Evidence map›Paper›PMID 39420368›Full record

ArticleCardiovascular diabetology2024

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

Amit Kumar Rai, Natarajaseenivasan Suriya Muthukumaran, Noemi Nisini, Tiffany Lee, Ioannis D Kyriazis, Claudio de Lucia, Michela Piedepalumbo, Rajika Roy, Shizuka Uchida, Konstantinos Drosatos and 5 more

Abstract read
In one paragraph

Article in Cardiovascular diabetology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Amit Kumar RaiAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Natarajaseenivasan Suriya MuthukumaranAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Noemi NisiniAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Tiffany LeeAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Ioannis D KyriazisAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Claudio de LuciaAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Michela PiedepalumboAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Rajika RoyAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Shizuka UchidaDepartment of Clinical Medicine, Center for RNA Medicine, Aalborg University, Frederikskaj 10B, 2. (Building C), Copenhagen SV, 2450, Denmark.
Konstantinos DrosatosMetabolic Biology Laboratory, Department of Pharmacology and Systems Physiology, Cardiovascular Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Malik BisserierDepartment of Cell Biology and Anatomy and Physiology, New York Medical College, Valhalla, NY, USA.
Rajesh KatareDepartment of Physiology, HeartOtago, School of Biomedical Sciences, University of Otago, Dunedin, New Zealand.
David GoukassianCardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, USA.
Raj KishoreAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA.
Venkata Naga Srikanth GarikipatiAging + Cardiovascular Discovery Center, Lewis Katz School of Medicine, Temple University, Philadelphia, 19140, USA. venkata.naga.srikanth.garikipati@temple.edu.

Funding

Promoting Academic Workforce Development in Behavioral Medicine and Sleep Disorders ResearchR25HL105444 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Girardin Jean-Louis, Tatjana Rundek · 2010 to 2026
$5.8M
PRIDE Academy: Impact of Ancestry and Gender to omics of lung diseasesR25HL146166 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI Matthew Wayne DeCamp, Sonia Castro Flores · 2019 to 2026
$3.4M
Restoration of myocardial reparative function of diabetic progenitor cells by epigenetic modulationR01HL143892 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KISHORE, RAJ · 2020 to 2023
$2.2M
Role of small RNAs in ischemic tissue repairR01HL164794 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI Venkata Naga Srikanth Garikipati · 2023 to 2026
$2.2M
Role of SIN3a in the epigenetic regulation of the Bone Morphogenetic Protein Receptor Type 2 in pulmonary arterial hypertensionK01HL159038 · NHLBI · NEW YORK MEDICAL COLLEGE · PI BISSERIER, MALIK · 2022 to 2024
$406k
American Heart Association Career Development Award 24CDA1269532American Heart Association Innovative Project Award 23IPA105444American Heart Association Post Doctoral Fellowship grant 2021AHA000POST000217114NHLBI NIH HHS K01 HL159038NHLBI NIH HHS R01 HL143892NHLBI NIH HHS R01 HL164794NHLBI NIH HHS R25 HL146166NIH HHS 1K01HL159038-01A1NIH HHS 5R25HL146166NIH HHS HL143892NIH HHS R01 grant HL164794
6 · The paper itself

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.

Indexed as

Diabetes Mellitus, Type 2Disease Models, AnimalGene Expression ProfilingMyocardial IschemiaRNA, Long NoncodingTranscriptomeAnimalsDiabetic CardiomyopathiesGene Expression RegulationMaleMiceMice, Inbred C57BLMyocardial InfarctionMyocardiumSignal TransductionRNA, Long NoncodingDb/db miceDiabetesIschemic heart diseaseLong noncoding RNATranscriptome

Identifiers

PMID39420368
PMCPMC11488282

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.