The interplay between
cancer cell physical characteristics
and
metastatic potential highlights the significance of cancer cell mechanobiology.
Using fluidic-based single-cell force spectroscopy (SCFS), quartz
crystal microbalance with dissipation (QCM-D), and a model of cells
with a spectrum of metastatic potential, we track the progression
of biomechanics across the metastatic states by measuring cell–substrate
and cell-to-cell adhesion forces, cell spring constant, cell height,
and cell viscoelasticity. Compared to highly metastatic cells, cells
in the lower spectrum of metastatic ability are found to be systematically
stiffer, less viscoelastic, and larger. These mechanical transformations
in cells within a cluster correlate with cells’ metastatic
potential but are significantly absent in single cells. Additionally,
the response to chemotherapy is found to be highly dependent on cell
viscoelastic properties in terms of both response time and magnitude.
Shifts in cell softness and elasticity might serve as mechanoadaptive
mechanisms during cancer cell metastasis, contributing to our understanding
of metastasis and the effectiveness of potential therapeutic interventions.