An update on the epigenetics of psychotic diseases and autism.

Abstract:

:The examination of potential roles of epigenetic alterations in the pathogenesis of psychotic diseases have become an essential alternative in recent years as genetic studies alone are yet to uncover major gene(s) for psychosis. Here, we describe the current state of knowledge from the gene-specific and genome-wide studies of postmortem brain and blood cells indicating that aberrant DNA methylation, histone modifications and dysregulation of micro-RNAs are linked to the pathogenesis of mental diseases. There is also strong evidence supporting that all classes of psychiatric drugs modulate diverse features of the epigenome. While comprehensive environmental and genetic/epigenetic studies are uncovering the origins, and the key genes/pathways affected in psychotic diseases, characterizing the epigenetic effects of psychiatric drugs may help to design novel therapies in psychiatry.

journal_name

Epigenomics

journal_title

Epigenomics

authors

Abdolmaleky HM,Zhou JR,Thiagalingam S

doi

10.2217/epi.14.85

subject

Has Abstract

pub_date

2015-01-01 00:00:00

pages

427-49

issue

3

eissn

1750-1911

issn

1750-192X

journal_volume

7

pub_type

杂志文章,评审
  • Sex-specific histone modifications in mouse fetal and neonatal germ cells.

    abstract:AIMS:Epigenetic signatures of germline cells are dynamically reprogrammed to induce appropriate differentiation, development and sex specification. We investigated sex-specific epigenetic changes in mouse fetal germ cells (FGCs) and neonatal germ cells. MATERIALS & METHODS:Six histone marks in mouse E13.5 FGCs and P1 ...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2018-0193

    authors: Kawabata Y,Kamio A,Jincho Y,Sakashita A,Takashima T,Kobayashi H,Matsui Y,Kono T

    更新日期:2019-04-01 00:00:00

  • Epigenetics and brain evolution.

    abstract::Fundamental aspects of mammalian brain evolution occurred in the context of viviparity and placentation brought about by the epigenetic regulation of imprinted genes. Since the fetal placenta hormonally primes the maternal brain, two genomes in one individual are transgenerationally co-adapted to ensure maternal care ...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi.11.10

    authors: Keverne EB

    更新日期:2011-04-01 00:00:00

  • Interview with Stephen B Baylin.

    abstract::Stephen B Baylin is a codirector of the Cancer Biology Program at The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins and the Virginia and DK Ludwig Professor of Oncology and Medicine. Baylin attended Duke University, where he earned his medical degree and completed his internship and first year residency i...

    journal_title:Epigenomics

    pub_type: 面试

    doi:10.2217/epi.15.61

    authors: Baylin SB

    更新日期:2015-01-01 00:00:00

  • An OMIC biomarker detection algorithm TriVote and its application in methylomic biomarker detection.

    abstract:AIM:Transcriptomic and methylomic patterns represent two major OMIC data sources impacted by both inheritable genetic information and environmental factors, and have been widely used as disease diagnosis and prognosis biomarkers. MATERIALS & METHODS:Modern transcriptomic and methylomic profiling technologies detect th...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2017-0097

    authors: Xu C,Liu J,Yang W,Shu Y,Wei Z,Zheng W,Feng X,Zhou F

    更新日期:2018-04-01 00:00:00

  • Pregnancy-associated changes in cervical noncoding RNA.

    abstract::Aim: To identify pregnancy-associated changes in cervical noncoding RNA (ncRNA), including miRNA and long noncoding RNA (lncRNA), and their potential effects on biologic processes. Materials & methods: We enrolled 21 pregnant women with term deliveries (≥37 weeks' gestation) in a prospective cohort and collected cervi...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2019-0231

    authors: Gerson KD,Haviland MJ,Neo D,Hecht JL,Baccarelli AA,Brennan KJ,Dereix AE,Ralston SJ,Hacker MR,Burris HH

    更新日期:2020-06-01 00:00:00

  • Epigenetic protein complexes: the adequate candidates for the use of a new generation of epidrugs in personalized and precision medicine in cancer.

    abstract::Until recently, drug development in oncology was focused on treating most patients for a specific cancer type without taking in account the heterogeneity between these patients in term of response to treatment. Therefore, this type of broad treatment approach excludes the treatment of patient not responding to disease...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2019-0169

    authors: Cartron PF,Cheray M,Bretaudeau L

    更新日期:2020-01-01 00:00:00

  • Maternal obesity is associated with a sex-specific epigenetic programming in human neonatal monocytes.

