Abstract
Brain metastases are the most lethal complication of advanced cancer; therefore, it is critical to identify when a tumor has the potential to metastasize to the brain. There are currently no interventions that shed light on the potential of primary tumors to metastasize to the brain. We constructed and tested a platform to quantitatively profile the dynamic phenotypes of cancer cells from aggressive triple negative breast cancer cell lines and patient derived xenografts (PDXs), generated from a primary tumor and brain metastases from tumors of diverse organs of origin. Combining an advanced live cell imaging algorithm and artificial intelligence, we profile cancer cell extravasation within a microfluidic blood-brain niche (μBBN) chip, to detect the minute differences between cells with brain metastatic potential and those without with a PPV of 0.91 in the context of this study. The results show remarkably sharp and reproducible distinction between cells that do and those which do not metastasize inside of the device.
Original language | English |
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Pages (from-to) | 1162-1173 |
Number of pages | 12 |
Journal | Lab on a Chip |
Volume | 19 |
Issue number | 7 |
DOIs | |
Publication status | Published - Apr 7 2019 |
Bibliographical note
Funding Information:Work was supported by: NIH T32CA009676 (CRO, MA), the University of Michigan Rogel Cancer Center Nancy Newton Loeb Fund (MA), by NIH grants P30CA046592 (BL, SDM, MA, CRO), CA196018 (CRO, ST), AI116482 (CRO, ST), by the META-vivor Foundation (MA, SDM) and the Breast Cancer Research Foundation (CRO, SDM).
Publisher Copyright:
© 2019 The Royal Society of Chemistry.
ASJC Scopus Subject Areas
- Bioengineering
- Biochemistry
- General Chemistry
- Biomedical Engineering
PubMed: MeSH publication types
- Journal Article
- Research Support, N.I.H., Extramural