
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Molecular Oncology, Markers, Clinical Correlates |
Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, Georgia
Purpose: The purpose of this study is to develop a high-throughput approach to detect protein expression from hundreds and thousands of samples and to apply this technology to profile circulating angiogenic factor protein levels in patients with gynecological tumors.
Experimental Design: Analytes containing a mixture of protein are immobilized onto antibody-coated surface of support in array format. The presence of protein in analytes is detected with biotin-labeled antibody coupled with an enhanced chemiluminescence or fluorescence detection system. The exact amount of protein can be quantitatively measured. The expression levels of five angiogenic factors (angiogenin, interleukin 8, vascular endothelial growth factor, platelet-derived growth factor, and epidermal growth factor) from 157 samples were quantitatively measured using this novel protein array technology and were statistically analyzed. The expression patterns of angiogenic factors were analyzed using two-way hierarchical cluster analysis approach.
Results: A novel protein array technology, which can simultaneously and quantitatively measure few protein levels from hundreds and thousands of samples was developed. Only minute amounts of sample are required for the assay. This approach also features high sensitivity and specificity. Using this novel protein array approach, we analyzed the plasma expression levels of five angiogenic factors in 137 patients diagnosed with a tumor and 20 controls. Statistical analysis reveals different expression levels of angiogenic factors between patients and controls. Cluster analysis suggests a possible classification of normal subjects from patients.
Conclusions: Enhanced protein profiling arrays provide a high-throughput and sensitive system to detect one or few protein from hundreds and thousands of samples. Such an approach should have broad application in biomedical discovery.
This article has been cited by other articles:
![]() |
M. Sanchez-Carbayo Antibody Arrays: Technical Considerations and Clinical Applications in Cancer Clin. Chem., September 1, 2006; 52(9): 1651 - 1659. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. B. Haab Using Array-Based Competitive and Noncompetitive Immunoassays Am. Assoc. Cancer Res. Educ. Book, April 1, 2006; 2006(1): 148 - 154. [Full Text] [PDF] |
||||
![]() |
R. Orchekowski, D. Hamelinck, L. Li, E. Gliwa, M. VanBrocklin, J. A. Marrero, G. F. Vande Woude, Z. Feng, R. Brand, and B. B. Haab Antibody Microarray Profiling Reveals Individual and Combined Serum Proteins Associated with Pancreatic Cancer Cancer Res., December 1, 2005; 65(23): 11193 - 11202. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. B. Haab Antibody Arrays in Cancer Research Mol. Cell. Proteomics, April 1, 2005; 4(4): 377 - 383. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. W. Jacobson Comprehensive Molecular Analysis of Human Specimens Am. Assoc. Cancer Res. Educ. Book, April 1, 2005; 2005(1): 311 - 314. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Cancer Research | Clinical Cancer Research |
| Cancer Epidemiology Biomarkers & Prevention | Molecular Cancer Therapeutics |
| Molecular Cancer Research | Cancer Prevention Research |
| Cancer Prevention Journals Portal | Cancer Reviews Online |
| Annual Meeting Education Book | Meeting Abstracts Online |