Expression of hypoxia-inducible factor-1α in esophageal squamous cell carcinoma
Article first published online: 16 MAR 2005
DOI: 10.1111/j.1349-7006.2005.00025.x
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How to Cite
Matsuyama, T., Nakanishi, K., Hayashi, T., Yoshizumi, Y., Aiko, S., Sugiura, Y., Tanimoto, T., Uenoyama, M., Ozeki, Y. and Maehara, T. (2005), Expression of hypoxia-inducible factor-1α in esophageal squamous cell carcinoma. Cancer Science, 96: 176–182. doi: 10.1111/j.1349-7006.2005.00025.x
Publication History
- Issue published online: 16 MAR 2005
- Article first published online: 16 MAR 2005
- (Received September 6, 2004/Revised December 21, 2004/Accepted December 24, 2004/Online publication March 15, 2005)
- Abstract
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Hypoxia-inducible factor-1 (HIF-1) is a transcription factor that plays an important role in tumor growth and metastasis by regulating energy metabolism and inducing angiogenesis. Elevated levels of HIF-1α, a subunit of HIF-1, are noted in various malignant tumors, but it is unclear whether this is so in esophageal carcinoma. The purpose of this study was to evaluate the implications of HIF-1α expression in esophageal squamous cell carcinoma. In 215 patients with esophageal carcinoma, we examined immunoreactivity for HIF-1α protein, vascular endothelial growth factor (VEGF) protein and p53 protein. In 38 patients, we examined the expression of HIF-1α messenger ribonucleic acid (mRNA) (using the semiquantitative reverse transcriptase-polymerase chain reaction [RT-PCR]). A positive HIF-1α protein expression was recognized in 95% of the patients, and was strongly apparent within both the nuclei and/or cytoplasm of tumor cells. The proportion of patients in the ‘high score’ group for HIF-1α protein expression increased significantly with increasing VEGF protein expression. Immunoreactivity for HIF-1α protein was found to have a significant effect on disease-free survival rate in our univariate analysis, but no effect on overall survival rate. In RT-PCR, HIF-1α mRNA scores correlated significantly with scores for HIF-1α protein expression, but not with any clinicopathologic factor or either of the survival rates. The detection of HIF-1α protein and mRNA would appear to offer limited information as to progression and prognosis in esophageal carcinoma. (Cancer Sci 2005; 96: 176–182)

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