Long non‑coding RNA PEG13 regulates endothelial cell senescence through the microRNA‑195/IRS1 axis DOI Open Access
Qin Huang,

Haiwen Zhou,

Songping Yu

и другие.

Experimental and Therapeutic Medicine, Год журнала: 2023, Номер 26(6)

Опубликована: Ноя. 3, 2023

Atherosclerosis is a chronic inflammatory disease characterized by endothelial dysfunction and plaque formation. The present study aimed to elucidate the pathological role of long non-coding RNA (lncRNA) paternally expressed 13 (PEG13) in onset progression atherosclerosis. Specifically, its effects on human umbilical vein cell (HUVEC) proliferation, angiogenesis, senescence senescence-associated secretory phenotype (SASP)-related factors were investigated using cellular β-galactosidase staining, reverse transcription-quantitative PCR enzyme-linked immunosorbent assays. results showed that oxidized low-density lipoprotein (ox-LDL) inhibited lncRNA PEG13 expression HUVEC viability dose-dependent manner overexpression partially reversed these effects. Additionally, ameliorated ox-LDL-induced impairment SASP. Furthermore, directly targeted microRNA (miR/miRNA)-195-5p, suppressing upregulation miRNA. gene coding for insulin receptor substrate 1 (IRS1), an activator phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) signaling pathway, was confirmed as direct target miR-195. attenuated inhibition IRS1 PI3K/AKT protective viability, angiogenesis small interfering RNAs targeting IRS1. demonstrated attenuates HUVECs modulating miR-195/IRS1/PI3K/AKT suggesting potential therapeutic treatment

Язык: Английский

Expression of HMGB1, TGF-β1, BIRC3, ADAM17, CDKN1A, and FTO in Relation to Left Ventricular Remodeling in Patients Six Months after the First Myocardial Infarction: A Prospective Study DOI Open Access
Jovana Kuveljić, Ana Djordjević, Ivan Životić

и другие.

Genes, Год журнала: 2024, Номер 15(10), С. 1296 - 1296

Опубликована: Окт. 2, 2024

After myocardial infarction (MI), adverse left ventricular (LV) remodeling may occur. This is followed by LV hypertrophy and eventually heart failure. The process complex goes through multiple phases. aim of this study was to investigate the expression

Язык: Английский

Процитировано

1

Bibliometric analysis of youth myocardial infarction research (1980–2023) DOI Creative Commons
Yang Fu, Qi Han, Fei Wang

и другие.

Frontiers in Cardiovascular Medicine, Год журнала: 2024, Номер 11

Опубликована: Ноя. 26, 2024

Cardiovascular diseases include myocardial infarction, a high mortality disease. Myocardial infarction patients are becoming younger, typically defined as under 45 years of age. This study analyzes the relevant papers on in youth Web Science Core Collection (WoSCC) between 1980 and 2023.

Язык: Английский

Процитировано

1

Cardiac cells and mesenchymal stem cells derived extracellular vesicles: a potential therapeutic strategy for myocardial infarction DOI Creative Commons

Dan Qin,

Xiaobo Wang, Jun Pu

и другие.

Frontiers in Cardiovascular Medicine, Год журнала: 2024, Номер 11

Опубликована: Дек. 18, 2024

Despite improvements in clinical outcomes of acute myocardial infarction (AMI), mortality rates remain high, indicating the need for further understanding pathogenesis and developing more effective cardiac protection strategies. Extracellular vesicles (EVs) carry proteins noncoding RNAs (ncRNAs) derived from different cell populations, mainly including cardiomyocytes, endothelial cells, progenitor cardiosphere-derived immune fibroblasts telocytes have vital roles under both physiological pathological process such as (MI). The content EVs can also indicate status their parental cells serve a biomarker monitoring risk injury. Examining these offer fresh perspectives on development MI assist creating innovative treatments. Additionally, mesenchymal stem (MSCs) (MSC-EVs) been shown to significant potential regeneration. In this review, we will discuss current role communication, with focus various MSCs uses therapies after MI.

Язык: Английский

Процитировано

1

Integrative analyses and validation of ferroptosis-related genes and mechanisms associated with cerebrovascular and cardiovascular ischemic diseases DOI Creative Commons
Wei Liao,

Yuehui Wen,

Chuan Zeng

и другие.

BMC Genomics, Год журнала: 2023, Номер 24(1)

Опубликована: Дек. 4, 2023

There has been a gradual increase in the occurrence of cardiovascular and cerebrovascular ischemic diseases, particularly as comorbidities. Yet, mechanisms underlying these diseases remain unclear. Ferroptosis emerged potential contributor to cardio-cerebral processes. Therefore, this study investigated shared biological between two processes, well role ferroptosis genes damage, by constructing co-expression modules for myocardial ischemia (MI) stroke (IS) network protein-protein interactions, mRNA-miRNA, mRNA-transcription factors (TFs), mRNA-RNA-binding proteins (RBPs), mRNA-drug interactions.The identified seven key genes, specifically ACSL1, TLR4, ADIPOR1, G0S2, PDK4, HP, PTGS2, subjected them functional enrichment analysis during ischemia. The predicted miRNAs were found interact with 35 hub interactions observed 11 30 TF transcription factors. Additionally, 10 RBPs corresponding 16 163 molecular compounds identified. This also clarified levels immune infiltration MI IS different subtypes. Finally, we four including using diagnostic model constructed Least Absolute Shrinkage Selection Operator (LASSO) regression analysis; HP shown have value co-pathogenesis cerebral both validation test data RT-qPCR assay.To best our knowledge, is first utilize multiple algorithms comprehensively analyze processes from various perspectives. proven valuable offering insights investigation injury pathways injuries. may serve markers diseases.

