- Research article
- Open Access
- Open Peer Review
Plasma osteopontin levels in patients with head and neck cancer and cervix cancer are critically dependent on the choice of ELISA system
© Vordermark et al; licensee BioMed Central Ltd. 2006
- Received: 19 July 2006
- Accepted: 15 August 2006
- Published: 15 August 2006
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).
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.
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.
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.
- Neck Cancer
- Neck Cancer Patient
- ELISA System
- Tumor Oxygenation
Recent publications have renewed interest in the measurement of OPN, a tumor-associated glycoprotein secreted into bodily fluids, in the plasma of tumor patients. Plasma OPN level was shown by Le et al. to correspond with Eppendorf electrode measurements of tumor oxygenation in patients with head and neck cancer , suggesting a role for OPN as an endogenous marker of tumor hypoxia. In a landmark study, Overgaard et al. showed that only patients with high plasma levels of OPN (upper tertile) significantly benefitted from the addition of nimorazole, a hypoxic radiosensitizer, compared to standard radiotherapy in patients with head and neck cancer . OPN may therefore serve as a marker by which to select head and neck cancer patients for intensified, hypoxia-specific, treatment. It is currently unclear whether OPN may be similarly useful to predict tumor hypoxia in other entities in which oxygenation also has prognostic impact such as cervix cancer [3, 4]. Additional interest in OPN was raised by a prominent publication showing that in individuals with asbestos exposure, serum OPN levels can distinguish between those without cancer and those with pleural mesothelioma . A molecular mechanism for the intracellular accumulation of OPN under hypoxia has recently been described [6, 7], although secretion of OPN may require additional steps [8, 9].
A widespread application of OPN measurement in patient plasma or serum is dependent on the availability of reliable commercial enzyme-linked immunosorbent assay (ELISA) systems and may be affected by the problem of comparability between results of different assay systems. The choice of material, e. g. plasma vs. serum, and duration of storage may also affect the results of the ELISA.
To the authors' knowledge, the ELISA system utilized in the two reports on plasma OPN as a marker of tumor hypoxia in head and neck cancer [1, 2], is no longer commercially available We therefore performed a comparative analysis, using different commercial ELISA systems, of plasma OPN levels in 88 archival samples obtained from patients with head and neck cancer or cervix cancer at different timepoints before, during or after radiotherapy. Data were compared to published results for cancer and non-cancer patients as well as normal controls obtained with these ELISA systems.
Eighty-eight archival citrate plasma samples obtained from patients treated with radiotherapy between December of 1998 and May of 2000 at the Martin Luther University of Halle, Germany, and stored at -80°C, were now analyzed. Of these, 34 samples were from eleven patients with head and neck cancer (ten males, one female) and 54 were from 12 patients with cervix cancer. The median number of samples per patient was 4 (range 1 to 7). In head and neck cancer patients, a median of 2 samples (range 1 to 7) and in cervix cancer a median of 5.5 (range 1 to 7) samples were available. Samples were collected between 20 days before and 171 days after initiation of radiotherapy. Plasma sample collection was performed after written informed consent and approved by the local ethics committee
Plasma samples were analyzed in triplicate with different commercial ELISA systems, according to the respective manufacturers' instructions, as follows. Aliquots of all samples were analyzed with the currently available TiterZyme ELISA kit (Assay Designs, Ann Arbor, MI) introduced in July of 2005 by this manufacturer ("assay A"). Aliquots of all cervix cancer samples were additionally analyzed with the ELISA system previously marketed by this manufacturer under the same name which was used in previous publications on OPN as an endogenous hypoxia marker [1, 2]. This older version of the TiterZyme assay was designated "assay B1". According to this manufacturer, this assay (old TiterZyme, B1) was supplied by a third party producer (IBL, Gunma, Japan) who still markets this assay. All head and neck cancer samples were additionally analyzed with the current IBL assay which should be identical with the old TiterZyme assay and was therefore designated "assay B2". In summary, each sample was measured with one newly introduced ELISA assay (A) and one older assay (B) marketed under two different names (B1 and B2).
For each sample and assay, the mean of the triplicate measurement was calculated. The factor of the difference between assay B and assay A was determined for each sample. The correlation of results obtained with the newer assay (A) and the older assay (B) was analyzed by calculation of the Spearman-rank correlation coefficient (p < 0.05 regarded as significant).
