Coordinating Regulation of Gene Expression in Cardiovascular Disease

A special issue of Genes (ISSN 2073-4425). This special issue belongs to the section "Human Genomics and Genetic Diseases".

Deadline for manuscript submissions: 10 April 2026 | Viewed by 5

Special Issue Editor


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Guest Editor
1 Center for Cutaneous Biology and Immunology Research, Department of Dermatology, Henry Ford Health, Detroit, MI, USA
2 Immunology Research Program, Henry Ford Cancer Institute, Henry Ford Health, Detroit, MI, USA
Interests: gene; MicroRNA; cardiovascular disease;chronic obstructive pulmonary disease; reactive oxygen species; pulmonary hypertension; oxidative stress

Special Issue Information

Dear Colleagues,

Cardiovascular disease (CVD) is the leading cause of death globally and encompasses a wide range of conditions, including coronary artery disease, heart failure, arrhythmias, and vascular disorders. While the genetic basis of many cardiovascular disorders has been well established, there is a growing appreciation that regulatory mechanisms governing gene expression—both at the transcriptional and post-transcriptional levels—play an equally critical role in determining disease onset, progression, and therapeutic response.

This Special Issue aims to explore the complex regulatory networks that coordinate gene expression in cardiovascular health and disease. Gene regulation in cardiac and vascular cells is a highly dynamic process influenced by a multitude of factors: transcription factors, chromatin state, DNA methylation, non-coding RNAs, RNA-binding proteins, and epigenetic modulators. These mechanisms do not operate in isolation; rather, they form intricate and interconnected systems that adapt cellular behavior in response to physiological signals, stress, injury, and environmental exposures.

Recent advances in high-throughput sequencing technologies, single-cell omics, genome editing, and computational biology have enabled researchers to dissect these regulatory layers with unprecedented resolution. These discoveries are uncovering novel therapeutic targets, disease biomarkers, and molecular pathways that can be manipulated to prevent or reverse cardiovascular dysfunction.

This Special Issue invites original research articles, reviews, perspectives, and methodological papers that advance our understanding of how gene expression is regulated and coordinated in the cardiovascular system. Contributions that integrate experimental and computational approaches, or that bridge basic science with clinical relevance, are particularly encouraged.

We welcome submissions exploring a wide range of topics relevant to gene expression regulation in cardiovascular disease, including but not limited to the following:

  • Transcriptional control of cardiac development, remodeling, and failure;
  • Epigenetic regulation (DNA methylation, histone modifications, chromatin architecture) in cardiac and vascular cells;
  • Role of non-coding RNAs (microRNAs, lncRNAs, circRNAs) in regulating gene expression during CVD;
  • Post-transcriptional mechanisms (alternative splicing, RNA editing, RNA-binding proteins);
  • Single-cell and spatial transcriptomics to map gene expression in diseased tissues;
  • Gene-environment interactions and their impact on cardiovascular gene regulation;
  • Sex- and age-specific differences in gene expression networks;
  • Therapeutic modulation of gene expression using small molecules, RNA therapeutics, or CRISPR-based tools;
  • Bioinformatics and systems biology approaches to decipher regulatory networks;
  • Clinical implications of gene regulation studies in diagnosis, risk stratification, and treatment of CVD.

Dr. Nirmal Parajuli
Guest Editor

Manuscript Submission Information

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Keywords

  • microRNA
  • oxidative stress
  • cardiovascular disease
  • chronic obstructive pulmonary disease (COPD)
  • pulmonary hypertension
  • gene regulation
  • inflammation
  • reactive oxygen species (ROS)
  • molecular biomarkers
  • precision medicine

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Published Papers

This special issue is now open for submission.
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