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Patients typically present with advanced disease, and most patients succumb within a decade of diagnosis. There is a clear and urgent need for novel therapeutic approaches that will affect mantle cell lymphoma through a unique mechanism compared to current therapies. This study examined the use of RNA interference (RNAi) therapy to attack mantle cell lymphoma at the mRNA level, silencing genes associated with cancer cell proliferation. We identified a lipid nanoparticle formulated with the lipidoid 306O<jats:sub>13<\/jats:sub> that delivered siRNA to JeKo\u20101 and MAVER\u20101 mantle cell lymphoma cell lines. Three therapeutic gene targets were examined for their effect on lymphoma growth. These included Cyclin D1, which is a cell cycle regulator, as well as Bcl\u20102 and Mcl\u20101, which prevent apoptosis. Gene knockdown with siRNA doses as low at 10 nM increased lymphoma cell apoptosis without carrier\u2010mediated toxicity. Silencing of Cyclin D1 induced apoptosis despite a twofold \u201ccompensation\u201d upregulation of Cyclin D2. Upon simultaneous silencing of all three genes, nearly 75% of JeKo\u20101 cells were apoptosing 3 days post\u2010transfection. Furthermore, cells proliferated at only 15% of their pretreatment rate. These data suggest that lipid nanoparticles\u2010formulated, multiplexed siRNA \u201ccocktails\u201d may serve as a beneficial addition to the treatment regimens for mantle cell lymphoma and other aggressive cancers.<\/jats:p>","DOI":"10.1002\/btm2.10088","type":"journal-article","created":{"date-parts":[[2018,3,7]],"date-time":"2018-03-07T10:48:02Z","timestamp":1520419682000},"page":"138-147","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":24,"title":["Lipid nanoparticle siRNA cocktails for the treatment of mantle cell lymphoma"],"prefix":"10.1002","volume":"3","author":[{"given":"Christopher M.","family":"Knapp","sequence":"first","affiliation":[{"name":"Dept. of Chemical Engineering"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jia","family":"He","sequence":"additional","affiliation":[{"name":"Dept. of Biomedical Engineering Carnegie Mellon University, 5000 Forbes Ave. Pittsburgh PA 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