[an error occurred while processing this directive] ����Ƥ���Բ�ѧ��־ 2006, 32(6) 377-379 DOI:     ISSN: 2096-5540 CN: 32-1880/R

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PubMed
Article by HE Yu-qing
Article by ZHANG Xi-bao
Article by ZENG Kang

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Advances on Epidermolytic Hyperkeratosis and Therapeutic Mechanism with Retinoids

Department of Dermatology, Guangzhou Institute of Dermatology, Guangzhou 510095, China

Department of Dermatology, Guangzhou Institute of Dermatology, Guangzhou 510095, China

Abstract:

Epidermolytic hyperkeratosis is a rare autosome dominantly inherited skin disorder with the presentations of erythroderma and hyperkeratosis. Mutations have been found in the genes of keratin 1 (K1), K10 or K2e. The clinical studies confirm that the skin lesions obviously improve with systemic or topical retinoids. The etiology, pathogenesis, and therapeutic mechanism of retiniods in epidermolytic hyperkeratosis are reviewed.

Keywords: Hyperkeratosis epidermolytic   Retinoids   Keratin  
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[1] Lacz NL,Schwartz RA,Kihiczak G.Epidermolytic hyperkeratosis:a keratin 1 or 10 mutational event.Int J Dermatol,2005,44:1-6.
[2] Uezato H,Yamamoto Y,Kuwae C,et al.A case of bullous congenital ichthyosiform erythroderma (BCIE) caused by a mutation in the lA helix initiation motif of keratin 1.J Dermatol,2005,32:801-808.
[3] Arin MJ,Longley MA,Epstein EH Jr,et al.Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis.Exp Dermatol,2000,9:16-19.
[4] Tal O,Bergman R,Alcalay J,et al.Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1.Clin Exp Dermatol,2005,30:64-67.
[5] Akiyama M,Tsuji-Abe Y,Yanagihara M,et al.Ichthyosis bullosa of Siemens:its correct diagnosis facilitated by molecular genetic testing.Br J Dermatol,2005,152:1353-1356.
[6] Moss C.Cytogenetic and molecular evidence for cutaneous mosaicism:the ectodermal origin of Blaschko lines.Am J Med Genet,1999,85:330-333.
[7] Sun XK,Ma LL,Xie YQ,et al.Keratin 1 and keratin 10 mutations causing epidermolytic hyperkeratosis in Chinese patients.J Dermatol Sci,2002,29:195-200.
[8] Arin MJ,Roop DR.Inducible mouse models for inherited skin diseases:implications for skin gene therapy.Cells Tissues Organs,2004,177:160-168.
[9] Porter RM,Reichelt J,Lunny DP,et al.The relationship between hyperproliferation and epidermal thickening in a mouse model for BCIE.J Invest Dermatol,1998,110:951-957.
[10] Leigh IM,Navsaria H,Purkis PE,et al.Keratins (K16 and K17) as markers of keratinocyte hyperproliferation in psoriasis in vivo and in vitro.Br J Dermatol,1995,133:501-511.
[11] Ekanayake-Mudiyanselage S,Aschauer H,Schmook FP,et al.Expression of epidermal keratins and the comified envelope protein involucrin is influenced by permeability barrier disruption.J Invest Dermatol,1998,111:517-523.
[12] Egberts F,Heinrich M,Jensen JM,et al.Cathepsin D is involved in the regulation oftransglutaminase 1 and epidermal differentiation.J Cell Sci,2004,117(Pt 11):2295-2307.
[13] Virtanen M,Gedde-Dahl T Jr,Mork NJ,et al.Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression.Acta Derm Venereol,2001,81:163-170.
[14] Katugampola RP,Finlay AY.Oral retinoid therapy for disorders of keratinization:single-centre retrospective 25 years' experience on 23patients.Br J Dermatol,2006,154:267-276.
[15] Tomic-Canic M,Freedberg IM,Blumenberg M.Codominant regulation of keratin gene expression by cell surface receptors and nuclear receptors.Exp Cell Res,1996,224:96-102.
[16] Sinha S,Degenstein L,Copenhaver C,et al.Defining the regulatory factors required for epidermal gene expression.Mol Cell Biol,2000,20:2543-2555.
[17] Eckert RL,Crish JF,Robinson NA.The epidermal keratinocyte as a model for the study of gene regulation and cell differentiation.Physiol Rev,1997,77:397-424.
[18] Chakravarti N,E1-Naggar AK,Lotan R,et al.Expression ofretinoid receptors in sebaceous cell carcinoma.J Cutan Pathol,2006,33:10-17.
[19] Chen JY,Penco S,Ostrowski J,et al.RAR-specific agonist/antagonists which dissociate transactivation and AP1 transrepression inhibit anchorage-independent cell proliferation.EMBO J,1995,14:1187-1197.
[20] Crowe DL.Retinoic acid mediates post-transcriptional regulation of keratin 19 mRNA levels.J Cell Sci,1993,106 (Pt 1):183-188.
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