Plasma osteopontin levels in head and neck cancer and cervix cancer patients as measured using two different ELISA systems.
individual factors (assay B/A)
mean ± SD
13.9 ± 21.0
786.0 ± 442.5
77.1 ± 41.4
(n = 88)
head and neck cancer
mean ± SD
16.1 ± 31.1
794.3 ± 467.2
76.3 ± 38.9
(n = 34)
mean ± SD
12.4 ± 11.0
780.7 ± 430.6
77.6 ± 43.3
(n = 54)
Although the time points at which samples were taken were not necessarily comparable between cervix and head and neck cancer patients, both assays indicated similar plasma OPN levels in these two tumor entities with median OPN levels (head and neck vs. cervix) of 10.4 vs. 9.5 ng/ml (assay A) and 650.2 vs 667.0 ng/ml (assay B).
OPN has been studied as a blood tumor marker since the mid-1990. Its expression level has been linked to the presence or extent of metastases or to clinical progression in several tumor entitities including breast, prostate and lung cancer [review in ]. Most of the earlier studies were performed with individually developed ELISA systems preventing comparison of results between centers.
Overview of osteopontin levels measured with commercially available ELISA systems in healthy controls, malignant and benign diseases.
patient group (n)
osteopontin mean ± SD (ng/ml)
osteopontin median (range) (ng/ml)
Assay Designs (B1)
head and neck cancer (54) von Hippel Lindau disease (31) healthy controls (15)
447 (261–843) 318 (233–461)
head and neck cancer (320)
nasopharyngeal cancer healthy controls
multiple sclerosis – relapsing patients (30)
healthy controls (10)
ovarian cancer (51)
healthy controls (28)
pleural mesothelioma (76)
asbestos-related non-malignant disease (69)
healthy controls (45)
133 ± 10
30 ± 3
20 ± 4
esophageal carcinoma (103)
ovarian cancer (51)
healthy controls (107)
ovarian cancer (38)
ovarian cancer, post-surgery (267)
healthy controls (67)
74 ± 116
147 ± 192
non-small lung cancer (158)
benign pulmonary disease (54)
healthy controls (25)
coronary artery disease (107)
healthy controls (71)
616 ± 308
443 ± 237
interstitial pneumonia (17)
healthy controls (20)
945 ± 256
156.7 ± 52.2
We therefore compared these different ELISA systems on a set of 88 archival plasma samples from patients treated with radiotherapy for head and neck or cervix cancer. The main finding was that the OPN levels determined with the new assay were much lower – by a mean factor of 77 – than measured with either form of the older assay. There was no uniform factor between old and new assay that would permit calculation of one from the other. In individual samples the factor ranged from 2 to 218. Nevertheless, OPN levels determined with the older and the newer assay were significantly correlated, suggesting that both assays should have a similar potential for selection of patients with poor-prognosis, hypoxic tumors. The fact that both forms of the older assay had similar mean factors compared to the new assay supports equivalence of the two. The large difference between old and new assay is well explained by differences in the epitope recognition sites of the respective capture antibodies provided with the ELISA assay kits and is, at least in part, anticipated by the range of standards provided with the respective kits (5–320 vs. 2–32 ng/ml). Various molecular forms of OPN have been described, resulting from RNA splicing, glycosylation, phosphorylation and proteolytic fragmentation, e. g. by thrombin . The use of various combinations of antibodies raised against four different portions of human OPN in a total of six separate ELISA systems has been shown to recognize distinct truncated or glycosylated forms of OPN .
A review of published data for the two forms of the old assay reveals that mean plasma OPN levels for healthy volunteers, for instance, vary substantially even when the identical ELISA kit is used (Table 2). This may in part be explained by the different type of material analyzed, such as EDTA plasma vs. citrate plasma vs. heparin plasma. Some authors did not specify the type of plasma obtained for OPN detection or analyzed serum samples, which apparently results in lower levels of OPN in healthy volunteers (Table 2). Conditions and duration of storage may also be critical. As highlighted by the literature review, many common non-malignant conditions, including coronary artery disease, interstitial pneumonia and other benign pulmonary diseases, multiple sclerosis or liver dysfunction may cause elevated plasma OPN values [14–17]. Some of these conditions may be present to a varying degree in groups of "healthy" volunteers, depending also on the age group selected.
As a consequence of the present results, the plasma OPN levels obtained with commercially available ELISA assay kits must be interpreted with caution. Differently optimized kits may be marketed under the same name such that comparison with published results may be compromised. It appears that even despite the use of the identical ELISA system, OPN levels are not reproducible in comparable patient cohorts between laboratories. For instance, the median values for untreated patients with advanced head and neck cancer were 450 ng/ml and 113 ng/ml in the two previously published series [1, 2]. However, elevated plasma OPN levels were consistently reported for different groups of cancer patients compared to controls, regardless of the type of assay used. For any multi-center investigation involving the measurement of plasma OPN, the collection and storage of plasma should be strictly regulated and the ELISA analysis should be centralized.
