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PillarX: A Microfluidic Device to Profile Circulating Tumor Cell Clusters Based on Geometry, Deformability, and Epithelial State

Authors :
Brenda J. Green
Margherita Marazzini
Ben Hershey
Amir Fardin
Qingsen Li
Zongjie Wang
Giovanni Giangreco
Federica Pisati
Stefano Marchesi
Andrea Disanza
Emanuela Frittoli
Emanuele Martini
Serena Magni
Galina V. Beznoussenko
Claudio Vernieri
Riccardo Lobefaro
Dario Parazzoli
Paolo Maiuri
Kristina Havas
Mahmoud Labib
Sara Sigismund
Pier Paolo Di Fiore
Rosalind H. Gunby
Shana O. Kelley
Giorgio Scita
Green, Bj
Marazzini, M
Hershey, B
Fardin, A
Li, Q
Wang, Z
Giangreco, G
Pisati, F
Marchesi, S
Disanza, A
Frittoli, E
Martini, E
Magni, S
Beznoussenko, Gv
Vernieri, C
Lobefaro, R
Parazzoli, D
Maiuri, P
Havas, K
Labib, M
Sigismund, S
Fiore, Ppd
Gunby, Rh
Kelley, So
Scita, G.
Publication Year :
2022

Abstract

Circulating tumor cell (CTC) clusters are associated with increased metastatic potential and worse patient prognosis, but are rare, difficult to count, and poorly characterized biophysically. The PillarX device described here is a bimodular microfluidic device (Pillar-device and an X-magnetic device) to profile single CTCs and clusters from whole blood based on their size, deformability, and epithelial marker expression. Larger, less deformable clusters and large single cells are captured in the Pillar-device and sorted according to pillar gap sizes. Smaller, deformable clusters and single cells are subsequently captured in the X-device and separated based on epithelial marker expression using functionalized magnetic nanoparticles. Clusters of established and primary breast cancer cells with variable degrees of cohesion driven by different cell-cell adhesion protein expression are profiled in the device. Cohesive clusters exhibit a lower deformability as they travel through the pillar array, relative to less cohesive clusters, and have greater collective invasive behavior. The ability of the PillarX device to capture clusters is validated in mouse models and patients of metastatic breast cancer. Thus, this device effectively enumerates and profiles CTC clusters based on their unique geometrical, physical, and biochemical properties, and could form the basis of a novel prognostic clinical tool.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....2318fd58a68238b3bd0604f6facc47c9