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dc.contributor.authorSaxena, Vishal
dc.contributor.authorOrgill, Dennis P.
dc.contributor.authorKohane, Isaac
dc.date.accessioned2010-10-08T19:48:18Z
dc.date.available2010-10-08T19:48:18Z
dc.date.issued2007-11
dc.date.submitted2006-11
dc.identifier.issn1471-2164
dc.identifier.urihttp://hdl.handle.net/1721.1/58998
dc.description.abstractBackground: Wounds are increasingly important in our aging societies. Pathologies such as diabetes predispose patients to chronic wounds that can cause pain, infection, and amputation. The vacuum assisted closure device shows remarkable outcomes in wound healing. Its mechanism of action is unclear despite several hypotheses advanced. We previously hypothesized that micromechanical forces can heal wounds. To understand better the biological response of soft tissue to forces, rat ears in vivo were stretched and their gene expression patterns over time obtained. The absolute enrichment (AE) algorithm that obtains a combined up and down regulated picture of the expression analysis was implemented. Results: With the use of AE, the hypoxia gene set was the most important at a highly significant level. A co-expression network analysis showed that important co-regulated members of the hypoxia pathway include a glucose transporter (slc2a8), heme oxygenase, and nitric oxide synthase2 among others. Conclusion: It appears that the hypoxia pathway may be an important modulator of response of soft tissue to forces. This finding gives us insights not only into the underlying biology, but also into clinical interventions that could be designed to mimic within wounded tissue the effects of forces without all the negative effects that forces themselves create.en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/1471-2164-8-430en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleA set of genes previously implicated in the hypoxia response might be an important modulator in the rat ear tissue response to mechanical stretchen_US
dc.typeArticleen_US
dc.identifier.citationBMC Genomics. 2007 Nov 23;8(1):430en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorKohane, Isaac
dc.relation.journalBMC Genomicsen_US
dc.eprint.versionFinal published versionen_US
dc.identifier.pmid18034909
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2010-09-03T16:07:10Z
dc.language.rfc3066en
dc.rights.holderSaxena et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsSaxena, Vishal; Orgill, Dennis; Kohane, Isaacen
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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