostic parameters were evaluated. RESULTS: Tissue samples of 53 cases (male, n=25: 47.2 %, and female, n=28: 52.8 %) with Wilms tumor with a mean age of 3.21+-2 years were analyzed. Mean tumor size, and weight of kidneys were 9.1 +- 2.9 cm in diameter and 474.5+-310.7 gr, respectively. Thirteen (24.5%) cases were in stage I, 20 (37.7%) in stage II, 7 (14%) in stage III, and 6 (11.3%) stage IV. Forty-two cases were alive (79.2%), while 11 cases (20.8%) were deceased. Mean overall survival time was 65.3+-40.2 (2- 148) months. Nuclear HIF-1A expression was positive in only 3 viably tumors (5.7%), while it was negative or cytoplasmic artificially positive in other tumors. Statistically, there was no any correlation between HIF-1A expression and other prognostic factors. DISCUSSION AND CONCLUSION: In contrast to other reports, this study indicated that HIF-1A expression is not associated with development and pathogenesis of Wilms Tumor. |
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Item Description: | 2822-4469 10.5222/buchd.2018.53386 |