Coexpression of hypoxia-inducible factor-1α and glucose transporter-1 is associated with poor prognosis in oral squamous cell carcinoma patients

被引:57
作者
Eckert, Alexander W. [1 ]
Lautner, Matthias H. W. [1 ]
Schuetze, Andreas [1 ]
Taubert, Helge [1 ]
Schubert, Johannes [1 ]
Bilkenroth, Udo [2 ]
机构
[1] Univ Halle Wittenberg, Dept Oral & Maxillofacial Plast Surg, D-06120 Halle, Germany
[2] Inst Pathol, Eisleben, Germany
关键词
glucose transporter-1; head and neck cancer; hypoxia-inducible factor-1 alpha; oral squamous cell carcinoma; EMBRYONIC STEM-CELLS; NECK-CANCER; GLUCOSE-TRANSPORT; CA-IX; HEAD; RADIOTHERAPY; EXPRESSION; MARKERS; TUMOR; OVEREXPRESSION;
D O I
10.1111/j.1365-2559.2011.03806.x
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Aims: To study whether coexpression of the two hypoxia-related proteins hypoxia-inducible factor (HIF)-1 alpha and glucose transporter (GLUT)-1 has prognostic relevance in oral squamous cell carcinomas (OSCCs). Methods and results: Eighty-two OSCC samples were analysed for expression levels of HIF-1 alpha and GLUT-1 by immunohistochemistry. Protein expression was assessed with an immunoreactive score system, and the correlations between gene expression and both clinical and pathohistological parameters were examined. Overexpression of either GLUT-1 or HIF-1 alpha was associated with poor disease-specific survival in OSCC patients. Multivariate Cox proportional-hazards regression analysis revealed that increased expression of HIF-1 alpha was significantly associated with disease-specific survival (relative risk = 3.24, P = 0.024), as compared with the group with a low level of expression. Coexpression of HIF-1 alpha and GLUT-1 was additively and significantly associated with adverse prognoses in patients with OSCC. Patients whose tumours had increased levels of expression of both HIF-1 alpha and GLUT-1 were found to have a 5.13-fold increased risk of tumour-related death (P = 0.017). Conclusions: Coexpression of high levels of HIF-1 alpha and GLUT-1 is significantly correlated with prognosis in OSCC patients, suggesting that the coexpression of these proteins can be used as both an early diagnostic and independent prognostic marker.
引用
收藏
页码:1136 / 1147
页数:12
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