Mycophenolate Mofetil Inhibits Ferroptosis by Boosting Autophagy to Prevent Pulmonary Fibrosis DOI
Weili Liu, Bo Liu, Hongbo Li

et al.

Published: Jan. 1, 2025

Language: Английский

piR112710 attenuates diabetic cardiomyopathy through inhibiting Txnip/NLRP3-mediated pyroptosis in db/db mice DOI

Ande Jiao,

Huaxing Liu, Huihui Wang

et al.

Cellular Signalling, Journal Year: 2024, Volume and Issue: 122, P. 111333 - 111333

Published: Aug. 3, 2024

Language: Английский

Citations

6

Engineering circular RNA medicines DOI
Xiaofei Cao,

Zhengyi Cai,

Jinyang Zhang

et al.

Nature Reviews Bioengineering, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 20, 2024

Language: Английский

Citations

6

Expanding roles of circRNAs in cardiovascular diseases DOI Creative Commons
Xu Liu, Xuelin Yao, Liang Chen

et al.

Non-coding RNA Research, Journal Year: 2024, Volume and Issue: 9(2), P. 429 - 436

Published: Feb. 5, 2024

CircRNAs are a class of single-stranded RNAs characterized by covalently looped structures. Emerging advances have promoted our understanding circRNA biogenesis, nuclear export, biological functions, and functional mechanisms. Roles circRNAs in diverse diseases been increasingly recognized the past decade, with novel approaches bioinformatics analysis new strategies modulating levels, which made hot spot for therapeutic applications. Moreover, due to intrinsic features such as high stability, conservation, tissue-/stage-specific expression, believed be promising prognostic diagnostic markers diseases. Aiming cardiovascular disease (CVD), one leading causes mortality worldwide, we briefly summarize current circRNAs, provide recent progress functions mechanisms CVD, discuss future perspectives both research therapeutics based on existing knowledge.

Language: Английский

Citations

5

Salvianolic acid B ameliorates myocardial fibrosis in diabetic cardiomyopathy by deubiquitinating Smad7 DOI Creative Commons
Hong Luo,

Lingyun Fu,

Xueting Wang

et al.

Chinese Medicine, Journal Year: 2023, Volume and Issue: 18(1)

Published: Dec. 10, 2023

Salvianolic acid B (Sal B), a water-soluble phenolic compound derived from Salvia miltiorrhiza Bunge, is commonly used in Traditional Chinese Medicine to treat cardiovascular disease. In our previous study, Sal protected against myocardial fibrosis induced by diabetic cardiomyopathy (DCM). This study aimed investigate the ameliorative effects and potential mechanisms of mitigating DCM.Various methods were on DCM vivo vitro. These included blood glucose measurement, echocardiography, HE staining, Masson's trichrome Sirius red cell proliferation assessment, determination hydroxyproline levels, immunohistochemical evaluation fibrosis-related protein expression (Collagen-I, Collagen-III, TGF-β1, p-Smad3, Smad3, Smad7, α-smooth muscle actin), analysis Smad7 gene expression, ubiquitin modification.The animal test results indicated that significantly improved cardiac function, inhibited collagen deposition phenotypic transformation, ameliorated upregulating thereby inhibiting TGF-β1 signaling pathway. addition, experiments demonstrated proliferation, migration, secretion fibroblasts (CFs) high (HG). decreased ubiquitination stabilized increasing CFs pathway, which may be mechanism mitigates DCM.This revealed can improve deubiquitinating stabilizing blocking

Language: Английский

Citations

12

Ferroptosis in cardiovascular diseases: role and mechanism DOI Creative Commons
Qi Zhang, Yuhao Luo, Peng Lin

et al.

