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dc.contributor.authorHosios, Aaron M
dc.contributor.authorVander Heiden, Matthew G
dc.date.accessioned2021-10-27T19:57:35Z
dc.date.available2021-10-27T19:57:35Z
dc.date.issued2018
dc.identifier.urihttps://hdl.handle.net/1721.1/134001
dc.description.abstractCell growth and division require nutrients, and proliferating cells use a variety of sources to acquire the amino acids, lipids, and nucleotides that support macromolecule synthesis. Lipids are more reduced than other nutrients, whereas nucleotides and amino acids are typically more oxidized. Cells must therefore generate reducing and oxidizing (redox) equivalents to convert consumed nutrients into biosynthetic precursors. To that end, redox cofactor metabolism plays a central role in meeting cellular redox requirements. In this Minireview, we highlight the biosynthetic pathways that involve redox reactions and discuss their integration with metabolism in proliferating mammalian cells.
dc.language.isoen
dc.publisherElsevier BV
dc.relation.isversionof10.1074/JBC.TM117.000239
dc.rightsCreative Commons Attribution 4.0 International license
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceAmerican Society for Biochemistry & Molecular Biology (ASBMB)
dc.titleThe redox requirements of proliferating mammalian cells
dc.typeArticle
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.relation.journalJournal of Biological Chemistry
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-08-03T15:52:59Z
dspace.orderedauthorsHosios, AM; Vander Heiden, MG
dspace.date.submission2021-08-03T15:53:00Z
mit.journal.volume293
mit.journal.issue20
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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