4.7 Article

Rapid multilayer microfabrication for modeling organotropic metastasis in breast cancer

Journal

BIOFABRICATION
Volume 13, Issue 1, Pages -

Publisher

IOP PUBLISHING LTD
DOI: 10.1088/1758-5090/abbd28

Keywords

breast cancer; TNBC; tumor-on-a-chip; multilayer; extravasation; engineered vessels; organotropic metastasis

Funding

  1. Cornell University Start-up funds
  2. Nancy and Peter Meinig Family Investigator funds
  3. National Science Foundation [NNCI-1542081]

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Understanding the interaction between TNBC and blood vasculatures is crucial in studying and treating TNBC metastasis, particularly in the process of TNBC extravasation from blood vessels to determine the final site of metastasis. Modeling studies have shown that bone and lungs are common sites of breast cancer metastasis, and organ-specific parenchymal cells play a key role in the selective extravasation of TNBC cells in bone and lung microenvironments.
Triple-negative breast cancer (TNBC) is one of the most insidious forms of breast cancer with high rates of metastasis, resulting in major mortalities in breast cancer patients. To better understand and treat TNBC metastasis, investigation of TNBC interactions with blood vasculatures is crucial. Among multiple metastatic processes, a step of TNBC exit from the blood vessels ('extravasation') in the pre-metastatic organs determines the final site of the metastasis. Here, we present a rapid multilayer microfabrication method of transferring a three-dimensional (3D) overhang pattern to a substrate with a sacrificial layer to reconstitute a 3D blood vessel surrounded by the extracellular matrix containing organ-specific parenchymal cells. Bones and lungs are the most common sites of breast cancer metastasis. We modeled organotropic bone and lung metastasis in TNBC by introducing subpopulations of TNBC metastases into a vessel lumen surrounded by osteoblasts, bone marrow derived mesenchymal stem cells, and lung fibroblasts. We found that bone-like microenviroment with osteoblasts and mesenchymal stem cells promoted extravasation of the bone-tropic TNBC cells, whereas the lung-like microenviroment promoted extravasation of the lung-tropic TNBC cells. Given that these organ-specific parenchymal cells do not impact vascular permeability, our results suggest that the parenchymal cells dictate selective extravasation of the bone-tropic or lung-tropic TNBC cells in our system.

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