Literature DB >> 14974080

The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis.

Chelsee Hewitt1, Derek McCormick, Gerry Linden, Dusan Turk, Igor Stern, Ian Wallace, Louise Southern, Liqun Zhang, Rebecca Howard, Pedro Bullon, Melanie Wong, Richard Widmer, Khaled Abdul Gaffar, Lama Awawdeh, Jim Briggs, Reza Yaghmai, Ethlin W Jabs, Peter Hoeger, Oliver Bleck, Stefan G Rüdiger, Gregor Petersilka, Maurizio Battino, Peter Brett, Faiez Hattab, Mohamed Al-Hamed, Philip Sloan, Carmel Toomes, Mike Dixon, Jacqueline James, Andrew P Read, Nalin Thakker.   

Abstract

We have previously reported that loss-of-function mutations in the cathepsin C gene (CTSC) result in Papillon-Lefèvre syndrome, an autosomal recessive condition characterized by palmoplantar keratosis and early-onset, severe periodontitis. Others have also reported CTSC mutations in patients with severe prepubertal periodontitis, but without any skin manifestations. The possible role of CTSC variants in more common types of non-mendelian, early-onset, severe periodontitis ("aggressive periodontitis") has not been investigated. In this study, we have investigated the role of CTSC in all three conditions. We demonstrate that PLS is genetically homogeneous and the mutation spectrum that includes three novel mutations (c.386T>A/p.V129E, c.935A>G/p.Q312R, and c.1235A>G/p.Y412C) in 21 PLS families (including eight from our previous study) provides an insight into structure-function relationships of CTSC. Our data also suggest that a complete loss-of-function appears to be necessary for the manifestation of the phenotype, making it unlikely that weak CTSC mutations are a cause of aggressive periodontitis. This was confirmed by analyses of the CTSC activity in 30 subjects with aggressive periodontitis and age-sex matched controls, which demonstrated that there was no significant difference between these two groups (1,728.7 +/- SD 576.8 micro moles/mg/min vs. 1,678.7 +/- SD 527.2 micro moles/mg/min, respectively, p = 0.73). CTSC mutations were detected in only one of two families with prepubertal periodontitis; these did not form a separate functional class with respect to those observed in classical PLS. The affected individuals in the other prepubertal periodontitis family not only lacked CTSC mutations, but in addition did not share the haplotypes at the CTSC locus. These data suggest that prepubertal periodontitis is a genetically heterogeneous disease that, in some families, just represents a partially penetrant PLS. Copyright 2004 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14974080     DOI: 10.1002/humu.10314

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  18 in total

1.  Novel cathepsin C mutation in a Brazilian family with Papillon-Lefèvre syndrome: case report and mutation update.

Authors:  Debora Pallos; Ana Carolina Acevedo; Heliana Dantas Mestrinho; Ilia Cordeiro; Thomas C Hart
Journal:  J Dent Child (Chic)       Date:  2010 Jan-Apr

2.  Epithelial desquamation observed in a phase I study of an oral cathepsin C inhibitor (GSK2793660).

Authors:  Bruce E Miller; Ruth J Mayer; Navin Goyal; Joanne Bal; Nigel Dallow; Malcolm Boyce; Donald Carpenter; Alison Churchill; Teresa Heslop; Aili L Lazaar
Journal:  Br J Clin Pharmacol       Date:  2017-09-20       Impact factor: 4.335

3.  Cytokine production by leukocytes of Papillon-Lefèvre syndrome patients in whole blood cultures.

Authors:  Christian D Sadik; Barbara Noack; Beate Schacher; Josef Pfeilschifter; Heiko Mühl; Peter Eickholz
Journal:  Clin Oral Investig       Date:  2011-03-05       Impact factor: 3.573

4.  Complementary Experimental Methods in Genetics Open Up New Avenues of Research to Elucidate the Pathogenesis of Periodontitis.

Authors:  Arne S Schaefer
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 2.622

5.  Papillon-Lefèvre syndrome patient reveals species-dependent requirements for neutrophil defenses.

Authors:  Ole E Sørensen; Stine N Clemmensen; Sara L Dahl; Ole Østergaard; Niels H Heegaard; Andreas Glenthøj; Finn Cilius Nielsen; Niels Borregaard
Journal:  J Clin Invest       Date:  2014-09-17       Impact factor: 14.808

6.  Roles of the host oxidative immune response and bacterial antioxidant rubrerythrin during Porphyromonas gingivalis infection.

Authors:  Piotr Mydel; Yusuke Takahashi; Hiromichi Yumoto; Maryta Sztukowska; Malgorzata Kubica; Frank C Gibson; Donald M Kurtz; Jim Travis; L Vincent Collins; Ky-Anh Nguyen; Caroline Attardo Genco; Jan Potempa
Journal:  PLoS Pathog       Date:  2006-07       Impact factor: 6.823

7.  GeneFriends: an online co-expression analysis tool to identify novel gene targets for aging and complex diseases.

Authors:  Sipko van Dam; Rui Cordeiro; Thomas Craig; Jesse van Dam; Shona H Wood; João Pedro de Magalhães
Journal:  BMC Genomics       Date:  2012-10-06       Impact factor: 3.969

Review 8.  Human immunodeficiency syndromes affecting human natural killer cell cytolytic activity.

Authors:  Hyoungjun Ham; Daniel D Billadeau
Journal:  Front Immunol       Date:  2014-01-21       Impact factor: 7.561

9.  Are proteinase 3 and cathepsin C enzymes related to pathogenesis of periodontitis?

Authors:  Oya Türkoğlu; Elif Azarsız; Gülnur Emingil; Necil Kütükçüler; Gül Atilla
Journal:  Biomed Res Int       Date:  2014-05-19       Impact factor: 3.411

Review 10.  CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update.

Authors:  Nikoletta Nagy; Péter Vályi; Zsanett Csoma; Adrienn Sulák; Kornélia Tripolszki; Katalin Farkas; Ekaterine Paschali; Ferenc Papp; Lola Tóth; Beáta Fábos; Lajos Kemény; Katalin Nagy; Márta Széll
Journal:  Mol Genet Genomic Med       Date:  2014-02-11       Impact factor: 2.183

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.