This work was supported in part by the Deutsche Forschungsgemeinschaft (to DV).
- Le QT, Sutphin PD, Raychaudhuri S, Yu SC, Terris DJ, Lin HS, Lum B, Pinto HA, Koong AC, Giaccia AJ: Identification of osteopontin as a prognostic plasma marker for head and neck squamous cell carcinomas. Clin Cancer Res. 2003, 9: 59-67.PubMedGoogle Scholar
- Overgaard J, Eriksen JG, Nordsmark M, Alsner J, Horsman MR, Danish Head and Neck Cancer Study Group: Plasma osteopontin, hypoxia, and response to the hypoxia sensitiser nimorazole in radiotherapy of head and neck cancer: results from the DAHANCA 5 randomised double-blind placebo-controlled trial. Lancet Oncol. 2005, 6: 757-764. 10.1016/S1470-2045(05)70292-8.View ArticlePubMedGoogle Scholar
- Dunst J, Kuhnt T, Strauss HG, Krause U, Pelz T, Koelbl H, Haensgen G: Anemia in cervical cancers: impact on survival, patterns of relapse, and association with hypoxia and angiogenesis. Int J Radiat Oncol Biol Phys. 2003, 56: 778-787. 10.1016/S0360-3016(03)00123-8.View ArticlePubMedGoogle Scholar
- Fyles A, Milosevic M, Hedley D, Pintilie M, Levin W, Manchul L, Hill RP: Tumor hypoxia has independent predictor impact only in patients with node-negative cervix cancer. J Clin Oncol. 2002, 20: 680-687. 10.1200/JCO.20.3.680.View ArticlePubMedGoogle Scholar
- Pass HI, Lott D, Lonardo F, Harbut M, Liu Z, Tang N, Carbone M, Webb C, Wali A: Asbestos exposure, pleural mesothelioma, and serum osteopontin levels. N Engl J Med. 2005, 353: 1564-1573. 10.1056/NEJMoa051185.View ArticlePubMedGoogle Scholar
- Sorensen BS, Hao J, Overgaard J, Vorum H, Honore B, Alsner J, Horsman MR: Influence of oxygen concentration and pH on expression of hypoxia induced genes. Radiother Oncol. 2005, 76: 187-193. 10.1016/j.radonc.2005.06.037.View ArticlePubMedGoogle Scholar
- Zhu Y, Denhardt DT, Cao H, Sutphin PD, Koong AC, Giaccia AJ, Le QT: Hypoxia upregulates osteopontin expression in NIH-3T3 cells via a Ras-activated enhancer. Oncogene. 2005, 24: 6555-6563.PubMedGoogle Scholar
- Lukacova S, Khalil AA, Overgaard J, Alsner J, Horsman MR: Relationship between radiobiological hypoxia in a C3H mouse mammary carcinoma and osteopontin levels in mouse serum. Int J Radiat Biol. 2006, 81: 937-944. 10.1080/09553000600567616.View ArticleGoogle Scholar
- Said HM, Katzer A, Flentje M, Vordermark D: Response of the plasma hypoxia marker osteopontin to in vitro hypoxia in human tumor cells. Radiother Oncol. 2005, 76: 200-205. 10.1016/j.radonc.2005.06.023.View ArticlePubMedGoogle Scholar
- Rittling SR, Chambers AF: Role of osteopontin in tumor progression. Brit J Cancer. 2004, 90: 1877-1881. 10.1038/sj.bjc.6601839.View ArticlePubMedPubMed CentralGoogle Scholar
- Nordsmark M, Bentzen SM, Rudat V, Brizel D, Lartigau E, Stadler P, Becker A, Adam M, Molls M, Dunst J, Terris DJ, Overgaard J: Prognostic value of tumor oxygenation in 397 head and neck tumors after primary radiation therapy. An international multi-center study. Radiother Oncol. 2005, 77: 18-24. 10.1016/j.radonc.2005.06.038.View ArticlePubMedGoogle Scholar
- Denhardt DT, Guo X: Osteopontin: a protein with diverse functions. FASEB J. 1993, 7: 1475-1482.PubMedGoogle Scholar
