The BRG1 ATPase of human SWI/SNF chromatin remodeling enzymes as a driver of cancer
dc.contributor.author | Wu, Qiong | |
dc.contributor.author | Lian, Jane B. | |
dc.contributor.author | Stein, Janet L. | |
dc.contributor.author | Stein, Gary S. | |
dc.contributor.author | Nickerson, Jeffrey A. | |
dc.contributor.author | Imbalzano, Anthony N. | |
dc.date | 2022-08-11T08:10:13.000 | |
dc.date.accessioned | 2022-08-23T16:59:26Z | |
dc.date.available | 2022-08-23T16:59:26Z | |
dc.date.issued | 2017-06-01 | |
dc.date.submitted | 2017-07-20 | |
dc.identifier.citation | Epigenomics. 2017 Jun;9(6):919-931. doi: 10.2217/epi-2017-0034. Epub 2017 May 19. <a href="https://doi.org/10.2217/epi-2017-0034">Link to article on publisher's site</a> | |
dc.identifier.issn | 1750-192X (Linking) | |
dc.identifier.doi | 10.2217/epi-2017-0034 | |
dc.identifier.pmid | 28521512 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/43585 | |
dc.description.abstract | Mammalian SWI/SNF enzymes are ATP-dependent remodelers of chromatin structure. These multisubunit enzymes are heterogeneous in composition; there are two catalytic ATPase subunits, BRM and BRG1, that are mutually exclusive, and additional subunits are incorporated in a combinatorial manner. Recent findings indicate that approximately 20% of human cancers contain mutations in SWI/SNF enzyme subunits, leading to the conclusion that the enzyme subunits are critical tumor suppressors. However, overexpression of specific subunits without apparent mutation is emerging as an alternative mechanism by which cellular transformation may occur. Here we highlight recent evidence linking elevated expression of the BRG1 ATPase to tissue-specific cancers and work suggesting that inhibiting BRG1 may be an effective therapeutic strategy. | |
dc.language.iso | en_US | |
dc.relation | <a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28521512&dopt=Abstract">Link to Article in PubMed</a> | |
dc.relation.url | https://doi.org/10.2217/epi-2017-0034 | |
dc.rights | © Anthony N. Imbalzano. | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | ADAADi | |
dc.subject | BRG1 | |
dc.subject | BRM | |
dc.subject | PFI-3 | |
dc.subject | breast cancer | |
dc.subject | cancer metabolism | |
dc.subject | chromatin remodeling | |
dc.subject | drug transporters | |
dc.subject | mammalian SWI/SNF enzymes | |
dc.subject | Biochemistry, Biophysics, and Structural Biology | |
dc.subject | Cancer Biology | |
dc.subject | Cell Biology | |
dc.subject | Genetics and Genomics | |
dc.title | The BRG1 ATPase of human SWI/SNF chromatin remodeling enzymes as a driver of cancer | |
dc.type | Journal Article | |
dc.source.journaltitle | Epigenomics | |
dc.source.volume | 9 | |
dc.source.issue | 6 | |
dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1154&context=peds_pp&unstamped=1 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/peds_pp/155 | |
dc.identifier.contextkey | 10456093 | |
refterms.dateFOA | 2022-08-23T16:59:26Z | |
html.description.abstract | <p>Mammalian SWI/SNF enzymes are ATP-dependent remodelers of chromatin structure. These multisubunit enzymes are heterogeneous in composition; there are two catalytic ATPase subunits, BRM and BRG1, that are mutually exclusive, and additional subunits are incorporated in a combinatorial manner. Recent findings indicate that approximately 20% of human cancers contain mutations in SWI/SNF enzyme subunits, leading to the conclusion that the enzyme subunits are critical tumor suppressors. However, overexpression of specific subunits without apparent mutation is emerging as an alternative mechanism by which cellular transformation may occur. Here we highlight recent evidence linking elevated expression of the BRG1 ATPase to tissue-specific cancers and work suggesting that inhibiting BRG1 may be an effective therapeutic strategy.</p> | |
dc.identifier.submissionpath | peds_pp/155 | |
dc.contributor.department | Biochemistry and Molecular Pharmacology | |
dc.contributor.department | Pediatrics | |
dc.source.pages | 919-931 |