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Overexpression of hypoxia-inducible-factor 1α(HIF-1α) in oesophageal squamous cell carcinoma correlates with lymph node metastasis and pathologic stage
The purpose of this study is to investigate the clinical and histopathologic significance of hypoxia-inducible-factor 1 α (HIF-1 α ) expression in oesophageal squamous cell carcinoma. One hundred and thirty surgically resected specimens of OSCC were immunohistochemically assessed for HIF-1 α express...
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Published in: | British journal of cancer 2003-09, Vol.89 (6), p.1042-1047 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The purpose of this study is to investigate the clinical and histopathologic significance of hypoxia-inducible-factor 1
α
(HIF-1
α
) expression in oesophageal squamous cell carcinoma. One hundred and thirty surgically resected specimens of OSCC were immunohistochemically assessed for HIF-1
α
expression with monoclonal antibody. High HIF-1
α
immunostaining was detected in 40 specimens. The percentage of high HIF-1
α
expression cases increased with tumour stage according to pTNM system. High HIF-1
α
expression correlated with pTNM stage, depth of tumour invasion, lymph node metastasis, distant metastasis, lymphatic invasion and positive surgical margin. The overall survival rate was worse in patients with high HIF-1
α
pattern than in patients with low-expression pattern. Univariate analyses identified high HIF-1
α
positivity, depth of tumour invasion, lymph node metastasis, distant metastasis, lymphatic invasion, and a positive surgical margin as risk factors. Multivariate analyses indicated that depth of tumour invasion, lymph node metastasis and positive surgical margin, but not HIF-1
α
, were independent prognostic factors. Survival in patients with a high HIF-1
α
expression was significantly worse than in those with low expression in patient treated with adjuvant therapy. |
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ISSN: | 0007-0920 1532-1827 |
DOI: | 10.1038/sj.bjc.6601186 |