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dc.contributor.authorSnippert, Hugo J.
dc.contributor.authorSchepers, Arnout G.
dc.contributor.authorvan Es, Johan H.
dc.contributor.authorSimons, Benjamin D.
dc.contributor.authorClevers, Hans
dc.date.accessioned2024-11-05T20:00:12Z
dc.date.available2024-11-05T20:00:12Z
dc.date.issued2013-12-16
dc.identifier.urihttps://hdl.handle.net/1721.1/157497
dc.description.abstractThe concept of ‘field cancerization’ describes the clonal expansion of genetically altered, but morphologically normal cells that predisposes a tissue to cancer development. Here, we demonstrate that biased stem cell competition in the mouse small intestine can initiate the expansion of such clones. We quantitatively analyze how the activation of oncogenic K‐ras in individual Lgr5+ stem cells accelerates their cell division rate and creates a biased drift towards crypt clonality. K‐ras mutant crypts then clonally expand within the epithelium through enhanced crypt fission, which distributes the existing Paneth cell niche over the two new crypts. Thus, an unequal competition between wild‐type and mutant intestinal stem cells initiates a biased drift that leads to the clonal expansion of crypts carrying oncogenic mutations.en_US
dc.publisherNature Publishing Group UKen_US
dc.relation.isversionofhttps://doi.org/10.1002/embr.201337799en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Publishing Group UKen_US
dc.titleBiased competition between Lgr5 intestinal stem cells driven by oncogenic mutation induces clonal expansionen_US
dc.typeArticleen_US
dc.identifier.citationEMBO rep (2013) 15: 62 - 69en_US
dc.contributor.departmentHarvard-MIT Program in Health Sciences and Technologyen_US
dc.relation.journalEmbo Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2024-10-27T17:20:47Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.date.submission2024-10-27T17:20:47Z
mit.journal.volume15en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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