Aging of breast tissue microenvironment has reported to form a fertile soil facilitating tumor progression. As tissue hemostasis evolves over the course of aging, developing models that enable the exploration of tumor progression in aging niche is important for understanding the disease, identifying crucial pathways, and finding control points that could be amenable to therapeutic intervention. Systematic inquiry of the aged breast tissue environment has been challenging and cost prohibitive, due to 1) lack of aged NORMAL breast tissue (an ideal control) for tissue microenvironment analysis and 2) the logistic barrier of lengthy aging process when using experimental mouse models. A fully characterized, tissue engineered breast model that faithfully recapitulates breast cancer development in an aging-mimicking tissue would be a novel platform for studying breast cancer progression, and would bring a new perspective to breast cancer research. Using a microfabricated tissue engineered model, we can explore what constitutes a permissive aging stromal environment by modulating variables such as matrix stiffness, matrix components, stromal cell density and organization, etc. The central goals of the proposed effort are to establish an Aging-mimicking Breast Tissue engineered (ABTe) that will be used to characterize the factors that contribute to the permissive environment in aging tissues, including the physical, chemical, and cellular cues, and to investigate whether therapeutic modulation can affect tumor progression in aging microenvironment. Specifically we aim to 1) Characterize biophysical properties and biochemical composition of extracellular matrices (ECM) of aged breast tissue; and 2) Build ABTe system and model ECM heterogeneity by tuning aging-related ECM factors including ECM stiffness, ECM composition, and stromal adipocytes spatial distribution, and then 3) test the clinical relevance and power of the developed ABTe by running chemoprevention trails for prevention of transition from Ductal Carcinoma In Situ (DCIS) to Invasive Ductal Carcinoma (IDC). To achieve these goals, we will combine our expertise of tissue engineering and breast cancer research. Once fully implemented and functionally validated, we expect our state-of-the-art tissue engineered ABTe cancer model to serve as the next-generation research platform for both basic and translational cancer research and high-throughput drug discovery. The tissue engineered ABTe will greatly facilitate research efforts in important, while traditionally less accessible, areas of cancer research and beyond.

Public Health Relevance

The goal of this study is to design and develop a fully characterized novel Aging-mimicking Breast Tissue engineered (ABTe) system as a disease model. With a fully integrative approach implementing human tissue analysis, state-of-art tissue engineering approaches and a comparative mouse study for physiological relevance, we propose a highly interdisciplinary project to reconstruct and validate ABTe at the molecular, cellular and physiological levels. The tissue engineered ABTe will greatly facilitate research efforts in important, while traditionally less accessible, areas of biomedical research, such as chemoprevention drug development and beyond.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB027660-02
Application #
9920718
Study Section
Cellular and Molecular Technologies Study Section (CMT)
Program Officer
Rampulla, David
Project Start
2019-05-01
Project End
2023-01-31
Budget Start
2020-02-01
Budget End
2021-01-31
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Notre Dame
Department
Engineering (All Types)
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
824910376
City
Notre Dame
State
IN
Country
United States
Zip Code
46556