Pore Shape Defines Paths of Metastatic Cell Migration

Brenda J. Green, Magdalini Panagiotakopoulou, Francesca Michela Pramotton, Georgios Stefopoulos, Shana O. Kelley, Dimos Poulikakos*, Aldo Ferrari

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Invasion of dense tissues by cancer cells involves the interplay between the penetration resistance offered by interstitial pores and the deformability of cells. Metastatic cancer cells find optimal paths of minimal resistance through an adaptive path-finding process, which leads to successful dissemination. The physical limit of nuclear deformation is related to the minimal cross section of pores that can be successfully penetrated. However, this single biophysical parameter does not fully describe the architectural complexity of tissues featuring pores of variable area and shape. Here, employing laser nanolithography, we fabricate pore microenvironment models with well-controlled pore shapes, through which human breast cells (MCF10A) and their metastatic offspring (MCF10CA1a.cl1) could pervade. In these experimental settings, we demonstrate that the actual pore shape, and not only the cross section, is a major and independent determinant of cancer penetration efficiency. In complex architectures containing pores demanding large deformations from invading cells, tall and narrow rectangular openings facilitate cancer migration. In addition, we highlight the characteristic traits of the explorative behavior enabling metastatic cells to identify and select such pore shapes in a complex multishape pore environment, pinpointing paths of least resistance to invasion.

Original languageEnglish (US)
Pages (from-to)2140-2147
Number of pages8
JournalNano letters
Volume18
Issue number3
DOIs
StatePublished - Mar 14 2018

Funding

This work was part of the project “Novel Microengineered Platform for the Study of Interstitial Cell Migration” (Project 200021-146898) supported by the Swiss National Science Foundation (SNSF). F.M.P. was supported by funding from the ETH-grant ETH-07 17-1. We also thank the Natural Sciences and Engineering Council of Canada for the foreign supplement award, as well as Dr. Costanza Giampietro for her useful insights on protein expression of cancer cells.

ASJC Scopus subject areas

  • General Chemistry
  • Condensed Matter Physics
  • Mechanical Engineering
  • Bioengineering
  • General Materials Science

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