Cell & Bioscience, Journal Year: 2023, Volume and Issue: 13(1)

Published: Dec. 15, 2023

Abstract In multicellular organisms, regulatory cell death is a crucial aspect of growth and development. Ferroptosis, which was postulated roughly ten years ago, mode that differs from apoptosis, autophagy, pyrodeath. This distinct pattern triggered by an imbalance between oxidants antioxidants strongly associated with the metabolism iron, lipids, amino acids, glutathione. A growing body research has implicated ferroptosis in incidence progression many organ traumas degenerative diseases. Recently, gained attention as mechanism underlying initiation development variety cardiovascular diseases, including myocardial ischemia/reperfusion injury, cardiomyopathy, arrhythmia, chemotherapy, Corona Virus-2-induced cardiac injury. Pharmacological therapies inhibit have great potential for management disorders. review discusses prevalence mechanisms ferroptosis, effect on immune system, significance therapeutic value regulating heart

Language: Английский

Citations

11

The role of ncRNAs‐mediated pyroptosis in diabetes and its vascular complications DOI
Xinyao Feng, Xiaoxu Yang,

Yancheng Zhong

et al.

Cell Biochemistry and Function, Journal Year: 2024, Volume and Issue: 42(2)

Published: March 1, 2024

Abstract Over the past decade, prevalence of diabetes has increased significantly worldwide, leading to an increase in vascular complications (VCD), such as diabetic cardiomyopathy (DCM), nephropathy (DN), and retinopathy (DR). Noncoding RNAs (ncRNAs), microRNAs (miRNAs), long (lncRNAs), circular (circRNAs), play a key role cellular processes, including pathophysiology VCD via pyroptosis. ncRNAs (e.g., miR‐17, lnc‐MEG3, lnc‐KCNQ1OT1) can regulate pyroptosis pancreatic β cells. Some are involved progression. For example, miR‐21, lnc‐KCNQ1OT1, lnc‐GAS5, lnc‐MALAT1 were reported DN DCM, lnc‐MIAT was identified DCM DR. Herein, this review aimed summarize recent research findings related ncRNAs‐mediated at onset progression VCD.

Language: Английский

Citations

4

New insights into the roles of Irisin in diabetic cardiomyopathy and vascular diseases DOI Open Access
Tiandong Zhang, Yi Qian,

Wenhua Huang

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 175, P. 116631 - 116631

Published: April 25, 2024

Diabetes mellitus (DM) is a prevalent chronic disease in the 21st century due to increased lifespan and unhealthy lifestyle choices. Extensive research indicates that exercise can play significant role regulating systemic metabolism by improving energy mitigating various metabolic disorders, including DM. Irisin, well-known exerkine, was initially reported enhance expenditure indicating browning of white adipose tissue (WAT) through peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) signaling. In this review, we summarize potential mechanisms underlying beneficial effects Irisin on glucose dysmetabolism, reducing gluconeogenesis, enhancing insulin expenditure, promoting glycogenesis. Additionally, highlight Irisin's improve diabetic vascular diseases stimulating nitric oxide (NO) production, oxidative nitrosative stress, curbing inflammation, attenuating endothelial cell aging. Furthermore, discuss cardiomyopathy preventing cardiomyocyte loss myocardial hypertrophy fibrosis. Given promising functions managing diseases, targeting for therapeutic purposes could be fruitful avenue future clinical interventions.

Language: Английский

Citations

4

Clinical Significance and Potential Mechanism of Circ_00008842 in Acute Myocardial Infarction DOI Open Access

Li Zhang,

Ming Wang, Ran Liao

et al.