Язык: Английский

Процитировано

2

Ispinesib Mesylate-induced oxidative stress via miR-30e-5p/BCL2L11 axis in acute myocardial infarction: a comprehensive bioinformatics and experimental validation investigation DOI Creative Commons

Wu Ningxia,

Fei Li

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Авг. 1, 2024

Abstract Objective Cardiovascular disorders constitute a substantial threat to global human health and safety. Of note, acute myocardial infarction (AMI), being grave cardiovascular disorder, has garnered considerable attention owing its elevated prevalence, mortality broad demographic distribution. It is well established that hypoxia-induced apoptosis significantly contributes towards the onset progression of AMI; however, several aspects regarding biological indicators molecular mechanisms AMI remain elusive. Method This investigation utilized Gene Expression Comprehensive (GEO) database perform comprehensive analysis pivotal genes employing techniques like differential analysis, Venn weighted correlation network (WGCNA). Subsequently, between key factors was scrutinized, potential causal link these outcome probed via Mendelian randomization (MR). Additionally, real-time quantitative polymerase chain reaction (RT-qPCR) lentivirus transfection experiments were executed, miRNA-mRNA networks constructed utilizing miRBase databases, three-dimensional structures predicted with aid RNAfold Vfold3D drug sensitivity conducted using RNAactDrug databases. Result Following classification, WGCNA clustering, Wien screening two distinctly expressed intimately linked - PTEN BCL2L11 successfully identified. The outcomes RT-qPCR infection corroborated expression pattern conformed our prior findings. unveiled robust relationship single nucleotide polymorphisms (SNPs) AMI. Lastly, through susceptibility it discerned Ispinesib Mesylate, Bleomycin (50 uM)/miR-141-3p/BCL2L11 axis could potentially serve as efficacious therapeutic or preventive strategies against Conclusion In this study, we introduced novel concepts Mesylate axis, offering fresh perspective on apoptotic mechanism in

Язык: Английский

Процитировано

0

GENE MARKERS IDENTIFICATION OF ACUTE MYOCARDIAL INFARCTION DISEASE BASED ON GENOMIC PROFILING THROUGH EXTREME GRADIENT BOOSTING (XGBoost) DOI Creative Commons
Rohmatul Fajriyah,

Havidzah Asri Isnandar,

Adhar Arifuddin

и другие.

MEDIA STATISTIKA, Год журнала: 2024, Номер 17(1), С. 69 - 80

Опубликована: Окт. 13, 2024

One disease that can cause death is Acute Myocardial Infarction (AMI). AMI, also known as a heart attack, condition causes permanent damage to muscle tissue due prolonged ischemia or lack of blood flow occurs blockage the epicardial coronary arteries and results in clots limiting supply myocardium. During years young AMI patients are increasing. ways diagnose early providing information biomarkers related this by implementing bioinformatics data analysis. The research was conducted look at genomic profile suffering from based on without recurrent events normal control, using XGBoost method, its scalability efficiency. Based grid search tuning hyperparameters, method gives classification accuracy 88.89%, AUC 90 kappa 0.7805. These indicate classify well. This has identified three genes contribute most classifying patients, namely calponin 2, ribosomal protein S11 myotropin. heatmap visualization, obtained class markers events.

Язык: Английский

Процитировано

0

Long non‑coding RNA PEG13 regulates endothelial cell senescence through the microRNA‑195/IRS1 axis DOI Open Access
Qin Huang,

Haiwen Zhou,

Songping Yu

и другие.

Experimental and Therapeutic Medicine, Год журнала: 2023, Номер 26(6)

Опубликована: Ноя. 3, 2023

Atherosclerosis is a chronic inflammatory disease characterized by endothelial dysfunction and plaque formation. The present study aimed to elucidate the pathological role of long non-coding RNA (lncRNA) paternally expressed 13 (PEG13) in onset progression atherosclerosis. Specifically, its effects on human umbilical vein cell (HUVEC) proliferation, angiogenesis, senescence senescence-associated secretory phenotype (SASP)-related factors were investigated using cellular β-galactosidase staining, reverse transcription-quantitative PCR enzyme-linked immunosorbent assays. results showed that oxidized low-density lipoprotein (ox-LDL) inhibited lncRNA PEG13 expression HUVEC viability dose-dependent manner overexpression partially reversed these effects. Additionally, ameliorated ox-LDL-induced impairment SASP. Furthermore, directly targeted microRNA (miR/miRNA)-195-5p, suppressing upregulation miRNA. gene coding for insulin receptor substrate 1 (IRS1), an activator phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) signaling pathway, was confirmed as direct target miR-195. attenuated inhibition IRS1 PI3K/AKT protective viability, angiogenesis small interfering RNAs targeting IRS1. demonstrated attenuates HUVECs modulating miR-195/IRS1/PI3K/AKT suggesting potential therapeutic treatment

Язык: Английский

Процитировано

1