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dc.contributor.authorTang, Chenkang
dc.contributor.authorShao, Ximing
dc.contributor.authorSun, Binbin
dc.contributor.authorHuang, Wenli
dc.contributor.authorZhao, Xiaojun
dc.date.accessioned2011-08-15T17:44:36Z
dc.date.available2011-08-15T17:44:36Z
dc.date.issued2009-05
dc.date.submitted2009-03
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/1721.1/65145
dc.description.abstractNanofiber scaffolds formed by self-assembling peptide RADA16-I have been used for the study of cell proliferation to mimic an extracellular matrix. In this study, we investigated the effect of RADA16-I on the growth of human leukemia cells in vitro and in nude mice. Self-assembly assessment showed that RADA16-I molecules have excellent self-assembling ability to form stable nanofibers. MTT assay displayed that RADA16-I has no cytotoxicity for leukemia cells and human umbilical vein endothelial cells (HUVECs) in vitro. However, RADA16-I inhibited the growth of K562 tumors in nude mice. Furthermore, we found RADA16-I inhibited vascular tube-formation by HUVECs in vitro. Our data suggested that nanofiber scaffolds formed by RADA16-I could change tumor microenvironments, and inhibit the growth of tumors. The study helps to encourage further design of self-assembling systems for cancer therapy.en_US
dc.description.sponsorshipChina. Ministry of Education (project 985)en_US
dc.language.isoen_US
dc.publisherMolecular Diversity Preservation Internationalen_US
dc.relation.isversionofhttp://dx.doi.org/10.3390/ijms10052136en_US
dc.rightsCreative Commons Attribution 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0en_US
dc.sourceMDPIen_US
dc.titleThe Effect of Self-Assembling Peptide RADA16-I on the Growth of Human Leukemia Cells in Vitro and in Nude Miceen_US
dc.typeArticleen_US
dc.identifier.citationTang, Chengkang et al. “The Effect of Self-Assembling Peptide RADA16-I on the Growth of Human Leukemia Cells in Vitro and in Nude Mice.” International Journal of Molecular Sciences 10.5 (2009) : 2136-2145. © 2009 MDPI Publishing.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Biomedical Engineeringen_US
dc.contributor.approverZhao, Xiaojun
dc.contributor.mitauthorZhao, Xiaojun
dc.relation.journalInternational Journal of Molecular Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsTang, Chengkang; Shao, Ximing; Sun, Binbin; Huang, Wenli; Zhao, Xiaojunen
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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