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Science1 publisherNot yet confirmed elsewhere3 min readPublished

Randomly placed pillars on a chip make tumour cell clusters break apart more often

ISTA and Crick researchers found tumour cell clusters split more often among randomly placed pillars than in an even 9-micrometre grid. The chip lets metastasis research test how tissue geometry around a tumour, apart from its genetics, can push cells to break away.

The Scientist · Science desk

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What happened

  • The disordered forests were made by shifting each pillar of the square lattice away from its position by a random angle and distance.
  • Among disordered pillars the cells' advancing edge roughened into finger-like protrusions, and cells were more likely to break away from the tips.
  • A simulation treating each cell as a bead attracted to its neighbours also showed more detachment in disordered geometry than in ordered geometry.

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Why it matters

  • capability Because the disorder is defined in software and made by lithography, labs can vary the surroundings of the same cells and measure detachment, testing environment separately from genetics.
  • constraint Anything past eight days rests on the bead simulation, so long-run claims about invasion from this work are model predictions until a longer-lived experiment checks them.
  • precedent If Sixt's follow-up finds that detaching in disorder leads to epigenetic and then genetic change, the environment becomes a candidate cause of malignancy as well as a route for spread.

The experiment turns on one variable. Cancer cells were placed at the centre of a pillar forest and tracked with fluorescence imaging and light microscopy for up to eight days [7]. In some designs the pillars sat on a square grid, repeating every 18 micrometres from centre to centre [16]. In the others, each pillar was shifted off that grid by a random angle and distance [4]. The pillars stand in for the tissue fibres that invading cells have to squeeze between [3].

Building the disorder took new tools. "There were no suitable tools for designing mathematically defined disorder," said Saren Tasciyan, who designed the devices during his PhD in Michael Sixt's group at ISTA [6]. He wrote software to define the patterns and turn them into designs manufactured with standard semiconductor lithography [6].

The clusters were more likely to break apart in the disordered forests than on the regular grid [8]. In those conditions, Sixt said, "we found that the first cells detach, exactly as happens in a cancer metastasis" [9]. The pillars roughened the advancing edge of the cluster into finger-like protrusions, and cells were more likely to leave from the tips [10]. "When the cell interface moves through this landscape the effects accumulate over time," Sixt said [11].

The Physics World account does not say how much more often the clusters split, or which cancer cells were used. The full study appeared in Science Advances [5].

Cells on the chip lasted eight days, so Edouard Hannezo's group at ISTA simulated the process over longer periods than the cells could survive [1] [12]. "Each cell was modelled as a bead that moves through an environment," said Zuzana Dunajová, the Hannezo group postdoc who built the model [13]. The beads attract one another and move through geometries that mimic the devices [13]. I think this is the most informative part of the work. As described, the model has cohesion and movement and nothing about genes, so whatever detachment it shows comes from geometry [17]. It still shed beads more often among disordered pillars: "the beads detached from the collective more often in the disordered environment compared to the ordered," Dunajová said [14].

She went further. "The roughness of the cancer-cell invasion actually follows the same kind of universal behaviour as we see in other systems, such as combustion of paper, spreading of fires or drying coffee drops," she said [18]. The claim concerns the statistics of a moving front. Physics World did not report the measurements behind it.

The chip cannot show whether a tumour in a body behaves the same way. The local environment that governs detachment includes blood vessels, immune cells and signalling molecules as well as connective tissue [2]. The chip isolates one item on that list, the geometry of the fibres, with pillars standing in for them [3].

What to watch

  • Whether the Science Advances paper's effect size, and the cell line it used, hold up when other groups run the same disordered geometries.
  • Sixt's follow-up on whether cells that detach in disordered forests go on to show epigenetic and then genetic changes.
  • Quantitative tests of whether the invasion front's roughness matches the universal behaviour Dunajová compares to burning paper and spreading fires.

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  1. [1]

    Researchers led by Michael Sixt (Cellular Morphodynamics Group) and Edouard Hannezo (Physical Principles in Biological Systems Group), both at the Institute of Science and Technology Austria (ISTA), with scientists from the Francis Crick Institute, built a microfluidic chip experiment and computer simulation showing that heterogeneity around a tumour can drive metastasis.

    ReportedSupportedView cited source
  2. [2]

    Cancers spread when individual cells detach from the tumour cell collective and invade healthy tissue; whether detachment occurs depends on both genetics and the local microenvironment, including blood vessels, immune cells, signalling molecules and connective tissue.

    ReportedSupportedView cited source
  3. [3]

    To replicate cancer cells squeezing through pores between the fibres of tissues they invade, the researchers created forests of pillars mounted on microfluidic devices.

    ReportedSupportedView cited source

Sources

1 independent publisher whose own reporting we read for this story.

  1. physicsworld.com

    1 article · October 8, 2026

    Disordered environments around tumour cells can promote cancer spread

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