Literature DB >> 27389816

New aspects of myofibrillar myopathies.

Rudolf A Kley1, Montse Olivé, Rolf Schröder.   

Abstract

PURPOSE OF REVIEW: Myofibrillar myopathies (MFMs) are hereditary muscle disorders characterized by distinct histopathological features. This review provides an overview of recent research with respect to new disease genes, clinical phenotypes, insights into pathomechanisms and therapeutic strategies. RECENT
FINDINGS: Beyond the known disease genes DES, FLNC, MYOT, CRYAB, ZASP, BAG3, FHL1 and TTN, mutations in PLEC, ACTA1, HSPB8 and DNAJB6 have also been associated with a MFM phenotype. Proteomic analysis revealed new information about the composition of protein aggregates in myotilinopathy and identified a new diagnostic marker. New animal models mirror central aspects of MFM pathology and novel therapeutic strategies for treatment of MFM were evaluated in cell and animal models.
SUMMARY: MFMs are an expanding and numerically significant group of protein aggregate diseases with marked clinical and genetic heterogeneity. Though no specific therapy is currently available, the generation of patient-mimicking cell and animal models now paves the way for the preclinical evaluation of novel therapeutic strategies.

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Year:  2016        PMID: 27389816     DOI: 10.1097/WCO.0000000000000357

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  20 in total

1.  Widespread remodeling of proteome solubility in response to different protein homeostasis stresses.

Authors:  Xiaojing Sui; Douglas E V Pires; Angelique R Ormsby; Dezerae Cox; Shuai Nie; Giulia Vecchi; Michele Vendruscolo; David B Ascher; Gavin E Reid; Danny M Hatters
Journal:  Proc Natl Acad Sci U S A       Date:  2020-01-21       Impact factor: 11.205

2.  Silencing of the Hsp70-specific nucleotide-exchange factor BAG3 corrects the F508del-CFTR variant by restoring autophagy.

Authors:  Darren M Hutt; Sanjay Kumar Mishra; Daniela Martino Roth; Mads Breum Larsen; Frédéric Angles; Raymond A Frizzell; William E Balch
Journal:  J Biol Chem       Date:  2018-07-09       Impact factor: 5.157

3.  The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy".

Authors:  Julia Schuld; Peter F M van der Ven; Anne Schänzer; Elisabeth Schumann; Diana Zengeler; Lisann Gulatz; Giovanni Maroli; Uwe Ahting; Anke Sprengel; Sabine Gräf; Andreas Hahn; Christian Jux; Till Acker; Dieter O Fürst; Stefan Rupp
Journal:  J Muscle Res Cell Motil       Date:  2021-03-12       Impact factor: 2.698

4.  A Window Into the Myofibrillar Myopathy Proteome.

Authors:  Teerin Liewluck
Journal:  Neurol Genet       Date:  2021-05-18

5.  Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy.

Authors:  Rocio Bengoechea; Andrew R Findlay; Ankan K Bhadra; Hao Shao; Kevin C Stein; Sara K Pittman; Jil Aw Daw; Jason E Gestwicki; Heather L True; Conrad C Weihl
Journal:  J Clin Invest       Date:  2020-08-03       Impact factor: 19.456

6.  A novel dominant D109A CRYAB mutation in a family with myofibrillar myopathy affects αB-crystallin structure.

Authors:  Jakub P Fichna; Anna Potulska-Chromik; Przemysław Miszta; Maria Jolanta Redowicz; Anna M Kaminska; Cezary Zekanowski; Sławomir Filipek
Journal:  BBA Clin       Date:  2016-11-11

7.  Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function.

Authors:  Andreas Unger; Lisa Beckendorf; Pierre Böhme; Rudolf Kley; Marion von Frieling-Salewsky; Hanns Lochmüller; Rolf Schröder; Dieter O Fürst; Matthias Vorgerd; Wolfgang A Linke
Journal:  Acta Neuropathol Commun       Date:  2017-09-15       Impact factor: 7.801

8.  A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8.

Authors:  Delphine Bouhy; Manisha Juneja; Istvan Katona; Anne Holmgren; Bob Asselbergh; Vicky De Winter; Tino Hochepied; Steven Goossens; Jody J Haigh; Claude Libert; Chantal Ceuterick-de Groote; Joy Irobi; Joachim Weis; Vincent Timmerman
Journal:  Acta Neuropathol       Date:  2017-08-05       Impact factor: 17.088

9.  The Drosophila CG1674 gene encodes a synaptopodin 2-like related protein that localizes to the Z-disc and is required for normal flight muscle development and function.

Authors:  Emily R Czajkowski; Marilyn Cisneros; Bianca S Garcia; Jim Shen; Richard M Cripps
Journal:  Dev Dyn       Date:  2020-09-17       Impact factor: 3.780

10.  FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data.

Authors:  Rudolf Andre Kley; Yvonne Leber; Bertold Schrank; Heidi Zhuge; Zacharias Orfanos; Julius Kostan; Adekunle Onipe; Dominik Sellung; Anne Katrin Güttsches; Britta Eggers; Frank Jacobsen; Wolfram Kress; Katrin Marcus; Kristina Djinovic-Carugo; Peter F M van der Ven; Dieter O Fürst; Matthias Vorgerd
Journal:  Neurol Genet       Date:  2021-05-18
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