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dc.contributor.authorWu, Qiong
dc.contributor.authorMadany, Pasil A.
dc.contributor.authorAkech, Jacqueline
dc.contributor.authorDobson, Jason
dc.contributor.authorDouthwright, Stephen
dc.contributor.authorBrowne, Gillian
dc.contributor.authorColby, Jennifer L.
dc.contributor.authorWinter, Georg E.
dc.contributor.authorBradner, James E.
dc.contributor.authorPratap, Jitesh
dc.contributor.authorSluder, Greenfield
dc.contributor.authorBhargava, Rohit
dc.contributor.authorChiosea, Simion I.
dc.contributor.authorVan Wijnen, Andre J.
dc.contributor.authorStein, Janet L.
dc.contributor.authorStein, Gary S.
dc.contributor.authorLian, Jane B.
dc.contributor.authorNickerson, Jeffrey A.
dc.contributor.authorImbalzano, Anthony N.
dc.date2022-08-11T08:08:03.000
dc.date.accessioned2022-08-23T15:40:44Z
dc.date.available2022-08-23T15:40:44Z
dc.date.issued2015-11-01
dc.date.submitted2015-10-13
dc.identifier.citationJ Cell Physiol. 2015 Nov;230(11):2683-94. doi: 10.1002/jcp.24991. <a href="http://dx.doi.org/10.1002/jcp.24991">Link to article on publisher's site</a>
dc.identifier.issn0021-9541 (Linking)
dc.identifier.doi10.1002/jcp.24991
dc.identifier.pmid25808524
dc.identifier.urihttp://hdl.handle.net/20.500.14038/26470
dc.description.abstractThe Brahma (BRM) and Brahma-related Gene 1 (BRG1) ATPases are highly conserved homologs that catalyze the chromatin remodeling functions of the multi-subunit human SWI/SNF chromatin remodeling enzymes in a mutually exclusive manner. SWI/SNF enzyme subunits are mutated or missing in many cancer types, but are overexpressed without apparent mutation in other cancers. Here, we report that both BRG1 and BRM are overexpressed in most primary breast cancers independent of the tumor's receptor status. Knockdown of either ATPase in a triple negative breast cancer cell line reduced tumor formation in vivo and cell proliferation in vitro. Fewer cells in S phase and an extended cell cycle progression time were observed without any indication of apoptosis, senescence, or alterations in migration or attachment properties. Combined knockdown of BRM and BRG1 showed additive effects in the reduction of cell proliferation and time required for completion of cell cycle, suggesting that these enzymes promote cell cycle progression through independent mechanisms. Knockout of BRG1 or BRM using CRISPR/Cas9 technology resulted in the loss of viability, consistent with a requirement for both enzymes in triple negative breast cancer cells.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=25808524&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1002/jcp.24991
dc.subjectCancer Biology
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.titleThe SWI/SNF ATPases Are Required for Triple Negative Breast Cancer Cell Proliferation
dc.typeJournal Article
dc.source.journaltitleJournal of cellular physiology
dc.source.volume230
dc.source.issue11
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/cellbiology_pp/155
dc.identifier.contextkey7709821
html.description.abstract<p>The Brahma (BRM) and Brahma-related Gene 1 (BRG1) ATPases are highly conserved homologs that catalyze the chromatin remodeling functions of the multi-subunit human SWI/SNF chromatin remodeling enzymes in a mutually exclusive manner. SWI/SNF enzyme subunits are mutated or missing in many cancer types, but are overexpressed without apparent mutation in other cancers. Here, we report that both BRG1 and BRM are overexpressed in most primary breast cancers independent of the tumor's receptor status. Knockdown of either ATPase in a triple negative breast cancer cell line reduced tumor formation in vivo and cell proliferation in vitro. Fewer cells in S phase and an extended cell cycle progression time were observed without any indication of apoptosis, senescence, or alterations in migration or attachment properties. Combined knockdown of BRM and BRG1 showed additive effects in the reduction of cell proliferation and time required for completion of cell cycle, suggesting that these enzymes promote cell cycle progression through independent mechanisms. Knockout of BRG1 or BRM using CRISPR/Cas9 technology resulted in the loss of viability, consistent with a requirement for both enzymes in triple negative breast cancer cells.</p>
dc.identifier.submissionpathcellbiology_pp/155
dc.contributor.departmentDepartment of Cell and Developmental Biology
dc.source.pages2683-94


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