    abstract::Aim: To determine changes in global DNA methylation in monocytes from neonates of women with obesity, as markers of an immune programming resulting from maternal obesity. Materials & methods: Cord blood monocytes were obtained from neonates born to women with obesity and normal weight, genome-wide differentially methy...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2020-0098

    authors: Vega-Tapia F,Artigas R,Hernández C,Uauy R,Casanello P,Krause BJ,Castro-Rodriguez JA

    更新日期:2020-11-01 00:00:00

  • Role of histone acetylation in gastric cancer: implications of dietetic compounds and clinical perspectives.

    abstract::Histone modifications regulate the structural status of chromatin and thereby influence the transcriptional status of genes. These processes are controlled by the recruitment of different enzymes to a specific genomic site. Furthermore, obtaining an understanding of these mechanisms could help delineate alternative tr...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi-2018-0081

    authors: Calcagno DQ,Wisnieski F,Mota ERDS,Maia de Sousa SB,Costa da Silva JM,Leal MF,Gigek CO,Santos LC,Rasmussen LT,Assumpção PP,Burbano RR,Smith MA

    更新日期:2019-02-01 00:00:00

  • MiR-377 reverses cancerous phenotypes of pancreatic cells via suppressing DNMT1 and demethylating tumor suppressor genes.

    abstract:AIM:The aim was to investigate the effect of miR-377 on DNMT1 expression and cancer phenotype in pancreatic cancer cells. MATERIALS & METHODS:Real-time PCR, luciferase assay, MTT and Annexin-PI staining were used. RESULTS:Decreased miR-377 and increased DNMT1 (verified as a target for mir-377) levels in pancreatic ca...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2016-0175

    authors: Azizi M,Fard-Esfahani P,Mahmoodzadeh H,Fazeli MS,Azadmanesh K,Zeinali S,Teimoori-Toolabi L

    更新日期:2017-08-01 00:00:00

  • Clinical value and potential mechanisms of LINC00221 in hepatocellular carcinoma based on integrated analysis.

    abstract::This study aimed to unveil the functional roles of LINC00221 in hepatocellular carcinoma (HCC). A discovery cohort and a validation cohort were respectively used to identify and verify the clinical value of LINC00221 in HCC. Bioinformatics analysis was performed to explore its potential mechanisms. LINC00221 was upreg...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2020-0363

    authors: Feng Y,Dramani Maman ST,Zhu X,Liu X,Bongolo CC,Liang C,Tu J

    更新日期:2021-01-07 00:00:00

  • Metabolic-epigenetic crosstalk in macrophage activation.

    abstract::Epigenetic enzymes are emerging as crucial controllers of macrophages, innate immune cells that determine the outcome of many inflammatory diseases. Recent studies demonstrate that the activity of particular chromatin-modifying enzymes is regulated by the availability of specific metabolites like acetyl-coenzyme A, S-...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi.15.71

    authors: Baardman J,Licht I,de Winther MP,Van den Bossche J

    更新日期:2015-10-01 00:00:00

  • miRNAs derived from cancer-associated fibroblasts in colorectal cancer.

    abstract::Currently, the incidence of colorectal cancer (CRC) is increasing across the world. The cancer stroma exerts an impact on the spread, invasion and chemoresistance of CRC. The tumor microenvironment involves a complex interaction between cancer cells and stromal cells, for example, cancer-associated fibroblasts (CAFs)....

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi-2019-0110

    authors: Savardashtaki A,Shabaninejad Z,Movahedpour A,Sahebnasagh R,Mirzaei H,Hamblin MR

    更新日期:2019-11-01 00:00:00

  • Epigenetics of kidney cancer and bladder cancer.

    abstract::This article focuses on the epigenetic alterations of aberrant promoter hypermethylation of genes, and histone modifications or RNA interference in cancer cells. Current knowledge of the hypermethylation of allele(s) in classical tumor suppressor genes in inherited and sporadic cancer, candidate tumor suppressor and o...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi.10.64

    authors: Hoffman AM,Cairns P

    更新日期:2011-02-01 00:00:00

  • Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.

    abstract:AIM:To characterize the genotypic and phenotypic extent of multilocus imprinting disturbances (MLID). MATERIALS & METHODS:We analyzed 37 patients with imprinting disorders (explorative cohort) for DNA methylation changes using the Infinium HumanMethylation450 BeadChip. For validation, three independent cohorts with im...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2016-0007

    authors: Bens S,Kolarova J,Beygo J,Buiting K,Caliebe A,Eggermann T,Gillessen-Kaesbach G,Prawitt D,Thiele-Schmitz S,Begemann M,Enklaar T,Gutwein J,Haake A,Paul U,Richter J,Soellner L,Vater I,Monk D,Horsthemke B,Ammerpohl O,

