Literature DB >> 35668131

Deep sequencing unveils altered cardiac miRNome in congenital heart disease.

Vinu Ramachandran1, Sambhavi Bhagavatheeswaran1, Sambantham Shanmugam1,2, Madavan Vasudevan3, Malathi Ragunathan1, Kotturathu Mammen Cherian4, Arasambattu Kannan Munirajan1, Sudesh Ravi1, Anandan Balakrishnan5.   

Abstract

Congenital heart disease (CHD) surges from fetal cardiac dysmorphogenesis and chiefly contributes to perinatal morbidity and cardiovascular disease mortality. A continual rise in prevalence and prerequisite postoperative disease management creates need for better understanding and new strategies to control the disease. The interaction between genetic and non-genetic factors roots the multifactorial status of this disease, which remains incompletely explored. The small non-coding microRNAs (miRs, miRNAs) regulate several biological processes via post-transcriptional regulation of gene expression. Abnormal expression of miRs in developing and adult heart is associated with anomalous cardiac cell differentiation, cardiac dysfunction, and cardiovascular diseases. Here, we attempt to discover the changes in cardiac miRNA transcriptome in CHD patients over those without CHD (non-CHD) and find its role in CHD through functional annotation. This study explores the miRNome in three most commonly occurring CHD subtypes, namely atrial septal defect (ASD), ventricular septal defect (VSD), and tetralogy of fallot (TOF). We found 295 dysregulated miRNAs through high-throughput sequencing of the cardiac tissues. The bioinformatically predicted targets of these differentially expressed miRs were functionally annotated to know they were entailed in cell signal regulatory pathways, profoundly responsible for cell proliferation, survival, angiogenesis, migration and cell cycle regulation. Selective miRs (hsa-miR-221-3p, hsa-miR-218-5p, hsa-miR-873-5p) whose expression was validated by qRT-PCR, have been reported for cardiogenesis, cardiomyocyte proliferation, cardioprotection and cardiac dysfunction. These results indicate that the altered miRNome to be responsible for the disease status in CHD patients. Our data expand the existing knowledge on the epigenetic changes in CHD. In future, characterization of these cardiac-specific miRs will add huge potential to understand cardiac development, function, and molecular pathogenesis of heart diseases with a prospect of epigenetic manipulation for cardiac repair.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Deep sequencing; Heart; Molecular pathogenesis of CHD; Septal defect; Tetralogy of fallot; miRNA

Mesh:

Substances:

Year:  2022        PMID: 35668131     DOI: 10.1007/s00438-022-01908-z

Source DB:  PubMed          Journal:  Mol Genet Genomics        ISSN: 1617-4623            Impact factor:   2.980


  42 in total

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3.  Cul1 promotes melanoma cell proliferation by promoting DEPTOR degradation and enhancing cap-dependent translation.

Authors:  Lan Chen; Tianyu Liu; Yunhua Tu; Dongyun Rong; Yu Cao
Journal:  Oncol Rep       Date:  2015-11-23       Impact factor: 3.906

4.  Ventricular septal defect and associated complications.

Authors:  Tauseef Asma Chaudhry; Muhammad Younas; Ahsan Baig
Journal:  J Pak Med Assoc       Date:  2011-10       Impact factor: 0.781

5.  Comparison between use of direct oral anticoagulants and aspirin for risk of thromboembolism complications in patients undergoing total knee and hip arthroplasty: a systematic review and meta-analysis.

Authors:  J-Y Cai; C-M Cui; J-K Min; Y-Q Cao; L-Y Zhang
Journal:  Eur Rev Med Pharmacol Sci       Date:  2021-10       Impact factor: 3.507

6.  Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation.

Authors:  Toshiyuki Araki; M Golam Mohi; Fraz A Ismat; Roderick T Bronson; Ifor R Williams; Jeffery L Kutok; Wentian Yang; Lily I Pao; D Gary Gilliland; Jonathan A Epstein; Benjamin G Neel
Journal:  Nat Med       Date:  2004-07-25       Impact factor: 53.440

7.  Genetic association study of APOA1/C3/A4/A5 gene cluster and haplotypes on triglyceride and HDL cholesterol in a community-based population.

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Journal:  Clin Chim Acta       Date:  2007-10-11       Impact factor: 3.786

8.  The cardiac proteome in patients with congenital ventricular septal defect: A comparative study between right atria and right ventricles.

Authors:  A R Bond; D Iacobazzi; S Abdul-Ghani; M T Ghorbel; K J Heesom; S J George; M Caputo; M-S Suleiman; R M Tulloh
Journal:  J Proteomics       Date:  2018-03-20       Impact factor: 4.044

9.  Analysis of circulating microRNAs in patients with repaired Tetralogy of Fallot with and without heart failure.

Authors:  Masood Abu-Halima; Eckart Meese; Andreas Keller; Hashim Abdul-Khaliq; Tanja Rädle-Hurst
Journal:  J Transl Med       Date:  2017-07-10       Impact factor: 5.531

Review 10.  MicroRNAs in Cardiac Diseases.

Authors:  Robin M W Colpaert; Martina Calore
Journal:  Cells       Date:  2019-07-18       Impact factor: 6.600

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