International Heart Journal, Journal Year: 2024, Volume and Issue: 65(4), P. 703 - 712

Published: July 12, 2024

This study aimed to evaluate the clinical value of circ_0008842 in acute myocardial infarction (AMI) and explore potential mechanisms.GSE149051 GSE160717 datasets analyze common differentially expressed circRNAs (coDEcircRNA) AMI. RT-qPCR analysis mRNA levels patients with ROC curve assesses diagnostic A cell model AMI was constructed by hypoxia-reoxygenation (H/R) -induced H9c2. Cell viability apoptosis were examined CCK-8 flow cytometry. Enzyme-linked immunosorbent assay used injury markers CK-MB cTnI secretion. Dual luciferase reporter assays validate binding miRNA. PPI network gene ontology Kyoto Encyclopedia Genes Genomes pathway enrichment reveal functions pathways targets from miRNA AMI.circ_0008842 is recognized as coDEcircRNA AMI-related databases. greatly lower miR-574-5p significantly higher than healthy individuals. a target circ_0008842. The sensitivity specificity for diagnosing 87.40% 83.50%, respectively. Overexpression inhibited H/R induced apoptosis, increased viability, decreased levels, which partially abrogated overexpression miR-574-5p. Calmodulin-like protein 4 (CALML4) most connected hub predicted genes.circ_0008842 biomarker participates regulating Our provides new insights into diagnosis

Language: Английский

Citations

4

Circ-0006332 stimulates cardiomyocyte pyroptosis via the miR-143/TLR2 axis to promote doxorubicin-induced cardiac damage DOI Creative Commons
Ping Zhang, Yuanyuan Liu,

Yuliang Zhan

et al.

Epigenetics, Journal Year: 2024, Volume and Issue: 19(1)

Published: July 17, 2024

Doxorubicin (DOX)-mediated cardiotoxicity can impair the clinical efficacy of chemotherapy, leading to heart failure (HF). Given importance circRNAs and miRNAs in HF, this paper intended delineate mechanism circular RNA 0006332 (circ -0,006,332)/microRNA (miR)-143/Toll-like receptor 2 (TLR2) axis doxorubicin (DOX)-induced HF. The binding miR-143 circ -0,006,332 TLR2 was assessed with dual-luciferase assay, between determined FISH, RIP, pull-down assays. and/or were overexpressed rats cardiomyocytes, followed by DOX treatment. In expression, cell viability, LDH release, ATP contents, levels IL-1β, IL-18, TNF-α, pyroptosis-related molecules examined. rats, cardiac function, serum enzymes, apoptosis, myocardial fibrosis, TLR2, detected. diminished expression bound downregulate expression. reduced augmented DOX-induced cardiomyocytes. inhibited cytotoxicity suppressing pyroptosis H9C2 dysfunction, levels, pyroptosis. Furthermore, overexpression blocked these effects on cardiomyocytes rats. Circ stimulates cardiomyocyte downregulating upregulating thus promoting injury.

Language: Английский

Citations

4

[The splicing factor HNRNPH1 regulates Circ-MYOCD back-splicing to modulate the course of cardiac hypertrophy]. DOI
Rui Cai, Zhuo Huang, Wenxia He

et al.

PubMed, Journal Year: 2025, Volume and Issue: 45(3), P. 587 - 594

Published: March 20, 2025

To explore the mechanism of Circ-MYOCD back-splicing and its regulatory role in myocardial hypertrophy. Sanger sequencing RNase R assays were performed to verify circularity stability Circ-MYOCD, whose subcellular distribution was determined by nuclear-cytoplasmic fractionation. Bioinformatics analysis mass spectrometry from pull-down conducted predict RNA-binding proteins (RBPs) interacting with Circ-MYOCD. In rat cardiomyocytes H9C2 cells, effects HNRNPH1 HNRNPL knockdown overexpression on evaluated. a cell model angiotensin II (Ang II)-induced hypertrophy, expression detected, progression hypertrophy assessed, effect analyzed. confirmed that junction primers could amplify correct sequence. fractionation showed stable predominantly localized cytoplasm. assay identified as RBPs significantly enhanced while inhibited back-splicing; obviously increased expressions markers ANP BNP, produced opposite effect. Ang II-induced which exhibited significant increase expression, decreased MYOCD lowered both BNP expressions. regulates influence

Language: Английский

Citations

0