Literature DB >> 28616776

Evidence towards RNA Binding Motif (RNP1, RRM) Protein 3 (RBM3) as a Potential Biomarker of Lithium Response in Bipolar Disorder Patients.

Eleni Merkouri Papadima1, Paola Niola1, Carla Melis1, Claudia Pisanu1, Donatella Congiu1, Cristiana Cruceanu2, Juan Pablo Lopez2, Gustavo Turecki2, Raffaella Ardau3, Giovanni Severino1, Caterina Chillotti3, Maria Del Zompo1,3, Alessio Squassina4.   

Abstract

Lithium has been used for more than six decades for the management of bipolar disorder (BD). In a previous transcriptomic study, we showed that patients affected by either BD or cluster headache, both disorders characterized by circadian disturbances and response to lithium in a subgroup of patients, have higher expression of the RNA binding motif (RNP1, RRM) protein 3 (RBM3) gene compared to controls. To investigate whether RBM3 could represent a biomarker of lithium response, we screened raw microarray expression data from lymphoblastoid cell lines (LCLs) derived from 20 BD patients, responders or non-responders to lithium. RBM3 was the most significantly differentially expressed gene in the list, being overexpressed in responders compared to non-responders (fold change = 2.0; p = 1.5 × 10-16). We therefore sought to validate the microarray finding by quantitative reverse transcription polymerase chain reaction (RT-qPCR) and explore whether RBM3 expression was modulated by lithium treatment in vitro in LCLs as well as in human-derived neural progenitor cells (NPCs). Our findings confirmed the higher expression of RBM3 in responders compared to non-responders (fold change = 3.78; p = 0.0002). Lithium did not change RBM3 expression in LCLs in any of the groups, but it increased its expression in NPCs. While preliminary, our data suggest that higher levels of RBM3 might be required for better lithium response and that the expression of this gene could be modulated by lithium in a tissue-specific manner.

Entities:  

Keywords:  Bipolar disorder; Circadian rhythm; Gene expression; Lithium response; Mood stabilizers; Neuroprotection

Mesh:

Substances:

Year:  2017        PMID: 28616776     DOI: 10.1007/s12031-017-0938-5

Source DB:  PubMed          Journal:  J Mol Neurosci        ISSN: 0895-8696            Impact factor:   3.444


  32 in total

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6.  Preliminary Transcriptome Analysis in Lymphoblasts from Cluster Headache and Bipolar Disorder Patients Implicates Dysregulation of Circadian and Serotonergic Genes.

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Journal:  J Mol Neurosci       Date:  2015-04-28       Impact factor: 3.444

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Authors:  Alessio Squassina; Marta Costa; Donatella Congiu; Mirko Manchia; Andrea Angius; Valeria Deiana; Raffaella Ardau; Caterina Chillotti; Giovanni Severino; Stefano Calza; Maria Del Zompo
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Review 4.  Protein Translation and Psychiatric Disorders.

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6.  Whole Genome Expression Analyses of miRNAs and mRNAs Suggest the Involvement of miR-320a and miR-155-3p and their Targeted Genes in Lithium Response in Bipolar Disorder.

Authors:  Claudia Pisanu; Eleni Merkouri Papadima; Carla Melis; Donatella Congiu; Annalisa Loizedda; Nicola Orrù; Stefano Calza; Sandro Orrù; Carlo Carcassi; Giovanni Severino; Raffaella Ardau; Caterina Chillotti; Maria Del Zompo; Alessio Squassina
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7.  Evidence that genes involved in hedgehog signaling are associated with both bipolar disorder and high BMI.

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  7 in total

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