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dc.contributor.authorTape, CJ
dc.date.accessioned2017-02-01T12:31:09Z
dc.date.issued2017-02
dc.identifier.citationTrends in cancer, 2017, 3 (2), pp. 79 - 88
dc.identifier.issn2405-8033
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/403
dc.identifier.eissn2405-8025
dc.identifier.doi10.1016/j.trecan.2016.12.004
dc.description.abstractTissues contain multiple different cell types and can be considered to be heterocellular systems. Signaling between different cells allows tissues to achieve phenotypes that no cell type can achieve in isolation. Such emergent tissue-level phenotypes can be said to 'supervene upon' heterocellular signaling. It is proposed here that cancer is also an emergent phenotype that supervenes upon heterocellular signaling. Using colorectal cancer (CRC) as an example, I review how heterotypic cells differentially communicate to support emergent malignancy. Studying tumors as integrated heterocellular systems - rather than as solitary expansions of mutated cells - may reveal novel ways to treat cancer.
dc.formatPrint
dc.format.extent79 - 88
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectClone Cells
dc.subjectHumans
dc.subjectColorectal Neoplasms
dc.subjectCell Communication
dc.subjectSignal Transduction
dc.subjectCell Lineage
dc.subjectGenetic Heterogeneity
dc.titleThe Heterocellular Emergence of Colorectal Cancer.
dc.typeJournal Article
rioxxterms.versionofrecord10.1016/j.trecan.2016.12.004
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-02
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfTrends in cancer
pubs.issue2
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Oncogene
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Oncogene
pubs.publication-statusPublished
pubs.volume3
pubs.embargo.termsNot known
icr.researchteamOncogeneen_US
dc.contributor.icrauthorTape, Christopher


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