Assessment of vascular endothelial growth factor in formalin fixed, paraffin embedded colon cancer specimens by means of a well-based reverse phase protein array

• Published in: Proteome science Vol. 12; no. 1; p. 27
• Main Authors: Chung, Joon-Yong, Braunschweig, Till, Hong, Seung-Mo, Kwon, David S, Eo, Soo-Heang, Cho, HyungJun, Hewitt, Stephen M
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 13-05-2014; BioMed Central
• Subjects: Antigens; Colon; Comparative analysis; Complications and side effects; Development and progression; Experiments; Formaldehyde; Genetic aspects; Health aspects; Medical research; Medicine, Experimental; Metastasis; Methodology; Molecular weight; Pathology; Patient outcomes; Protein expression; Proteins; Risk factors; Rodents; Vascular endothelial growth factor; Immunohistochemistry; Reverse-phase protein array; Colon cancer; Formalin-fixed paraffin-embedded; Vascular endothelial growth factor
• ISSN: 1477-5956; 1477-5956
• DOI: 10.1186/1477-5956-12-27

Vascular endothelial growth factor (VEGF) is a critical pro-angiogenic factor, found in a number of cancers, and a target of therapy. It is typically assessed by immunohistochemistry (IHC) in clinical research. However, IHC is not a quantitative assay and is rarely reproducible. We compared VEGF levels in colon cancer by IHC and a quantitative immunoassay on proteins isolated from formalin fixed, paraffin embedded tissues.
VEGF expression was studied by means of a well-based reverse phase protein array (RPPA) and immunohistochemistry in 69 colon cancer cases, and compared with various clinicopathologic factors. Protein lysates derived from formalin fixed, paraffin embedded tissue contained measurable immunoreactive VEGF molecules. The VEGF expression level of well differentiated colon cancer was significantly higher than those with moderately and poorly differentiated carcinomas by immunohistochemistry (P = 0.04) and well-based RPPA (P = 0.04). VEGF quantification by well-based RPPA also demonstrated an association with nodal metastasis status (P = 0.05). In addition, the normalized VEGF value by well-based RPPA correlated (r = 0.283, P = 0.018). Furthermore, subgroup analysis by histologic type revealed that adenocarcinoma cases showed significant correlation (r = 0.315, P = 0.031) between well-based RPPA and IHC.
The well-based RPPA method is a high throughput and sensitive approach, is an excellent tool for quantification of marker proteins. Notably, this method may be helpful for more objective evaluation of protein expression in cancer patients.