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Cho, Yoon-Kyoung
FRUITS Lab.
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dc.citation.endPage 4185 -
dc.citation.number 24 -
dc.citation.startPage 4171 -
dc.citation.title LAB ON A CHIP -
dc.citation.volume 17 -
dc.contributor.author Um, Eujin -
dc.contributor.author Oh, Jung Min -
dc.contributor.author Granick, Steve -
dc.contributor.author Cho, Yoon-Kyoung -
dc.date.accessioned 2023-12-21T21:20:49Z -
dc.date.available 2023-12-21T21:20:49Z -
dc.date.created 2017-12-29 -
dc.date.issued 2017-12 -
dc.description.abstract Recent advances in microengineered cell migration platforms are discussed critically with a focus on how cell migration is influenced by engineered tumor microenvironments, the medical relevance being to understand how tumor microenvironments may promote or suppress the progression of cancer. We first introduce key findings in cancer cell migration under the influence of the physical environment, which is systematically controlled by microengineering technology, followed by multi-cues of physico-chemical factors, which represent the complexity of the tumor environment. Recognizing that cancer cells constantly communicate not only with each other but also with tumor-associated cells such as vascular, fibroblast, and immune cells, and also with non-cellular components, it follows that cell motility in tumor microenvironments, especially metastasis via the invasion of cancer cells into the extracellular matrix and other tissues, is closely related to the malignancy of cancer-related mortality. Medical relevance of forefront research realized in microfabricated devices, such as single cell sorting based on the analysis of cell migration behavior, may assist personalized theragnostics based on the cell migration phenotype. Furthermore, we urge development of theory and numerical understanding of single or collective cell migration in microengineered platforms to gain new insights in cancer metastasis and in therapeutic strategies. -
dc.identifier.bibliographicCitation LAB ON A CHIP, v.17, no.24, pp.4171 - 4185 -
dc.identifier.doi 10.1039/c7lc00555e -
dc.identifier.issn 1473-0197 -
dc.identifier.scopusid 2-s2.0-85037612880 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/23226 -
dc.identifier.url http://pubs.rsc.org/en/Content/ArticleLanding/2017/LC/C7LC00555E#!divAbstract -
dc.identifier.wosid 000417107500001 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRY -
dc.title Cell migration in microengineered tumor environments -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Biochemical Research Methods; Chemistry, Multidisciplinary; Chemistry, Analytical; Nanoscience & Nanotechnology -
dc.relation.journalResearchArea Biochemistry & Molecular Biology; Chemistry; Science & Technology - Other Topics -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus MICROFLUIDIC PLATFORM -
dc.subject.keywordPlus SHEAR-STRESS -
dc.subject.keywordPlus INTERSTITIAL FLOW -
dc.subject.keywordPlus MATRIX STIFFNESS -
dc.subject.keywordPlus COCULTURE SYSTEM -
dc.subject.keywordPlus BREAST-CANCER -
dc.subject.keywordPlus IMMUNE CELLS -
dc.subject.keywordPlus EPITHELIAL-MESENCHYMAL TRANSITION -
dc.subject.keywordPlus CANCER-ASSOCIATED FIBROBLASTS -
dc.subject.keywordPlus ENDOTHELIAL BARRIER FUNCTION -

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