학술논문

Transient external force induces phenotypic reversion of malignant epithelial structures via nitric oxide signaling.
Document Type
article
Source
Subject
Breast
Cell Line
Cell Line
Tumor
Extracellular Matrix
Epithelial Cells
Humans
Breast Neoplasms
Nitric Oxide
Laminin
Microscopy
Confocal
Signal Transduction
Stress
Mechanical
Time-Lapse Imaging
Acinar Cells
breast cancer
breast epithelial cells
cancer biology
cell biology
human
malignancy
mechanobiology
phenotypic reversion
Cancer
Breast Cancer
Biochemistry and Cell Biology
Language
Abstract
Non-malignant breast epithelial cells cultured in three-dimensional laminin-rich extracellular matrix (lrECM) form well organized, growth-arrested acini, whereas malignant cells form continuously growing disorganized structures. While the mechanical properties of the microenvironment have been shown to contribute to formation of tissue-specific architecture, how transient external force influences this behavior remains largely unexplored. Here, we show that brief transient compression applied to single malignant breast cells in lrECM stimulated them to form acinar-like structures, a phenomenon we term 'mechanical reversion.' This is analogous to previously described phenotypic 'reversion' using biochemical inhibitors of oncogenic pathways. Compression stimulated nitric oxide production by malignant cells. Inhibition of nitric oxide production blocked mechanical reversion. Compression also restored coherent rotation in malignant cells, a behavior that is essential for acinus formation. We propose that external forces applied to single malignant cells restore cell-lrECM engagement and signaling lost in malignancy, allowing them to reestablish normal-like tissue architecture.