    更新日期:2016-06-01 00:00:00

  • LncRNA HORAS5 promotes taxane resistance in castration-resistant prostate cancer via a BCL2A1-dependent mechanism.

    abstract::Background: Castration-resistant prostate cancer (CRPC) is an incurable malignancy. Long noncoding RNAs (lncRNAs) play key roles in drug resistance. Materials & methods: LncRNA HORAS5 role in cabazitaxel resistance (i.e., cell-count, IC50 and caspase activity) was studied via lentiviral-mediated overexpression and siR...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2019-0316

    authors: Pucci P,Venalainen E,Alborelli I,Quagliata L,Hawkes C,Mather R,Romero I,Rigas SH,Wang Y,Crea F

    更新日期:2020-07-01 00:00:00

  • Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders.

    abstract::The widely accepted association between aberrant methylation at specific imprinted loci and distinct imprinting disorders has recently been brought into question by the identification of methylation defects at multiple loci (multilocus methylation defect [MLMD]). Strikingly, in different imprinting disorders, the same...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi.11.84

    authors: Eggermann T,Leisten I,Binder G,Begemann M,Spengler S

    更新日期:2011-10-01 00:00:00

  • Combinatorial epigenetic mechanisms and efficacy of early breast cancer inhibition by nutritive botanicals.

    abstract:AIM:Aberrant epigenetic events are important contributors to the pathogenesis of different types of cancers and dietary botanicals with epigenetic properties can influence early cancer development leading to cancer prevention effects. We sought to investigate potential combinatorial effects of bioactive dietary compone...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2016-0024

    authors: Li Y,Buckhaults P,Cui X,Tollefsbol TO

    更新日期:2016-08-01 00:00:00

  • Histone lysine trimethylation or acetylation can be modulated by phytoestrogen, estrogen or anti-HDAC in breast cancer cell lines.

    abstract:AIM:The isoflavones genistein, daidzein and equol (daidzein metabolite) have been reported to interact with epigenetic modifications, specifically hypermethylation of tumor suppressor genes. The objective of this study was to analyze and understand the mechanisms by which phytoestrogens act on chromatin in breast cance...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi.12.74

    authors: Dagdemir A,Durif J,Ngollo M,Bignon YJ,Bernard-Gallon D

    更新日期:2013-02-01 00:00:00

  • DNA methylation at the DMPK gene locus is associated with cognitive functions in myotonic dystrophy type 1.

    abstract::Aim: Myotonic dystrophy type 1 (DM1) is caused by an unstable trinucleotide (CTG) expansion at the DMPK gene locus. Cognitive dysfunctions are often observed in the condition. We investigated the association between DMPK blood DNA methylation (DNAm) and cognitive functions in DM1, considering expansion length and vari...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2020-0328

    authors: Breton É,Légaré C,Overend G,Guay SP,Monckton D,Mathieu J,Gagnon C,Richer L,Gallais B,Bouchard L

    更新日期:2020-12-01 00:00:00

  • DNA methylome analysis of acute lymphoblastic leukemia cells reveals stochastic de novo DNA methylation in CpG islands.

    abstract:AIM:To identify regions of aberrant DNA methylation in acute lymphoblastic leukemia (ALL) cells of different subtypes on a genome-wide scale. MATERIALS & METHODS:Whole-genome bisulfite sequencing (WGBS) was used to determine the DNA methylation levels in cells from four pediatric ALL patients of different subtypes. Th...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2016-0052

    authors: Wahlberg P,Lundmark A,Nordlund J,Busche S,Raine A,Tandre K,Rönnblom L,Sinnett D,Forestier E,Pastinen T,Lönnerholm G,Syvänen AC

    更新日期:2016-10-01 00:00:00

  • Long intergenic noncoding RNA 299 methylation in peripheral blood is a biomarker for triple-negative breast cancer.

    abstract:AIM:To identify DNA methylation biomarkers in peripheral blood samples from triple-negative breast cancer (TNBC) patients. MATERIALS & METHODS:We conducted an epigenome-wide association study (EWAS): the most promising markers were identified in 233 TNBC case-control pairs (discovery set) and subsequently validated in...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2018-0121

    authors: Bermejo JL,Huang G,Manoochehri M,Mesa KG,Schick M,Silos RG,Ko YD,Brüning T,Brauch H,Lo WY,Hoheisel JD,Hamann U

    更新日期:2019-01-01 00:00:00

  • Epigenetics of neuromuscular disorders.

