Transcriptome wide changes in long noncoding RNAs in diabetic ischemic heart disease

More than 10% of adults in the United States have type 2 diabetes mellitus (DM) with a 2-4 times higher prevalence of ischemic heart disease than the non-diabetics. Despite extensive research approaches to limit this life-threatening condition have proven unsuccessful, highlighting the need for understanding underlying molecular mechanisms. Long noncoding RNAs (lncRNAs), which regulate gene expression by acting as signals, decoys, guides, or scaffolds have been implicated in diverse cardiovascular conditions. However, their role in ischemic heart disease in DM remains poorly understood. We provide new insights into the lncRNA expression profile after ischemic heart disease in DM mice. We performed unbiased RNA sequencing of well-characterized type 2 DM model db/db mice or its control db/+ subjected to sham or MI surgery. Computational analysis of the RNA sequencing of these LV tissues identified several differentially expressed lncRNAs between (db/db sham vs. db/db MI) including Gm19522 and Gm8075. lncRNA Gm-19522 may regulate DNA replication via DNA protein kinases, while lncRNA Gm-8075 is associated with cancer gene dysregulation and PI3K/Akt pathways. Thus, the downregulation of lncRNAs Gm19522 and Gm8075 post-MI may serve as potential biomarkers or novel therapeutic targets to improve cardiac repair/recovery in diabetic ischemic heart disease.

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Publication Details

Journal
Cardiovascular Diabetology
Published
2024-10-17
DOI
https://doi.org/10.1186/s12933-024-02441-6
Citations
4
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
1.14

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article

Transcriptome wide changes in long noncoding RNAs in diabetic ischemic heart disease

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4 citations
Cardiovascular Diabetology
Cancer-related molecular mechanisms research
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article

Transcriptome wide changes in long noncoding RNAs in diabetic ischemic heart disease

Shizuka Uchida, Noemi Nisini, Malik Bisserier, Rajika Roy, Amit Kumar, Rajesh Katare, David A. Goukassian, Michela Piedepalumbo, Tiffany Lee, Konstantinos Drosatos, Venkata Naga Srikanth Garikipati, Claudio de Lucia, Ioannis D. Kyriazis, Natarajaseenivasan Suriya Muthukumaran, Raj Kishore
article en
4 citations

Abstract

More than 10% of adults in the United States have type 2 diabetes mellitus (DM) with a 2-4 times higher prevalence of ischemic heart disease than the non-diabetics. Despite extensive research approaches to limit this life-threatening condition have proven unsuccessful, highlighting the need for understanding underlying molecular mechanisms. Long noncoding RNAs (lncRNAs), which regulate gene expression by acting as signals, decoys, guides, or scaffolds have been implicated in diverse cardiovascular conditions. However, their role in ischemic heart disease in DM remains poorly understood. We provide new insights into the lncRNA expression profile after ischemic heart disease in DM mice. We performed unbiased RNA sequencing of well-characterized type 2 DM model db/db mice or its control db/+ subjected to sham or MI surgery. Computational analysis of the RNA sequencing of these LV tissues identified several differentially expressed lncRNAs between (db/db sham vs. db/db MI) including Gm19522 and Gm8075. lncRNA Gm-19522 may regulate DNA replication via DNA protein kinases, while lncRNA Gm-8075 is associated with cancer gene dysregulation and PI3K/Akt pathways. Thus, the downregulation of lncRNAs Gm19522 and Gm8075 post-MI may serve as potential biomarkers or novel therapeutic targets to improve cardiac repair/recovery in diabetic ischemic heart disease.

Cardiovascular DiabetologyVol. 23(1)
University of Thessaly (GR), Duke University (US), New York Medical College (US), ASL Roma (IT), Azienda Sanitaria Locale Roma 3 (IT), University of Cincinnati (US), University of Otago (NZ), Temple University (US), Aalborg University (DK), University of Cincinnati Medical Center (US), Icahn School of Medicine at Mount Sinai (US)
American Heart Association, Temple University, National Institutes of Health, National Heart, Lung, and Blood Institute
Good health and well-being
Openalex Percentile: Top 21%
Cancer-related molecular mechanisms research
1.14
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