Literature DB >> 29286471

In Vitro Enzyme Measurement to Test Pharmacological Chaperone Responsiveness in Fabry and Pompe Disease.

Jan Lukas1, Anne-Marie Knospe2, Susanne Seemann2, Valentina Citro3, Maria V Cubellis3, Arndt Rolfs4.   

Abstract

The use of personalized medicine to treat rare monogenic diseases like lysosomal storage disorders (LSDs) is challenged by complex clinical trial designs, high costs, and low patient numbers. Hundreds of mutant alleles are implicated in most of the LSDs. The diseases are typically classified into 2 to 3 different clinical types according to severity. Moreover, molecular characterization of the genotype can help predict clinical outcomes and inform patient care. Therefore, we developed a simple cell culture assay based on HEK293H cells heterologously over-expressing the mutations identified in Fabry and Pompe disease. A similar assay has recently been introduced as a preclinical test to identify amenable mutations for Pharmacological Chaperone Therapy (PCT) in Fabry disease. This manuscript describes an amended cell culture assay which enables rapid phenotypic assessment of allelic variants in Fabry and Pompe disease to identify eligible patients for PCT and may aid in the development of novel pharmacochaperones.

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Year:  2017        PMID: 29286471      PMCID: PMC5755676          DOI: 10.3791/56550

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  25 in total

1.  Quantitative correlation between the residual activity of beta-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease.

Authors:  P Leinekugel; S Michel; E Conzelmann; K Sandhoff
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

2.  α-Galactosidase aggregation is a determinant of pharmacological chaperone efficacy on Fabry disease mutants.

Authors:  Aleksandra Siekierska; Greet De Baets; Joke Reumers; Rodrigo Gallardo; Stanislav Rudyak; Kerensa Broersen; Jose Couceiro; Joost Van Durme; Joost Schymkowitz; Frederic Rousseau
Journal:  J Biol Chem       Date:  2012-07-06       Impact factor: 5.157

3.  Structural and biochemical studies on Pompe disease and a "pseudodeficiency of acid alpha-glucosidase".

Authors:  Youichi Tajima; Fumiko Matsuzawa; Sei-Ichi Aikawa; Toshika Okumiya; Michiru Yoshimizu; Takahiro Tsukimura; Masahiko Ikekita; Seiichi Tsujino; Akihiko Tsuji; Tim Edmunds; Hitoshi Sakuraba
Journal:  J Hum Genet       Date:  2007-09-06       Impact factor: 3.172

4.  Screening for pharmacological chaperones in Fabry disease.

Authors:  Sang-Hoon Shin; Gary J Murray; Stefanie Kluepfel-Stahl; Adele M Cooney; Jane M Quirk; Raphael Schiffmann; Roscoe O Brady; Christine R Kaneski
Journal:  Biochem Biophys Res Commun       Date:  2007-05-22       Impact factor: 3.575

Review 5.  Pharmacological Chaperone Therapy: Preclinical Development, Clinical Translation, and Prospects for the Treatment of Lysosomal Storage Disorders.

Authors:  Giancarlo Parenti; Generoso Andria; Kenneth J Valenzano
Journal:  Mol Ther       Date:  2015-04-16       Impact factor: 11.454

6.  Fabry_CEP: a tool to identify Fabry mutations responsive to pharmacological chaperones.

Authors:  Marco Cammisa; Antonella Correra; Giuseppina Andreotti; Maria Vittoria Cubellis
Journal:  Orphanet J Rare Dis       Date:  2013-07-24       Impact factor: 4.123

Review 7.  The Large Phenotypic Spectrum of Fabry Disease Requires Graduated Diagnosis and Personalized Therapy: A Meta-Analysis Can Help to Differentiate Missense Mutations.

Authors:  Valentina Citro; Marco Cammisa; Ludovica Liguori; Chiara Cimmaruta; Jan Lukas; Maria Vittoria Cubellis; Giuseppina Andreotti
Journal:  Int J Mol Sci       Date:  2016-12-01       Impact factor: 5.923

8.  Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study.

