TY - JOUR
T1 - Adipose Cells Induce Escape from an Engineered Human Breast Microtumor Independently of their Obesity Status
AU - Dance, Yoseph W.
AU - Obenreder, Mackenzie C.
AU - Seibel, Alex J.
AU - Meshulam, Tova
AU - Ogony, Joshua W.
AU - Lahiri, Nikhil
AU - Pacheco-Spann, Laura
AU - Radisky, Derek C.
AU - Layne, Matthew D.
AU - Farmer, Stephen R.
AU - Nelson, Celeste M.
AU - Tien, Joe
N1 - Publisher Copyright:
© 2022, The Author(s) under exclusive licence to Biomedical Engineering Society.
PY - 2023/2
Y1 - 2023/2
N2 - Introduction: Obesity is associated with increased breast cancer incidence, recurrence, and mortality. Adipocytes and adipose-derived stem cells (ASCs), two resident cell types in adipose tissue, accelerate the early stages of breast cancer progression. It remains unclear whether obesity plays a role in the subsequent escape of malignant breast cancer cells into the local circulation. Methods: We engineered models of human breast tumors with adipose stroma that exhibited different obesity-specific alterations. We used these models to assess the invasion and escape of breast cancer cells into an empty, blind-ended cavity (as a mimic of a lymphatic vessel) for up to sixteen days. Results: Lean and obese donor-derived adipose stroma hastened escape to similar extents. Moreover, a hypertrophic adipose stroma did not affect the rate of adipose-induced escape. When admixed directly into the model tumors, lean and obese donor-derived ASCs hastened escape similarly. Conclusions: This study demonstrates that the presence of adipose cells, independently of the obesity status of the adipose tissue donor, hastens the escape of human breast cancer cells in multiple models of obesity-associated breast cancer.
AB - Introduction: Obesity is associated with increased breast cancer incidence, recurrence, and mortality. Adipocytes and adipose-derived stem cells (ASCs), two resident cell types in adipose tissue, accelerate the early stages of breast cancer progression. It remains unclear whether obesity plays a role in the subsequent escape of malignant breast cancer cells into the local circulation. Methods: We engineered models of human breast tumors with adipose stroma that exhibited different obesity-specific alterations. We used these models to assess the invasion and escape of breast cancer cells into an empty, blind-ended cavity (as a mimic of a lymphatic vessel) for up to sixteen days. Results: Lean and obese donor-derived adipose stroma hastened escape to similar extents. Moreover, a hypertrophic adipose stroma did not affect the rate of adipose-induced escape. When admixed directly into the model tumors, lean and obese donor-derived ASCs hastened escape similarly. Conclusions: This study demonstrates that the presence of adipose cells, independently of the obesity status of the adipose tissue donor, hastens the escape of human breast cancer cells in multiple models of obesity-associated breast cancer.
KW - Fat
KW - Hypertrophy
KW - Intravasation
KW - Microphysiological system
KW - Microvascular tissue engineering
KW - Triple-negative breast cancer
KW - Tumor engineering
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U2 - 10.1007/s12195-022-00750-y
DO - 10.1007/s12195-022-00750-y
M3 - Article
C2 - 36660589
AN - SCOPUS:85143582961
SN - 1865-5025
VL - 16
SP - 23
EP - 39
JO - Cellular and Molecular Bioengineering
JF - Cellular and Molecular Bioengineering
IS - 1
ER -