A targeted isotope dilution mass spectrometry assay for osteopontin quantification in plasma of metastatic breast cancer patients

• Published in: PloS one Vol. 18; no. 6; p. e0281491
• Main Authors: Leslie, Andrew, Teh, Evelyn, Druker, Arik, Pinto, Devanand M
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 29.06.2023; Public Library of Science (PLoS)
• Subjects: Antibodies; Assaying; Biology and Life Sciences; Biomarkers; Blood plasma; Breast cancer; Care and treatment; Cell adhesion; Chromatography; Dilution; Enzyme-linked immunosorbent assay; Epitopes; Evaluation; Health aspects; Immune system; Isoforms; Isotopes; Mass spectrometry; Mass spectroscopy; Medical prognosis; Medicine and Health Sciences; Metastases; Metastasis; Methods; Monoclonal antibodies; Osteopontin; Patient outcomes; Patients; Peptides; Plasma; Post-translation; Proteins; Research and Analysis Methods; Scientific imaging; Sensitivity; Tumor cells; Tumors; United Kingdom; Canada; Nova Scotia Canada
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0281491

Osteopontin (OPN) is a secreted glycophosphoprotein that derives its name from its high abundance in bone and secretion by osteoblasts. It is also secreted by a number of immune cells and, therefore, is present in human plasma at nanogram per millilitre levels where it affects cell adhesion and motility. OPN is involved in several normal physiological processes; however, OPN dyregulation leads to overexpression by tumor cells leading to immune evasion and increased metastasis. Plasma OPN is primarily measured by enzyme-linked immunosorbent assay (ELISA). However, due to the complexity of the various OPN isoforms, conflicting results have been obtained on the use of OPN as a biomarker even in the same disease condition. These discrepant results may result from the difficulty in comparing ELISA results obtained with different antibodies that target unique OPN epitopes. Mass spectrometry can be used to quantify proteins in plasma and, by targeting OPN regions that do not bear post-translational modifications, may provide more consistent quantification. However, the low (ng/mL) levels in plasma present a significant analytical challenge. In order to develop a sensitive assay for plasma OPN, we explored a single-step precipitation method using a recently developed spin-tube format. Quantification was performed using isotope-dilution mass spectrometry. The concentration detection limit of this assay was 39 ± 15 ng/mL. The assay was applied to the analysis of plasma OPN in metastatic breast cancer patients, where levels from 17 to 53 ng/mL were detected. The sensitivity of the method is higher than previously published methods and sufficient for OPN detection in large, high grade tumors but still requires improvement in sensitivity to be widely applicable.
NRC publication: Yes