Format

Send to

Choose Destination
Mol Syst Biol. 2018 Aug 6;14(8):e8322. doi: 10.15252/msb.20188322.

Tumor-stroma interactions differentially alter drug sensitivity based on the origin of stromal cells.

Author information

1
Program in Systems Biology, Program in Molecular Medicine, Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, USA.
2
Department of Chemical Engineering, University of Massachusetts, Amherst, MA, USA.
3
Program in Systems Biology, Program in Molecular Medicine, Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, USA michael.lee@umassmed.edu.

Abstract

Due to tumor heterogeneity, most believe that effective treatments should be tailored to the features of an individual tumor or tumor subclass. It is still unclear, however, what information should be considered for optimal disease stratification, and most prior work focuses on tumor genomics. Here, we focus on the tumor microenvironment. Using a large-scale coculture assay optimized to measure drug-induced cell death, we identify tumor-stroma interactions that modulate drug sensitivity. Our data show that the chemo-insensitivity typically associated with aggressive subtypes of breast cancer is not observed if these cells are grown in 2D or 3D monoculture, but is manifested when these cells are cocultured with stromal cells, such as fibroblasts. Furthermore, we find that fibroblasts influence drug responses in two distinct and divergent manners, associated with the tissue from which the fibroblasts were harvested. These divergent phenotypes occur regardless of the drug tested and result from modulation of apoptotic priming within tumor cells. Our study highlights unexpected diversity in tumor-stroma interactions, and we reveal new principles that dictate how fibroblasts alter tumor drug responses.

KEYWORDS:

drug sensitivity; precision medicine; triple‐negative breast cancer; tumor microenvironment; tumor–stroma interaction

PMID:
30082272
PMCID:
PMC6078165

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center