Myofibroblast Development in Breast Cancer

Malignant transformation of the breast and other organs is associated with dramatic changes in the microenvironment surrounding neoplastic cells, including a reactive fibrotic stroma characterized by increased production of inflammatory cytokines, excessive accumulation of extracellular matrix (ECM), and an increase in tissue stiffness. Contractile myofibroblasts are key mediators of the biochemical and biophysical properties of the fibrotic tumor microenvironment.

In addition, the transdifferentiation of myofibroblasts from tissue cells and their subsequent activation is controlled by a combination of soluble factors and contractile tension. The increased tissue stiffness associated with fibrosis may thereby generate a positive feedback loop to facilitate tumor progression and metastatic invasion.

Delineating the microenvironmental effects and effectors requires sophisticated, tractable model systems.

Our lab is developing an experimental model to define how alterations of the biochemical and biophysical cellular microenvironment can stimulate myofibroblast development and activation, and how formation and activation of myofibroblasts in tissue structures affects progression to malignancy.

We're using cell culture and animal studies to determine the biochemical and biomechanical requirements of the substratum microenvironment for the transdifferentiation process. We're also using a novel 3D microlithography-based organotypic culture system of the mammary epithelial ductal network to determine how myofibroblast transdifferentiation affects the microenvironment of the duct at the biochemical, mechanical and cell population levels.

Given that the presence of fibrotic foci in breast tumors correlates with metastasis and negative prognosis and might hinder the efficacy of tumor therapies, the new physiologically relevant models developed in our work may have a significant impact on the discovery and evaluation of novel therapeutic targets to combat fibrosis genesis and tumor progression.