Literature DB >> 23384020

Pathogenesis-based therapies in ichthyoses.

Joey E Lai-Cheong1, Peter M Elias, Amy S Paller.   

Abstract

During the past 20 years, tremendous progress has been made in our understanding of the molecular basis of many genetic skin conditions. The translation of these laboratory findings into effective therapies for affected individuals has been slow, however, in large part due to the risk of carcinogenesis from random viral genomic integration and the lack of efficacy of topically applied genetic material and most proteins. As intervention at the gene level still appears remote for most genetic disorders, increased knowledge about the cellular and biochemical pathogenesis of disease allows specific targeting of pathways with existing and/or novel drugs and molecules. In contrast to the requirement for personalization of most gene-based approaches, pathogenesis-based therapy is pathway specific, and in theory, it should have broader applicability. In this chapter, we provide an overview of the pathoetiology of the various types of ichthyoses and demonstrate how a pathogenesis-based approach can potentially lead to innovative treatments for these conditions. Notably, this strategy has been successfully validated for the treatment of the rare X-linked dominant condition, CHILD syndrome, in which topical applications of cholesterol and lovastatin together to affected skin resulted in marked improvement of the skin phenotype.
© 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23384020      PMCID: PMC4498576          DOI: 10.1111/j.1529-8019.2012.01528.x

Source DB:  PubMed          Journal:  Dermatol Ther        ISSN: 1396-0296            Impact factor:   2.851


  73 in total

1.  Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay.

Authors:  Miao He; Lisa E Kratz; Joshua J Michel; Abbe N Vallejo; Laura Ferris; Richard I Kelley; Jacqueline J Hoover; Drazen Jukic; K Michael Gibson; Lynne A Wolfe; Dhanya Ramachandran; Michael E Zwick; Jerry Vockley
Journal:  J Clin Invest       Date:  2011-03       Impact factor: 14.808

2.  Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com.

Authors:  J M Derry; E Gormally; G D Means; W Zhao; A Meindl; R I Kelley; Y Boyd; G E Herman
Journal:  Nat Genet       Date:  1999-07       Impact factor: 38.330

3.  Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome.

Authors:  C Lefèvre; F Jobard; F Caux; B Bouadjar; A Karaduman; R Heilig; H Lakhdar; A Wollenberg; J L Verret; J Weissenbach; M Ozgüc; M Lathrop; J F Prud'homme; J Fischer
Journal:  Am J Hum Genet       Date:  2001-10-02       Impact factor: 11.025

4.  Clinical phenotype of desmosterolosis.

Authors:  D R FitzPatrick; J W Keeling; M J Evans; A E Kan; J E Bell; M E Porteous; K Mills; R M Winter; P T Clayton
Journal:  Am J Med Genet       Date:  1998-01-13

Review 5.  Are side-chain oxidized oxysterols regulators also in vivo?

Authors:  Ingemar Björkhem
Journal:  J Lipid Res       Date:  2008-10-23       Impact factor: 5.922

6.  Autosomal recessive congenital ichthyosis.

Authors:  Judith Fischer
Journal:  J Invest Dermatol       Date:  2009-06       Impact factor: 8.551

7.  Effects of dietary cholesterol and simvastatin on cholesterol synthesis in Smith-Lemli-Opitz syndrome.

Authors:  Yen-Ming Chan; Louise S Merkens; William E Connor; Jean-Baptiste Roullet; Jennifer A Penfield; Julia M Jordan; Robert D Steiner; Peter J H Jones
Journal:  Pediatr Res       Date:  2009-06       Impact factor: 3.756

8.  Stratum corneum lipids in disorders of cornification. Steroid sulfatase and cholesterol sulfate in normal desquamation and the pathogenesis of recessive X-linked ichthyosis.

Authors:  P M Elias; M L Williams; M E Maloney; J A Bonifas; B E Brown; S Grayson; E H Epstein
Journal:  J Clin Invest       Date:  1984-10       Impact factor: 14.808

Review 9.  Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism.

Authors:  Peter M Elias; Mary L Williams; Walter M Holleran; Yan J Jiang; Matthias Schmuth
Journal:  J Lipid Res       Date:  2008-02-02       Impact factor: 5.922

10.  Pathogenesis-based therapy reverses cutaneous abnormalities in an inherited disorder of distal cholesterol metabolism.

Authors:  Amy S Paller; Maurice A M van Steensel; Marina Rodriguez-Martín; Jennifer Sorrell; Candrice Heath; Debra Crumrine; Michel van Geel; Antonio Noda Cabrera; Peter M Elias
Journal:  J Invest Dermatol       Date:  2011-07-14       Impact factor: 8.551

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  5 in total

Review 1.  [Syndroms associated with benign skin tumors].

Authors:  George-Sorin Tiplica; Klaus Fritz; Alexandra Irina Butacu; Loredana Ungureanu; Carmen Maria Sălăvăstru
Journal:  Hautarzt       Date:  2022-01-25       Impact factor: 0.751

Review 2.  Treatments for Non-Syndromic Inherited Ichthyosis, Including Emergent Pathogenesis-Related Therapy.

Authors:  Divina Justina Hasbani; Lamiaa Hamie; Edward Eid; Christel Tamer; Ossama Abbas; Mazen Kurban
Journal:  Am J Clin Dermatol       Date:  2022-08-12       Impact factor: 6.233

3.  Targeting epidermal lipids for treatment of Mendelian disorders of cornification.

Authors:  Dimitra Kiritsi; Franziska Schauer; Ute Wölfle; Manthoula Valari; Leena Bruckner-Tuderman; Cristina Has; Rudolf Happle
Journal:  Orphanet J Rare Dis       Date:  2014-03-07       Impact factor: 4.123

Review 4.  Recent advances in understanding ichthyosis pathogenesis.

Authors:  Nareh V Marukian; Keith A Choate
Journal:  F1000Res       Date:  2016-06-24

5.  Validity of First-Time Diagnoses of Inherited Ichthyosis in the Danish National Patient Registry and the Danish Pathology Registry.

Authors:  Mattias Hedegaard Kristensen; Sigrun Alba Johannesdottir Schmidt; Line Kibsgaard; Hanne Hove; Mette Sommerlund; Uffe Koppelhus
Journal:  Clin Epidemiol       Date:  2020-06-19       Impact factor: 4.790

  5 in total

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