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dc.contributor.authorNickerson, Jeffrey A.
dc.contributor.authorWu, Qiong
dc.contributor.authorImbalzano, Anthony N.
dc.date2022-08-11T08:09:20.000
dc.date.accessioned2022-08-23T16:27:06Z
dc.date.available2022-08-23T16:27:06Z
dc.date.issued2017-04-04
dc.date.submitted2017-05-25
dc.identifier.citationFront Oncol. 2017 Apr 4;7:49. doi: 10.3389/fonc.2017.00049. eCollection 2017. <a href="https://doi.org/10.3389/fonc.2017.00049">Link to article on publisher's site</a>
dc.identifier.issn2234-943X (Linking)
dc.identifier.doi10.3389/fonc.2017.00049
dc.identifier.pmid28421159
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36706
dc.description.abstractTumor cells reprogram their metabolism to survive and grow in a challenging microenvironment. Some of this reprogramming is performed by epigenetic mechanisms. Epigenetics is in turn affected by metabolism; chromatin modifying enzymes are dependent on substrates that are also key metabolic intermediates. We have shown that the chromatin remodeling enzyme Brahma-related gene 1 (BRG1), an epigenetic regulator, is necessary for rapid breast cancer cell proliferation. The mechanism for this requirement is the BRG1-dependent transcription of key lipogenic enzymes and regulators. Reduction in lipid synthesis lowers proliferation rates, which can be restored by palmitate supplementation. This work has established BRG1 as an attractive target for breast cancer therapy. Unlike genetic alterations, epigenetic mechanisms are reversible, promising gentler therapies without permanent off-target effects at distant sites.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28421159&dopt=Abstract">Link to Article in PubMed</a>
dc.rightsCopyright: © 2017 Nickerson, Wu and Imbalzano.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectSMARCA4
dc.subjectSWI/SNF
dc.subjectbreast cancer
dc.subjectcancer metabolism
dc.subjectchromatin remodeling
dc.subjectepigenetic regulation
dc.subjectfatty acid synthesis pathway
dc.subjectBiochemistry
dc.subjectCancer Biology
dc.subjectCell Biology
dc.subjectCellular and Molecular Physiology
dc.subjectMolecular Biology
dc.subjectOncology
dc.titleMammalian SWI/SNF Enzymes and the Epigenetics of Tumor Cell Metabolic Reprogramming
dc.typeJournal Article
dc.source.journaltitleFrontiers in oncology
dc.source.volume7
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1073&amp;context=metnet_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/metnet_pubs/74
dc.identifier.contextkey10212135
refterms.dateFOA2022-08-23T16:27:06Z
html.description.abstract<p>Tumor cells reprogram their metabolism to survive and grow in a challenging microenvironment. Some of this reprogramming is performed by epigenetic mechanisms. Epigenetics is in turn affected by metabolism; chromatin modifying enzymes are dependent on substrates that are also key metabolic intermediates. We have shown that the chromatin remodeling enzyme Brahma-related gene 1 (BRG1), an epigenetic regulator, is necessary for rapid breast cancer cell proliferation. The mechanism for this requirement is the BRG1-dependent transcription of key lipogenic enzymes and regulators. Reduction in lipid synthesis lowers proliferation rates, which can be restored by palmitate supplementation. This work has established BRG1 as an attractive target for breast cancer therapy. Unlike genetic alterations, epigenetic mechanisms are reversible, promising gentler therapies without permanent off-target effects at distant sites.</p>
dc.identifier.submissionpathmetnet_pubs/74
dc.contributor.departmentImbalzano Lab
dc.contributor.departmentNickerson Lab
dc.contributor.departmentDepartment of Radiology
dc.contributor.departmentUMass Metabolic Network
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentDepartment of Pediatrics
dc.contributor.departmentDepartment of Cell and Developmental Biology
dc.source.pages49


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Copyright: © 2017 Nickerson, Wu and Imbalzano.
Except where otherwise noted, this item's license is described as Copyright: © 2017 Nickerson, Wu and Imbalzano.