Transcriptome-wide Profiling of Cerebral Cavernous Malformations Patients Reveal Important Long noncoding RNA molecular signatures.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
03 12 2019
Historique:
received: 25 09 2019
accepted: 20 11 2019
entrez: 5 12 2019
pubmed: 5 12 2019
medline: 11 11 2020
Statut: epublish

Résumé

Cerebral cavernous malformations (CCMs) are low-flow vascular malformations in the brain associated with recurrent hemorrhage and seizures. The current treatment of CCMs relies solely on surgical intervention. Henceforth, alternative non-invasive therapies are urgently needed to help prevent subsequent hemorrhagic episodes. Long non-coding RNAs (lncRNAs) belong to the class of non-coding RNAs and are known to regulate gene transcription and involved in chromatin remodeling via various mechanism. Despite accumulating evidence demonstrating the role of lncRNAs in cerebrovascular disorders, their identification in CCMs pathology remains unknown. The objective of the current study was to identify lncRNAs associated with CCMs pathogenesis using patient cohorts having 10 CCM patients and 4 controls from brain. Executing next generation sequencing, we performed whole transcriptome sequencing (RNA-seq) analysis and identified 1,967 lncRNAs and 4,928 protein coding genes (PCGs) to be differentially expressed in CCMs patients. Among these, we selected top 6 differentially expressed lncRNAs each having significant correlative expression with more than 100 differentially expressed PCGs. The differential expression status of the top lncRNAs, SMIM25 and LBX2-AS1 in CCMs was further confirmed by qRT-PCR analysis. Additionally, gene set enrichment analysis of correlated PCGs revealed critical pathways related to vascular signaling and important biological processes relevant to CCMs pathophysiology. Here, by transcriptome-wide approach we demonstrate that lncRNAs are prevalent in CCMs disease and are likely to play critical roles in regulating important signaling pathways involved in the disease progression. We believe, that detailed future investigations on this set of identified lncRNAs can provide useful insights into the biology and, ultimately, contribute in preventing this debilitating disease.

Identifiants

pubmed: 31796831
doi: 10.1038/s41598-019-54845-0
pii: 10.1038/s41598-019-54845-0
pmc: PMC6890746
doi:

Substances chimiques

RNA, Long Noncoding 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

18203

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Auteurs

Santhilal Subhash (S)

Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, 40530, Sweden.

Norman Kalmbach (N)

Neopep Pharma GmbH & Co. KG, Feodor Lynen Strasse 31, 30625, Hannover, Germany.

Florian Wegner (F)

Department of Neurology, Hannover Medical School, Hannover, Germany.

Susanne Petri (S)

Department of Neurology, Hannover Medical School, Hannover, Germany.

Torsten Glomb (T)

Research Core Unit Genomics, Hannover Medical School, Hannover, Germany.

Oliver Dittrich-Breiholz (O)

Research Core Unit Genomics, Hannover Medical School, Hannover, Germany.

Caiquan Huang (C)

International Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.

Kiran Kumar Bali (KK)

Department for Experimental Pain Research, Center of Biomedicine and Medical Technology Mannheim (CBTM), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Wolfram S Kunz (WS)

Institute of Experimental Epileptology and Cognition Research and Department of Epileptology, Life and Brain Center, University Hospital Bonn, Sigmund-Freud-Strasse 25, D-53105, Bonn, Germany.

Amir Samii (A)

International Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.

Helmut Bertalanffy (H)

International Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.

Chandrasekhar Kanduri (C)

Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, 40530, Sweden. kanduri.chandrasekhar@gu.se.

Souvik Kar (S)

International Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany. kar@ini-hannover.de.

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