The effects of Resveratrol and Rapamycin combination on Lymphangioleiomyomatosis cell signaling and survival

dc.contributor.advisorHolz, Marina K.
dc.contributor.authorWachsstock, Davita
dc.date.accessioned2024-11-05T20:29:32Z
dc.date.available2024-11-05T20:29:32Z
dc.date.issued2013-12-16
dc.descriptionUndergraduate honors thesis / YU only
dc.description.abstractis a disease that primarily affects women, and results in tumorous growths that can metastasize to the lungs and cause respiratory failure. Cells from these tumors are deficient in the tumor suppressor TSC2, and therefore show unique gene expression and signaling patterns. In this study we evaluated the therapeutic benefits of combination therapy of Rapamycin and Resveratrol on LAM cells. Rapamycin, a drug currently used to treat LAM patients, is only partially effective because it induces autophagy, a cell survival mechanism, and may actually prevent LAM cell death. Resveratrol, a naturally occurring polyphenol, when used in combination with rapamycin, can inhibit rapamycin-induced autophagy and decrease survival signaling, allowing LAM cells to die by apoptosis. Based on this research, combination therapy of rapamycin and resveratrol may prove an effective clinical treatment for lymphangioleiomyomatosis patients.
dc.description.sponsorshipFunded in part by the S. Daniel Abraham Honors Program
dc.identifier.citationWachsstock, D. (2013). The effects of Resveratrol and Rapamycin combination on Lymphangioleiomyomatosis cell signaling and survival [Unpublished undergraduate honors thesis, Yeshiva University].
dc.identifier.urihttps://hdl.handle.net/20.500.12202/10730
dc.language.isoen_US
dc.publisherYeshiva University
dc.relation.ispartofseriesS. Daniel Abraham Honors Student Theses; December 2013
dc.subjectLymphangioleiomyomatosis (LAM)
dc.subjecttumor suppressor TSC2
dc.subjectRapamycin
dc.subjectResveratrol
dc.subjectpolyphenol
dc.titleThe effects of Resveratrol and Rapamycin combination on Lymphangioleiomyomatosis cell signaling and survival
dc.typeThesis

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