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dc.contributor.authorLam, Fred C
dc.contributor.authorKong, Yi Wen
dc.contributor.authorYaffe, Michael B
dc.date.accessioned2021-10-27T19:53:04Z
dc.date.available2021-10-27T19:53:04Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/133481
dc.description.abstract© 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. R-loops are intermediate structures of transcription that can accumulate when transcriptional elongation is blocked by inhibiting BRD4. In normal cells, R-loop persistence suppresses firing of adjacent replication origins. This control is lost in a subset of cancer cells, where BRD4 inhibition results in R-loop accumulation, leading to transcription-replication collisions and DNA double-strand breaks during S-phase, followed by cell death. This finding sheds new light on the mechanisms by which BRD4 inhibitors function as cancer therapies, and indicates that targeting other cellular events to cause R-loop accumulation may be useful for cancer treatment.
dc.language.isoen
dc.publisherInforma UK Limited
dc.relation.isversionof10.1080/23723556.2020.1848233
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs License
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceTaylor & Francis
dc.titleInducing DNA damage through R-loops to kill cancer cells
dc.typeArticle
dc.relation.journalMolecular and Cellular Oncology
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-08-04T15:48:55Z
dspace.orderedauthorsLam, FC; Kong, YW; Yaffe, MB
dspace.date.submission2021-08-04T15:48:56Z
mit.journal.volume8
mit.journal.issue1
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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