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Updated: May 23, 2026

12:03
In Vivo Model for Testing Effect of Hypoxia on Tumor Metastasis
Published on: December 9, 2016
Prognostic impacts of hypoxic markers in soft tissue sarcoma
Eivind Smeland1, Thomas K Kilvaer, Sveinung Sorbye
1Institute of Clinical Medicine, University of Tromso, 9037 Tromso, Norway.
Sarcoma
|March 29, 2012
Summary
Hypoxia-induced factor GLUT-1 (glucose transporter 1) is a significant predictor of poor survival in soft tissue sarcomas (non-GIST STS). High GLUT-1 expression indicates a worse prognosis for disease-specific survival in these patients.
Area of Science:
- Oncology
- Pathology
- Molecular Biology
Background:
- Soft tissue sarcomas (STS) are a heterogeneous group of cancers.
- Hypoxia, a low-oxygen environment, plays a role in tumor progression.
- Hypoxia-induced factors (HIFs) and their downstream targets are implicated in cancer survival.
Purpose of the Study:
- To investigate the prognostic value of hypoxia-related markers in non-gastrointestinal stromal tumor soft tissue sarcomas (non-GIST STS).
- Specifically, to assess the impact of hypoxia-induced factors (HIFαs) 1 and 2, glucose transporter 1 (GLUT-1), and carbonic anhydrase IX (CAIX).
Main Methods:
- Tissue microarrays were constructed from 206 non-GIST STS patient samples.
- Immunohistochemistry (IHC) was employed to evaluate the expression levels of hypoxic markers.
- Univariate and multivariate survival analyses were performed.
Main Results:
- Univariate analysis showed significant correlations between GLUT-1 and HIF-2α expression and poor disease-specific survival (DSS).
- Multivariate analysis identified high GLUT-1 expression as an independent negative prognostic indicator for DSS (HR 1.7, P = 0.021).
- HIF-2α did not remain a significant independent prognostic factor in the multivariate model.
Conclusions:
- Glucose transporter 1 (GLUT-1) is a significant independent negative prognostic factor in non-GIST STS.
- High GLUT-1 expression is associated with reduced disease-specific survival.
- These findings highlight GLUT-1 as a potential therapeutic target in non-GIST STS.
