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      Advances in the therapeutic use of mammalian target of rapamycin (mTOR) inhibitors in dermatology.

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          Abstract

          Significant developments in the use of mammalian target of rapamycin (mTOR) inhibitors (mTORIs) as immunosuppressant and antiproliferative agents have been made. Recent advances in the understanding of the mTOR signaling pathway and its downstream effects on tumorigenesis and vascular proliferation have broadened the clinical applications of mTORIs in many challenging disorders such as tuberous sclerosis complex, pachyonychia congenita, complex vascular anomalies, and inflammatory dermatoses. Systemic mTORI therapy has shown benefits in these areas, but is associated with significant side effects that sometimes necessitate drug holidays. To mitigate the side effects of systemic mTORIs for dermatologic applications, preliminary work to assess the potential of percutaneous therapy has been performed, and the evidence suggests that percutaneous delivery of mTORIs may allow for effective long-term therapy while avoiding systemic toxicities. Additional large placebo-controlled, double-blinded, randomized studies are needed to assess the efficacy, safety, duration, and tolerability of topical treatments. The objective of this review is to provide updated information on the novel use of mTORIs in the management of many cutaneous disorders.

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          Author and article information

          Journal
          J Am Acad Dermatol
          Journal of the American Academy of Dermatology
          Elsevier BV
          1097-6787
          0190-9622
          May 2015
          : 72
          : 5
          Affiliations
          [1 ] Stanford University School of Medicine, Palo Alto, California.
          [2 ] Cambridge Mansions, London, United Kingdom.
          [3 ] Dermatology, Stanford University School of Medicine, Palo Alto, California; Pediatrics, Stanford University School of Medicine, Palo Alto, California; Pediatric Dermatology, Stanford University School of Medicine, Palo Alto, California; Stanford University School of Medicine, Palo Alto, California. Electronic address: jteng3@stanford.edu.
          Article
          S0190-9622(15)00054-7
          10.1016/j.jaad.2015.01.014
          25769191
          535092ce-5068-4e3c-b264-859466538a43
          Copyright © 2015 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.
          History

          antiproliferative,autoimmune,drug repurposing,genodermatosis,immunosuppression,inflammatory,mammalian target of rapamycin,neoplasia,percutaneous therapy,rapamycin,sirolimus,vascular anomalies

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