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dc.contributor.authorMansur, MB
dc.contributor.authorFord, AM
dc.contributor.authorEmerenciano, M
dc.date.accessioned2017-11-24T15:37:00Z
dc.date.issued2017-12-01
dc.identifier.citationBiochimica et biophysica acta. Reviews on cancer, 2017, 1868 (2), pp. 521 - 526
dc.identifier.issn0304-419X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/952
dc.identifier.eissn1879-2561
dc.identifier.doi10.1016/j.bbcan.2017.10.005
dc.description.abstractChildhood acute lymphoblastic leukaemia (ALL) with MLL rearrangement (MLL-r) is an aggressive disease still associated with a high mortality rate. Recent investigations have identified co-operating mutations in the RAS pathway and although the functional consequences of these mutations are not yet fully understood, aberrant regulation of RAS pathway signalling at both transcriptional and protein levels is observed. Studies investigating the efficacy of specific inhibitors of this pathway, e.g. MEK-inhibitors, have also achieved encouraging results. In this context, this mini-review summarizes the available data surrounding MLL-r infant ALL with RAS mutation in relation to other well-known features of this intriguing disease.
dc.formatPrint-Electronic
dc.format.extent521 - 526
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER
dc.rights.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
dc.subjectHumans
dc.subjectHistone-Lysine N-Methyltransferase
dc.subjectMitogen-Activated Protein Kinase Kinases
dc.subjectGene Rearrangement
dc.subjectMutation
dc.subjectGenes, ras
dc.subjectMyeloid-Lymphoid Leukemia Protein
dc.subjectfms-Like Tyrosine Kinase 3
dc.subjectPrecursor Cell Lymphoblastic Leukemia-Lymphoma
dc.titleThe role of RAS mutations in MLL-rearranged leukaemia: A path to intervention?
dc.typeJournal Article
dcterms.dateAccepted2017-10-18
rioxxterms.versionofrecord10.1016/j.bbcan.2017.10.005
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
rioxxterms.licenseref.startdate2017-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBiochimica et biophysica acta. Reviews on cancer
pubs.issue2
pubs.notesNo embargo
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/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Biology of Childhood Leukaemia
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/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Biology of Childhood Leukaemia
pubs.publication-statusPublished
pubs.volume1868
pubs.embargo.termsNo embargo
icr.researchteamBiology of Childhood Leukaemia
dc.contributor.icrauthorFord, Anthony


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