Microfluidic cytometric analysis of cancer cell transportability and invasiveness View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2015-11

AUTHORS

Zongbin Liu, Yeonju Lee, Joon hee Jang, Ying Li, Xin Han, Kenji Yokoi, Mauro Ferrari, Ledu Zhou, Lidong Qin

ABSTRACT

The extensive phenotypic and functional heterogeneity of cancer cells plays an important role in tumor progression and therapeutic resistance. Characterizing this heterogeneity and identifying invasive phenotype may provide possibility to improve chemotherapy treatment. By mimicking cancer cell perfusion through circulatory system in metastasis, we develop a unique microfluidic cytometry (MC) platform to separate cancer cells at high throughput, and further derive a physical parameter 'transportability' to characterize the ability to pass through micro-constrictions. The transportability is determined by cell stiffness and cell-surface frictional property, and can be used to probe tumor heterogeneity, discriminate more invasive phenotypes and correlate with biomarker expressions in breast cancer cells. Decreased cell stiffness and cell-surface frictional force leads to an increase in transportability and may be a feature of invasive cancer cells by promoting cell perfusion through narrow spaces in circulatory system. The MC-Chip provides a promising microfluidic platform for studying cell mechanics and transportability could be used as a novel marker for probing tumor heterogeneity and determining invasive phenotypes. More... »

PAGES

14272

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/srep14272

DOI

http://dx.doi.org/10.1038/srep14272

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1003484287

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/26404901


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