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Nano-Biomarker Arrays for Cancer Diagnostics
(2012 -
Present)
Investigator:
Bernard Munge,
Salve
Regina
University Mentor: James
Rusling, University of Connecticut
Abstract:
Rapid, extremely sensitive and accurate
biosensor arrays for clinical measurements of biomarker proteins for
early detection and monitoring of cancer are critically important and
will lead to inexpensive devices for reliable on-the-spot cancer
diagnosis, improved therapeutic outcomes at lower costs, decreased
patient stress, and new targeted therapies. Such devices will also
provide tools for a better fundamental understanding of disease
progression, and enable biomarker-based monitoring of therapy. The major
goal of this project is to develop nanomaterial-based arrays to measure
collections of early cancer biomarker proteins for cutaneous T cell
carcinoma and tobacco related cancers. Proposed devices feature
nanostructured electrode surfaces with capture antibodies attached. The
nanostructured electrodes will be fabricated into immunosensor arrays
featuring electrochemical detection of biomarker proteins via enzyme
labels on secondary antibodies. Biomarkers are molecules in the body
that increase in concentration during the onset of cancer, and can be
used for early cancer detection. Biosensor arrays are devices that can
measure a number of biomarkers in patients at low cost. Biosensor arrays
for this task are not available and will be developed and used to
measure protein biomarkers and establish correlations for a broad range
of patients. The major specific objectives of this project are 3-fold.
(1) Develop methodology employing nanostructured electrodes and signal
amplification strategy for amperometric antibody-antigen immunological
assays for multiple cancer biomarker proteins (2) Develop bioelectronic
arrays for protein biomarkers (3) Quantify Specific Biomarkers. Our
initial targets are cancer biomarker proteins, mutant P53, IL-6, IL-8,
CD25, and CD30. After successful development, optimization, and
validation, we will use these biosensors to examine cancer biomarker
levels (mutant p53, IL-6 and IL-8) in serum of smokers and nonsmokers.
This project will enable rapid assessment of important correlations
between biomarker patterns and tobacco-related cancer. It will also lead
to point-of-care arrays for cancer detection, tobacco-related risk
assessment, and foster new cancer preventing treatments tailored to
individual patients. |