Elevated tumor and serum levels of the hypoxia-associated protein osteopontin are associated with prognosis for soft tissue sarcoma patients
By: Matthias Bache , Matthias Kappler , Henri Wichmann , Swetlana Rot , Antje Hahnel , Thomas Greither , Harun M Said , Matthias Kotzsch , Peter Wurl , Helge Taubert and Dirk Vordermark

BMC Cancer 2010, 10:132 doi:10.1186/1471-2407-10-132
Published: 8 April 2010

Abstract (Provisional)

Background

Osteopontin (OPN) overexpression is correlated with a poor prognosis for tumor patients. However, only a few studies investigated the prognostic impact of expression of OPN in soft tissue sarcomas (STS) yet.

Methods

This study is based on tumor and serum samples from 93 adult STS patients. We investigated OPN protein levels in serum (n=86) and tumor tissue (n=80) by ELISA and OPN mRNA levels in tumor tissue (n=68) by quantitative real-time PCR.

Results

No correlation was found between OPN levels in serum and tumor tissue. Moreover, an elevated OPN protein level in the serum was significantly associated with clinical parameters such as higher stage (p=0.004), higher grade (p=0.003), subtype (p=0.002) and larger tumor size (p=0.03). OPN protein levels in the tumor tissue were associated with higher stage (p=0.06), higher grade (p=0.003), subtype (p=0.07) and an increased rate of relapse (p=0.02). In addition, using a Cox's proportional hazards regression model, we found that an elevated OPN protein level in the serum and tumor tissue extracts is a significant negative prognostic factor for patients with STS. The relative risks of tumor-related death were 2.2 (p<0.05) and 3.7 (p=0.01), respectively.

Conclusion

Our data suggest OPN protein in serum as well as in tumor tissue extracts is an important prognostic factor for soft tissue sarcoma patients.

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* Albert Einstein College of Medicine has been
awarded Acceditation with Commendation by
the ACCME

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