| Literature DB >> 30904097 |
Lauren J McEneaney1, Andrew R Tee2.
Abstract
Tuberous sclerosis complex (TSC) is a rare, autosomal dominant genetic condition caused by a mutation in either the TSC1 or TSC2 gene. Phenotypically, this leads to aberrant cell growth and the formation of benign tumors called hamartomas in multiple organs. Understanding the mechanisms of pathology that are caused through the presence of disease causing mutations is a real hurdle for many rare genetic disorders; a limiting factor that restricts knowledge of the disease and any hope of a future cure. Through the discovery of the TSC1 and TSC2 genes and the signaling pathways responsible for the pathology of TSC, a new drug target called mechanistic target of rapamycin complex 1 (mTORC1) was discovered. Rapamycin, an mTORC1 inhibitor, is now the only pharmacological therapy approved for the treatment of TSC. This chapter summarizes the success story of TSC and explores the future possibilities of finding a cure.Entities:
Keywords: ER stress; Energy homeostasis; Rapamycin; TSC; mTOR; mTORC1
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Year: 2018 PMID: 30904097 DOI: 10.1016/bs.adgen.2018.11.003
Source DB: PubMed Journal: Adv Genet ISSN: 0065-2660 Impact factor: 1.944