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. 2006 Aug 15:6:207.
doi: 10.1186/1471-2407-6-207.

Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system

Affiliations

Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system

Dirk Vordermark et al. BMC Cancer. .

Abstract

Background: The tumor-associated glycoprotein osteopontin (OPN) is discussed as a plasma surrogate marker of tumor hypoxia and as an indicator of the presence of pleural mesothelioma in asbestos-exposed individuals. The clinical introduction of plasma OPN measurements requires the availability of a reliable enzyme-linked immunosorbence assay (ELISA).

Methods: We compared previously described and currently available ELISA systems on 88 archival plasma samples obtained from patients with head and neck or cervix cancer between 20 days before and 171 after the start of radiotherapy.

Results: Median (range) plasma OPN levels were 667 (148.8-2095) ng/ml and 9.8 (3.5-189.5) ng/ml for a previously described and a newly marketed assay, respectively. Although results for different assays were significantly correlated (r = 0.38, p < 0.05, Spearman rank test), between-assay factors ranged from 2.0 to 217.9 (median 74.6) in individual patients. OPN levels in cervix cancer patients were comparable to those of head and neck cancer patients.

Conclusion: Commercially available OPN ELISA systems produce different absolute plasma OPN levels, compromising a comparison of individual patient data with published results. However, different assays appear to have a similar capacity to rank patients according to plasma OPN level. A review of literature data suggests that plasma OPN levels measured even with identical ELISA systems can only be compared with caution.

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Figures

Figure 1
Figure 1
Osteopontin levels in individual plasma samples obtained from cervix or head and neck cancer patients undergoing radiotherapy. All samples were measured with two different ELISA systems, a newly introduced assay (A) and an older assay (B) marketed under two different names (see text). The results of both assays were significantly correlated (p < 0.05, Spearman rank test). For clarity, two data points with values of 80.5 and 189.5 ng/ml for assay A are not displayed.

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