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NPPB is a novel candidate biomarker expressed by cancer‐associated fibroblasts in epithelial ovarian cancer
Author(s) -
Lawrenson Kate,
Grun Barbara,
Lee Nathan,
MhawechFauceglia Paulette,
Kan Jenny,
Swenson Steve,
Lin Yvonne G.,
Pejovic Tanja,
Millstein Joshua,
Gayther Simon A.
Publication year - 2014
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.29092
Subject(s) - ovarian cancer , cancer associated fibroblasts , cancer research , stroma , carcinogenesis , biology , cancer , cancer cell , mesenchymal stem cell , pathology , tumor microenvironment , medicine , immunology , immunohistochemistry , tumor cells , genetics
Most solid tumors contain cancer‐associated fibroblasts (CAFs) that support tumorigenesis and malignant progression. However, the cellular origins of CAFs in epithelial ovarian cancers (EOCs) remain poorly understood, and their utility as a source of clinical biomarkers for cancer diagnosis has not been explored in great depth. Here, we report establishing in vitro and in vivo models of CAFs in ovarian cancer development. Normal ovarian fibroblasts and mesenchymal stem cells cultured in the presence of EOC cells acquired a CAF‐like phenotype, and promoted EOC cell migration in vitro . CAFs also promoted ovarian cancer growth in vivo in both subcutaneous and intraperitoneal murine xenograft assays. Molecular profiling of CAFs identified gene expression signatures that were highly enriched for extracellular and secreted proteins. We identified novel candidate CAF‐specific biomarkers for ovarian cancer including NPPB, which was expressed in the stroma of 60% primary ovarian cancer tissues ( n  = 145) but not in the stroma of normal ovaries ( n  = 4). NPPB is a secreted protein that was also elevated in the blood of 50% of women with ovarian cancer ( n  = 8). Taken together, these data suggest that the tumor stroma is a novel source of biomarkers, including NPPB, that may be of clinical utility for detection of EOC.

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