Enhanced protein profiling arrays with ELISA-based amplification for high-throughput molecular changes of tumor patients' plasma.

Abstract

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.

• Authors: Ruochun Huang, Ying Lin, Qian Shi, Lisa Flowers, Sumathi Ramachandran, Ira R Horowitz, Sampath Parthasarathy, Ruo-Pan Huang
• Journal: Clinical cancer research : an official journal of the American Association for Cancer Research (Clin Cancer Res) Vol. 10 Issue 2 Pg. 598-609 (Jan 15 2004) ISSN: 1078-0432 [Print] United States
• PMID: 14760082 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Immunoglobulin G
• Interleukin-8
• Platelet-Derived Growth Factor
• Vascular Endothelial Growth Factor A
• Epidermal Growth Factor
• Biotin
• angiogenin
• Ribonuclease, Pancreatic

Topics

• Adolescent
• Adult
• Aged
• Aged, 80 and over
• Biotin (chemistry)
• Cell Line, Tumor
• Cluster Analysis
• Enzyme-Linked Immunosorbent Assay
• Epidermal Growth Factor (biosynthesis, metabolism)
• Female
• Genital Neoplasms, Female (genetics, metabolism)
• Humans
• Immunoglobulin G (chemistry)
• Interleukin-8 (biosynthesis, metabolism)
• Luminescent Measurements
• Microscopy, Fluorescence
• Middle Aged
• Multigene Family
• Neoplasms (metabolism)
• Neovascularization, Pathologic
• Oligonucleotide Array Sequence Analysis
• Platelet-Derived Growth Factor (biosynthesis, metabolism)
• Protein Array Analysis (methods)
• Ribonuclease, Pancreatic (biosynthesis)
• Sensitivity and Specificity
• Tissue Distribution
• Vascular Endothelial Growth Factor A (biosynthesis, metabolism)