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PillarX: A Microfluidic Device to Profile Circulating Tumor Cell Clusters Based on Geometry, Deformability, and Epithelial State.
Green, Brenda J; Marazzini, Margherita; Hershey, Ben; Fardin, Amir; Li, Qingsen; Wang, Zongjie; Giangreco, Giovanni; Pisati, Federica; Marchesi, Stefano; Disanza, Andrea; Frittoli, Emanuela; Martini, Emanuele; Magni, Serena; Beznoussenko, Galina V; Vernieri, Claudio; Lobefaro, Riccardo; Parazzoli, Dario; Maiuri, Paolo; Havas, Kristina; Labib, Mahmoud; Sigismund, Sara; Fiore, Pier Paolo Di; Gunby, Rosalind H; Kelley, Shana O; Scita, Giorgio.
Afiliação
  • Green BJ; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Marazzini M; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Hershey B; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Fardin A; IEO, Istituto Europeo di Oncologia IRCCS, Via Ripamonti 435, Milan, 20141, Italy.
  • Li Q; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Wang Z; Institute for Biomaterials and Biomedical Engineering, University of Toronto, 144 College St, Toronto, Ontario, M5S 3M2, Canada.
  • Giangreco G; IEO, Istituto Europeo di Oncologia IRCCS, Via Ripamonti 435, Milan, 20141, Italy.
  • Pisati F; Tumour Cell Biology Laboratory, The Francis Crick Institute, 1 Midland Rd, London, NW1 1AT, UK.
  • Marchesi S; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Disanza A; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Frittoli E; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Martini E; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Magni S; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Beznoussenko GV; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Vernieri C; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Lobefaro R; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Parazzoli D; Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian 1, Milan, 20133, Italy.
  • Maiuri P; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Havas K; Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian 1, Milan, 20133, Italy.
  • Labib M; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Sigismund S; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Fiore PPD; IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.
  • Gunby RH; Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, IL, 60208, USA.
  • Kelley SO; IEO, Istituto Europeo di Oncologia IRCCS, Via Ripamonti 435, Milan, 20141, Italy.
  • Scita G; Department of Oncology and Haemato-Oncology, Università degli Studi di Milano, Via Festa del Perdono, 7, Milan, 20122, Italy.
Small ; 18(17): e2106097, 2022 04.
Article em En | MEDLINE | ID: mdl-35344274
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Células Neoplásicas Circulantes Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Small Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Células Neoplásicas Circulantes Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Revista: Small Assunto da revista: ENGENHARIA BIOMEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália