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Molecular Genetics of the Pi3k-Akt-Mtor Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities Publisher Pubmed



Vahidnezhad H1, 2 ; Youssefian L1, 3 ; Uitto J1
Authors
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Authors Affiliations
  1. 1. Department of Dermatology and Cutaneous Biology, Sidney Kimmel Medical College, Thomas Jefferson University, 233 South 10th Street, Philadelphia, 19107, PA, United States
  2. 2. Biotechnology Research Center, Department of Molecular Medicine, Pasteur Institute of Iran, Tehran, Iran
  3. 3. Department of Medical Genetics, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Investigative Dermatology Published:2016


Abstract

A number of critical signaling pathways are required for homeostatic regulation of cell survival, differentiation, and proliferation during organogenesis. One of them is the PI3K-AKT-mTOR pathway consisting of a cascade of inhibitor/activator molecules. Recently, a number of heritable diseases with skin involvement, manifesting particularly with tissue overgrowth, have been shown to result from mutations in the genes in the PI3K-AKT-mTOR and interacting intracellular pathways. Many of these conditions represent an overlapping spectrum of phenotypic manifestations forming a basis for novel, unifying classifications. Identification of the mutant genes and specific mutations in these patients has implications for diagnostics and genetic counseling and provides a rational basis for the development of novel treatment modalities for this currently intractable group of disorders. © 2015 The Authors. Published by Elsevier.