Authors:  Derralynn A Hughes; Kathleen Nicholls; Suma P Shankar; Gere Sunder-Plassmann; David Koeller; Khan Nedd; Gerard Vockley; Takashi Hamazaki; Robin Lachmann; Toya Ohashi; Iacopo Olivotto; Norio Sakai; Patrick Deegan; David Dimmock; François Eyskens; Dominique P Germain; Ozlem Goker-Alpan; Eric Hachulla; Ana Jovanovic; Charles M Lourenco; Ichiei Narita; Mark Thomas; William R Wilcox; Daniel G Bichet; Raphael Schiffmann; Elizabeth Ludington; Christopher Viereck; John Kirk; Julie Yu; Franklin Johnson; Pol Boudes; Elfrida R Benjamin; David J Lockhart; Carrolee Barlow; Nina Skuban; Jeffrey P Castelli; Jay Barth; Ulla Feldt-Rasmussen
Journal:  J Med Genet       Date:  2016-11-10       Impact factor: 6.318

9.  A chaperone enhances blood α-glucosidase activity in Pompe disease patients treated with enzyme replacement therapy.

Authors:  Giancarlo Parenti; Simona Fecarotta; Giancarlo la Marca; Barbara Rossi; Serena Ascione; Maria Alice Donati; Lucia Ovidia Morandi; Sabrina Ravaglia; Anna Pichiecchio; Daniela Ombrone; Michele Sacchini; Maria Barbara Pasanisi; Paola De Filippi; Cesare Danesino; Roberto Della Casa; Alfonso Romano; Carmine Mollica; Margherita Rosa; Teresa Agovino; Edoardo Nusco; Caterina Porto; Generoso Andria
Journal:  Mol Ther       Date:  2014-07-23       Impact factor: 11.454

10.  The pharmacological chaperone AT2220 increases the specific activity and lysosomal delivery of mutant acid alpha-glucosidase, and promotes glycogen reduction in a transgenic mouse model of Pompe disease.

Authors:  Richie Khanna; Allan C Powe; Yi Lun; Rebecca Soska; Jessie Feng; Rohini Dhulipala; Michelle Frascella; Anadina Garcia; Lee J Pellegrino; Su Xu; Nastry Brignol; Matthew J Toth; Hung V Do; David J Lockhart; Brandon A Wustman; Kenneth J Valenzano
Journal:  PLoS One       Date:  2014-07-18       Impact factor: 3.240

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  3 in total

1.  Challenging popular tools for the annotation of genetic variations with a real case, pathogenic mutations of lysosomal alpha-galactosidase.

Authors:  Chiara Cimmaruta; Valentina Citro; Giuseppina Andreotti; Ludovica Liguori; Maria Vittoria Cubellis; Bruno Hay Mele
Journal:  BMC Bioinformatics       Date:  2018-11-30       Impact factor: 3.169

2.  Assessment of Gene Variant Amenability for Pharmacological Chaperone Therapy with 1-Deoxygalactonojirimycin in Fabry Disease.

Authors:  Jan Lukas; Chiara Cimmaruta; Ludovica Liguori; Supansa Pantoom; Katharina Iwanov; Janine Petters; Christina Hund; Maik Bunschkowski; Andreas Hermann; Maria Vittoria Cubellis; Arndt Rolfs
Journal:  Int J Mol Sci       Date:  2020-01-31       Impact factor: 5.923

Review 3.  Pharmacological Chaperones: A Therapeutic Approach for Diseases Caused by Destabilizing Missense Mutations.

Authors:  Ludovica Liguori; Maria Monticelli; Mariateresa Allocca; Bruno Hay Mele; Jan Lukas; Maria Vittoria Cubellis; Giuseppina Andreotti
Journal:  Int J Mol Sci       Date:  2020-01-13       Impact factor: 5.923

  3 in total

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