4.7 Article

Expression patterns of bone morphogenetic protein antagonists in colorectal cancer desmoplastic invasion fronts

Journal

MOLECULAR ONCOLOGY
Volume 8, Issue 7, Pages 1240-1252

Publisher

WILEY
DOI: 10.1016/j.molonc.2014.04.004

Keywords

Bone morphogenetic; protein antagonists; Gremlin-1; Follistatin; High-temperature requirement-A3; Tumor budding; Cancer-associated fibroblasts; Colorectal cancer

Categories

Funding

  1. University Health Network and Mount Sinai Hospital, Toronto, ON, Canada

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Bone morphogenetic proteins (BMPs) are a group of growth factors with dual functions in cancer development and progression. Recently, certain tumor-promoting roles have been identified for selected antagonists/inhibitors (BMPIs) of this developmental pathway. A recent focus on the implication of BMP in colorectal cancer progression has emerged, mainly due to the presence of inactivating mutations in several members of the canonical signaling cascade. However, the detailed expression profiles of BMPIs remain largely unknown. Based on our previous work, whereby three specific BMPIs, gremlin-1 (GREM1), high-temperature requirement A3 (HTRA3) and follistatin (FST) were collectively overexpressed in desmoplastic cocultures of colorectal cancer (CRC), here, we undertook an immunohistochemical approach to describe the patterns of their expression in CRC patients. Two major characteristics described the BMPI expression signature: First, the synchronous and coordinated stromal and epithelial overexpression of individual BMPIs in desmoplastic lesions, which demonstrated that all three of them contribute to increasing levels of BMP antagonism in such areas. Second, the presence of microenvironmental polarity in the BMPI pattern of expression, which was indicated through the preferential expression of HTRA3 in the stromal, and the parallel FST/GREM1 expression in the epithelial component of the investigated sections. In addition, expression of HTRA3 in the epithelial compartment of the tumors demonstrated a significant predictive power to discriminate between tumor-budding-bearing and tumor-budding-free desmoplastic microenvironments. Together, these findings contribute to the understanding of signaling dynamics of BMP antagonism in the colorectal cancer desmoplastic invasion front. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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