TY - JOUR
T1 - Use of reverse phase protein microarrays and reference standard development for molecular network analysis of metastatic ovarian carcinoma
AU - Sheehan, Katherine M.
AU - Calvert, Valerie S.
AU - Kay, Elaine W.
AU - Lu, Yiling
AU - Fishman, David
AU - Espina, Virginia
AU - Aquino, Joy
AU - Speer, Runa
AU - Araujo, Robyn
AU - Mills, Gordon B.
AU - Liotta, Lance A.
AU - Petricoin, Emanuel F.
AU - Wulfkuhle, Julia D.
PY - 2005/4
Y1 - 2005/4
N2 - Cancer can be defined as a deregulation or hyperactivity in the ongoing network of intracellular and extracellular signaling events. Reverse phase protein microarray technology may offer a new opportunity to measure and profile these signaling pathways, providing data on post-translational phosphorylation events not obtainable by gene microarray analysis. Treatment of ovarian epithelial carcinoma almost always takes place in a metastatic setting since unfortunately the disease is often not detected until later stages. Thus, in addition to elucidation of the molecular network within a tumor specimen, critical questions are to what extent do signaling changes occur upon metastasis and are there common pathway elements that arise in the metastatic microenvironment. For individualized combinatorial therapy, ideal therapeutic selection based on proteomic mapping of phosphorylation end points may require evaluation of the patient's metastatic tissue. Extending these findings to the bedside will require the development of optimized protocols and reference standards. We have developed a reference standard based on a mixture of phosphorylated peptides to begin to address this challenge.
AB - Cancer can be defined as a deregulation or hyperactivity in the ongoing network of intracellular and extracellular signaling events. Reverse phase protein microarray technology may offer a new opportunity to measure and profile these signaling pathways, providing data on post-translational phosphorylation events not obtainable by gene microarray analysis. Treatment of ovarian epithelial carcinoma almost always takes place in a metastatic setting since unfortunately the disease is often not detected until later stages. Thus, in addition to elucidation of the molecular network within a tumor specimen, critical questions are to what extent do signaling changes occur upon metastasis and are there common pathway elements that arise in the metastatic microenvironment. For individualized combinatorial therapy, ideal therapeutic selection based on proteomic mapping of phosphorylation end points may require evaluation of the patient's metastatic tissue. Extending these findings to the bedside will require the development of optimized protocols and reference standards. We have developed a reference standard based on a mixture of phosphorylated peptides to begin to address this challenge.
UR - http://www.scopus.com/inward/record.url?scp=17844377553&partnerID=8YFLogxK
U2 - 10.1074/mcp.T500003-MCP200
DO - 10.1074/mcp.T500003-MCP200
M3 - Article
C2 - 15671044
AN - SCOPUS:17844377553
SN - 1535-9476
VL - 4
SP - 346
EP - 355
JO - Molecular and Cellular Proteomics
JF - Molecular and Cellular Proteomics
IS - 4
ER -