Literature DB >> 26547211

Molecular medicine of fragile X syndrome: based on known molecular mechanisms.

Shi-Yu Luo1, Ling-Qian Wu1, Ran-Hui Duan2.   

Abstract

BACKGROUND: Extensive research on fragile X mental retardation gene knockout mice and mutant Drosophila models has largely expanded our knowledge on mechanism-based treatment of fragile X syndrome (FXS). In light of these findings, several clinical trials are now underway for therapeutic translation to humans. DATA SOURCES: Electronic literature searches were conducted using the PubMed database and ClinicalTrials.gov. The search terms included "fragile X syndrome", "FXS and medication", "FXS and therapeutics" and "FXS and treatment". Based on the publications identified in this search, we reviewed the neuroanatomical abnormalities in FXS patients and the potential pathogenic mechanisms to monitor the progress of FXS research, from basic studies to clinical trials.
RESULTS: The pathological mechanisms of FXS were categorized on the basis of neuroanatomy, synaptic structure, synaptic transmission and fragile X mental retardation protein (FMRP) loss of function. The neuroanatomical abnormalities in FXS were described to motivate extensive research into the region-specific pathologies in the brain responsible for FXS behavioural manifestations. Mechanism-directed molecular medicines were classified according to their target pathological mechanisms, and the most recent progress in clinical trials was discussed.
CONCLUSIONS: Current mechanism-based studies and clinical trials have greatly contributed to the development of FXS pharmacological therapeutics. Research examining the extent to which these treatments provided a rescue effect or FMRP compensation for the developmental impairments in FXS patients may help to improve the efficacy of treatments.

Entities:  

Keywords:  clinical trial; fragile X syndrome; mechanism-based; treatment

Mesh:

Year:  2015        PMID: 26547211     DOI: 10.1007/s12519-015-0052-0

Source DB:  PubMed          Journal:  World J Pediatr            Impact factor:   2.764


  89 in total

1.  Medication utilization for targeted symptoms in children and adults with fragile X syndrome: US survey.

Authors:  Donald B Bailey; Melissa Raspa; Ellen Bishop; Murrey Olmsted; Usha G Mallya; Elizabeth Berry-Kravis
Journal:  J Dev Behav Pediatr       Date:  2012-01       Impact factor: 2.225

2.  Open-label riluzole in fragile X syndrome.

Authors:  Craig A Erickson; Ning Weng; Ivan Jeanne Weiler; William T Greenough; Kimberly A Stigler; Logan K Wink; Christopher J McDougle
Journal:  Brain Res       Date:  2010-11-05       Impact factor: 3.252

3.  The fragile X mental retardation protein is associated with ribosomes.

Authors:  E W Khandjian; F Corbin; S Woerly; F Rousseau
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330

4.  Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome.

Authors:  S Eliez; C M Blasey; L S Freund; T Hastie; A L Reiss
Journal:  Brain       Date:  2001-08       Impact factor: 13.501

5.  Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging.

Authors:  Jacob Ellegood; Laura K Pacey; David R Hampson; Jason P Lerch; R Mark Henkelman
Journal:  Neuroimage       Date:  2010-03-19       Impact factor: 6.556

6.  Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine.

Authors:  Roberta Pietrobono; Maria Grazia Pomponi; Elisabetta Tabolacci; Ben Oostra; Pietro Chiurazzi; Giovanni Neri
Journal:  Nucleic Acids Res       Date:  2002-07-15       Impact factor: 16.971

Review 7.  Psychopharmacology in fragile X syndrome--present and future.

Authors:  Elizabeth Berry-Kravis; Kristina Potanos
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2004

8.  Chronic metabotropic glutamate receptor 5 inhibition corrects local alterations of brain activity and improves cognitive performance in fragile X mice.

Authors:  Aubin Michalon; Andreas Bruns; Céline Risterucci; Michael Honer; Theresa M Ballard; Laurence Ozmen; Georg Jaeschke; Joseph G Wettstein; Markus von Kienlin; Basil Künnecke; Lothar Lindemann
Journal:  Biol Psychiatry       Date:  2013-07-30       Impact factor: 13.382

9.  Positive AMPA receptor modulation rapidly stimulates BDNF release and increases dendritic mRNA translation.

Authors:  Hussam Jourdi; Yu-Tien Hsu; Miou Zhou; Qingyu Qin; Xiaoning Bi; Michel Baudry
Journal:  J Neurosci       Date:  2009-07-08       Impact factor: 6.167

10.  Genetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome mice.

Authors:  Aditi Bhattacharya; Hanoch Kaphzan; Amanda C Alvarez-Dieppa; Jaclyn P Murphy; Philippe Pierre; Eric Klann
Journal:  Neuron       Date:  2012-10-17       Impact factor: 17.173

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  3 in total

Review 1.  Multifarious Functions of the Fragile X Mental Retardation Protein.

Authors:  Jenna K Davis; Kendal Broadie
Journal:  Trends Genet       Date:  2017-08-18       Impact factor: 11.639

Review 2.  Reactivation of FMR1 gene expression is a promising strategy for fragile X syndrome therapy.

Authors:  Ekaterina M Shitik; Anastasia A Velmiskina; Alexander A Dolskiy; Dmitry V Yudkin
Journal:  Gene Ther       Date:  2020-03-12       Impact factor: 5.250

3.  Association of fragile X syndrome, Robertsonian translocation (13, 22) and autism in a child.

Authors:  Andreea Liana Rachisan; Alexandru Stefan Niculae; Ioana Tintea; Bianca Pop; Mariela Militaru; Aurel Bizo; Adrian Hrusca
Journal:  Clujul Med       Date:  2017-10-20
  3 in total

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