Cancer diagnostics via ultrasensitive multiplexed detection of parathyroid hormone-related peptides with a microfluidic immunoarray
Otieno, Brunah A. ; Krause, Colleen E. ; Jones, Abby L. ; Kremer, Richard B. ; Rusling, James F.
Otieno, Brunah A.
Krause, Colleen E.
Jones, Abby L.
Kremer, Richard B.
Rusling, James F.
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Publication Date
2016-09-20
Type
Article
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Citation
Otieno, Brunah A. Krause, Colleen E.; Jones, Abby L.; Kremer, Richard B.; Rusling, James F. (2016). Cancer diagnostics via ultrasensitive multiplexed detection of parathyroid hormone-related peptides with a microfluidic immunoarray. Analytical Chemistry 88 (18), 9269-9275
Abstract
Parathyroid, hormone-related peptide (PTHrP) is recognized as the-Major causative agent of humoral hypercalcemia of malignancy (HHM). The paraneoplastic PTHrP has also been implicated in tumor progression and metastasis of many human cancers. Conventional PTHrP detection methods like immunoradiometric assay (IRMA) lack the sensitivity required to measure target peptide levels prior to, the, development of hypercalcemia. In general, sensitive, multiplexed peptide measurement by immunoassay represents challenges that we address in this paper. We describe here the first ultrasensitive multiplexed peptide assay to measure intact PTHrP 1-173 as well as circulating N-terminal and C-terminal peptide fragments. This Versatile approach should apply to almost any collection of peptides that are long enough to present binding sites for two antibodies. To target PTHrP, we employed a Microfluidic immunoarray featuring a chamber for online-Capture of the peptides from serum onto magnetic beads decorated with massive numbers of peptide-specific antibodies and enzyme labels. Magnetic bead-peptide conjugates were then washed and sent to a detection chamber housing an antibody-modified 8-electrode array fabricated by inkjet printing of gold nanoparticles. Limits of detection (LODS) of 150 aM (similar to 1000-fold lower than IRMA) in 5 mu L of serum were achieved for simultaneous detection of PTHrP isoforms and peptide fragments in 30 min. Good Correlation for patient samples was found with IRMA (n = 7),; r(2) = 0.99 assaying PTHrP 1-86 equiv fragments. Analysis by a receiver operating characteristic (ROC) plot;gave an area under the curve of 0.96, 80-83% clinical sensitivity, and 96-100% clinical specificity. Results suggest that PTHrP1-173 isoform and its Short C-terminal fragments are the predominant circulating forms of PTHrP. This new ultrasensitive) multiplexed assay for PTHrP and fragments is promising for clinical diagnosis, prognosis, and therapeutic monitoring froth early to advanced stage cancer patients and to examine underlying mechanisms of PTHrP overproduction.
Funder
Publisher
American Chemical Society (ACS)
Publisher DOI
10.1021/acs.analchem.6b02637
Rights
Attribution-NonCommercial-NoDerivs 3.0 Ireland