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dc.contributor.authorKalchman, Johann
dc.contributor.authorFujioka, Shingo
dc.contributor.authorChung, Seok
dc.contributor.authorKikkawa, Yamato
dc.contributor.authorMitaka, Toshihiro
dc.contributor.authorTanishita, Kazuo
dc.contributor.authorSudo, Ryo
dc.contributor.authorKamm, Roger Dale
dc.date.accessioned2016-10-03T18:53:14Z
dc.date.available2016-10-03T18:53:14Z
dc.date.issued2012-12
dc.date.submitted2012-03
dc.identifier.issn1613-4982
dc.identifier.issn1613-4990
dc.identifier.urihttp://hdl.handle.net/1721.1/104639
dc.description.abstractMost anti-cancer drug screening assays are currently performed in two dimensions, on flat, rigid surfaces. However, there are increasing indications that three-dimensional (3D) platforms provide a more realistic setting to investigate accurate morphology, growth, and sensitivity of tumor cells to chemical factors. Moreover, interstitial flow plays a pivotal role in tumor growth. Here, we present a microfluidic 3D platform to investigate behaviors of tumor cells in flow conditions with anti-migratory compounds. Our results show that interstitial flow and its direction have significant impact on migration and growth of hepatocellular carcinoma cell lines such as HepG2 and HLE. In particular, HepG2/HLE cells tend to migrate against interstitial flow, and their growth increases in interstitial flow conditions regardless of the flow direction. Furthermore, this migratory activity of HepG2 cells is enhanced when they are co-cultured with human umbilical vein endothelial cells. We also found that migration activity of HepG2 cells attenuates under hypoxic conditions. In addition, the effect of Artemisinin, an anti-migratory compound, on HepG2 cells was quantitatively analyzed. The microfluidic 3D platform described here is useful to investigate more accurately the effect of anti-migratory drugs on tumor cells and the critical influence of interstitial flow than 2D culture models.en_US
dc.description.sponsorshipJapan Society for the Promotion of Science (22680037)en_US
dc.description.sponsorshipJapan Society for the Promotion of Science (G2212)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (R21CA140096)en_US
dc.description.sponsorshipJapan. Ministry of Education, Culture, Sports, Science and Technology (2009-00631)en_US
dc.description.sponsorshipJapan. Ministry of Education, Culture, Sports, Science and Technology (2012-0009565)en_US
dc.description.sponsorshipKorea (South). Ministry of Education & Human Resources Development (MOEHRD)en_US
dc.description.sponsorshipKorea (South). Ministry of Education & Human Resources Development (MOEHRD) (20124010203250)en_US
dc.publisherSpringer-Verlagen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s10404-012-1104-6en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceSpringer-Verlagen_US
dc.titleA three-dimensional microfluidic tumor cell migration assay to screen the effect of anti-migratory drugs and interstitial flowen_US
dc.typeArticleen_US
dc.identifier.citationKalchman, Johann, Shingo Fujioka, Seok Chung, Yamato Kikkawa, Toshihiro Mitaka, Roger D. Kamm, Kazuo Tanishita, and Ryo Sudo. “A Three-Dimensional Microfluidic Tumor Cell Migration Assay to Screen the Effect of Anti-Migratory Drugs and Interstitial Flow.” Microfluidics and Nanofluidics 14, no. 6 (December 4, 2012): 969–981.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.mitauthorKamm, Roger Dale
dc.relation.journalMicrofluidics and Nanofluidicsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2016-08-18T15:36:35Z
dc.language.rfc3066en
dc.rights.holderSpringer-Verlag Berlin Heidelberg
dspace.embargo.termsNen
dc.identifier.orcidhttps://orcid.org/0000-0002-7232-304X
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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