- Kon S, Maeda M, Segawa T, Hagiwara Y, Horikoshi Y, Chikuma S, Tanaka K, Rashid MM, Inobe M, Chambers AF, Uede T: Antibodies to different peptides in osteopontin reveal complexities in the various secreted forms. J Cell Biochem. 2000, 77: 487-498. 10.1002/(SICI)1097-4644(20000601)77:3<487::AID-JCB13>3.0.CO;2-8.View ArticlePubMedGoogle Scholar
- Arai M, Yokosuka O, Kanda T, Fukai K, Imazeki F, Murumatsu M, Seki N, Miyazaki M, Ochiai T, Hirasawa H, Saisho H: Serum osteopontin levels in patients with acute liver dysfunction. Scand J Gastroenterol. 2006, 41: 102-110. 10.1080/00365520510024061.View ArticlePubMedGoogle Scholar
- Kadota J, Mizunoe S, Mito K, Mukae H, Yoshioka S, Kawakami K, Koguchi Y, Fukushima K, Kon S, Kohno S, Saito A, Uede T, Nasu M: High plasma concentrations of osteopontin in patients with interstitial pneumonia. Respir Med. 2005, 99: 111-117. 10.1016/j.rmed.2004.04.018.View ArticlePubMedGoogle Scholar
- Ohmori R, Momiyama Y, Taniguchi H, Takahashi R, Kusuhara M, Nakamura H, Ohsuzu F: Plasma osteopontin levels are associated with the presence and extent of coronary artery disease. Atherosclerosis. 2003, 170: 333-337. 10.1016/S0021-9150(03)00298-3.View ArticlePubMedGoogle Scholar
- Vogt MH, Lopatinskaya L, Smits M, Polman CH, Nagelkerken L: Elevated osteopontin levels in active relapsing-remitting multiple sclerosis. Ann Neurol. 2003, 53: 819-822. 10.1002/ana.10606.View ArticlePubMedGoogle Scholar
- Wong TS, Kwong DL, Sham J, Wei WI, Kwong YL, Yuen AP: Elevation of plasma osteopontin level in patients with undifferentiated nasopharyngeal carcinoma. Eur J Surg Oncol. 2005, 31: 555-558. 10.1016/j.ejso.2005.01.005.View ArticlePubMedGoogle Scholar
- Mor G, Visintin I, Lai Y, Zhao H, Schwartz P, Rutherford T, Yue L, Bray-Ward P, Ward DC: Serum protein markers for early detection of ovarian cancer. Proc Natl Acad Sci USA. 2005, 102: 7677-7682. 10.1073/pnas.0502178102.View ArticlePubMedPubMed CentralGoogle Scholar
- Shimada Y, Watanabe G, Kawamura J, Soma T, Okabe M, Ito T, Inoue H, Kondo M, Mori Y, Tanaka E, Imamura M: Clinical significance of osteopontin in esophageal squamous cell carcinoma: comparison with common tumor markers. Oncol. 2005, 68: 285-92. 10.1159/000086961.View ArticleGoogle Scholar
- Kim JH, Skates SJ, Uede T, Wong KK, Schorge JO, Feltmate CM, Berkowitz RS, Cramer DW, Mok SC: Osteopontin as a potential diagnostic biomarker for ovarian cancer. JAMA. 2002, 287: 1671-1679. 10.1001/jama.287.13.1671.View ArticlePubMedGoogle Scholar
- Schorge JO, Drake RD, Lee H, Skates SJ, Rajanbabu R, Miller DS, Kim JH, Cramer DW, Berkowitz RS, Mok SC: Osteopontin as an adjunct to CA125 in detecting recurrent ovarian cancer. Clin Cancer Res. 2004, 10: 3474-3478. 10.1158/1078-0432.CCR-03-0365.View ArticlePubMedGoogle Scholar
- Brakora KA, Lee H, Yusuf R, Sullivan L, Harris A, Colella T, Seiden MV: Utility of osteopontin as a biomarker in recurrent epithelial ovarian cancer. Gynecol Oncol. 2004, 93: 361-365. 10.1016/j.ygyno.2004.01.050.View ArticlePubMedGoogle Scholar
- Hu Z, Lin D, Yuan J, Xiao T, Zhang H, Sun W, Han M, MA Y, Di X, Gao M, Ma J, Zhang J, Cheng S, Gao Y: Overexpression of osteopontin is associated with more aggressive phenotypes in human non-small cell lung cancer. Clin Cancer Res. 2005, 11: 4646-4652. 10.1158/1078-0432.CCR-04-2013.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/6/207/prepub
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