    abstract::Neuromuscular disorders are a heterogeneous group of conditions affecting the neuromuscular system. The aim of this article is to review the major epigenetic findings in motor neuron diseases and major hereditary muscular dystrophies. DNA methylation changes are observed in both hereditary and sporadic forms, and comb...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2020-0282

    authors: Coppedè F

    更新日期:2020-12-01 00:00:00

  • Conference Scene: Epigenetic regulation: from mechanism to intervention.

    abstract::The Medical Research Council Clinical Sciences Centre Symposium on Epigenetic Regulation: From Mechanism to Intervention in London, UK, which was held on 20-22 June 2012, attracted 305 participants from around the globe and included 37 speakers and 85 selected poster presentations. The organizing committee, led by Nia...

    journal_title:Epigenomics

    pub_type: 新闻

    doi:10.2217/epi.12.47

    authors: Chatterjee A

    更新日期:2012-10-01 00:00:00

  • Increased correlation between methylation sites in epigenome-wide replication studies: impact on analysis and results.

    abstract:AIM:To show that an increased correlation between CpGs after selection through an epigenome-wide association studies (EWAS) might translate into biased replication results. METHODS:Pairwise correlation coefficients between CpGs selected in two published EWAS, the top hits replication, Bonferroni p-values, Benjamini-Ho...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2017-0073

    authors: Popovic M,Fasanelli F,Fiano V,Biggeri A,Richiardi L

    更新日期:2017-12-01 00:00:00

  • From Prader-Willi syndrome to psychosis: translating parent-of-origin effects into schizophrenia research.

    abstract::Prader-Willi syndrome (PWS) is a relatively rare disorder that originates from paternally inherited deletions and maternal disomy (mUPD) within the 15q11-q13 region or alterations in the PWS imprinting center. Evidence is accumulating that mUPD underlies high prevalence of psychosis among PWS patients. Several genes i...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi.14.52

    authors: Krefft M,Frydecka D,Adamowski T,Misiak B

    更新日期:2014-01-01 00:00:00

  • 5-hydroxymethylcytosine profiling as an indicator of cellular state.

    abstract::DNA methylation is widely studied in the context of cancer. However, the rediscovery of 5-hydroxymethylation of DNA adds a new layer of complexity to understanding the epigenetic basis of development and disease, including carcinogenesis. There have been significant advances in techniques for the detection of 5-hydrox...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi.13.69

    authors: Laird A,Thomson JP,Harrison DJ,Meehan RR

    更新日期:2013-12-01 00:00:00

  • Conference scene: 2nd cancer epigenetics conference.

    abstract::The GTC Cancer Summit: Novel Approaches to Drug Discovery was divided into two parallel tracks: the 2nd Cancer Epigenetics Conference, and the Protein Kinases and Drug Design Conference. The 2nd Cancer Epigenetics Conference focused on exciting changes in drug discovery that include an unprecedented private and public...

    journal_title:Epigenomics

    pub_type:

    doi:10.2217/epi.13.9

    authors: Smith CL

    更新日期:2013-04-01 00:00:00

  • Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.

    abstract::The E3 ubiquitin ligase UBE3A, also known as E6-AP, has a multitude of ascribed functions and targets relevant to human health and disease. Epigenetic regulation of the UBE3A gene by parentally imprinted noncoding transcription within human chromosome 15q11.2-q13.3 is responsible for the maternal-specific effects of 1...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi.15.70

    authors: LaSalle JM,Reiter LT,Chamberlain SJ

    更新日期:2015-10-01 00:00:00

  • Next-generation sequencing technologies for DNA methylation analyses in cancer genomics.

    abstract::For the first time, the development of next-generation sequencing technologies has brought about tools to investigate epigenetic alterations in an unbiased, yet genome-wide approach. The importance of this innovative technology is undeniable since it has already been established that changes in DNA methylation play an...

    journal_title:Epigenomics

    pub_type: 杂志文章,评审

    doi:10.2217/epi.09.50

    authors: Boerno ST,Grimm C,Lehrach H,Schweiger MR

    更新日期:2010-04-01 00:00:00

  • Identification of antisense lncRNAs targeting GSK3β as a regulator in major depressive disorder.

    abstract::Aim: To identify lncRNAs targeting GSK3β in MDD. Materials & methods: The levels of GSK3β and its three targeting lncRNAs (gsk3β antisense AS1, AS2 and AS3) were detected in 52 patients with major depressive disorder (MDD) before and after 8 weeks of escitalopram treatment. The functional study was evaluated using the...

    journal_title:Epigenomics

    pub_type: 杂志文章

    doi:10.2217/epi-2019-0402

    authors: Liu Z,Li X,Chen C,Sun N,Wang Y,Yang C,Xu Y,Xu Y,Zhang K

    更新日期:2020-10-01 00:00:00