Khidr Emad Gamil, Abulsoud Ahmed I, Doghish Ayman A, El-Mahdy Hesham A, Ismail Ahmed, Elballal Mohammed S, Sarhan Omnia M, Abdel Mageed Sherif S, Elsakka Elsayed G E, Elkhawaga Samy Y, El-Husseiny Ahmed A, Abdelmaksoud Nourhan M, El-Demerdash Aya A, Shahin Reem K, Midan Heba M, Elrebehy Mahmoud A, Mohammed Osama A, Abulsoud Logyna A, Doghish Ahmed S
Biochemistry and Molecular Biology Department, Faculty of Pharmacy (Boys), Al-Azhar University, Nasr City 11231, Cairo, Egypt.
Biochemistry and Molecular Biology Department, Faculty of Pharmacy (Boys), Al-Azhar University, Nasr City 11231, Cairo, Egypt; Biochemistry Department, Faculty of Pharmacy, Heliopolis University, Cairo 11785, Egypt.
Pathol Res Pract. 2023 Aug;248:154624. doi: 10.1016/j.prp.2023.154624. Epub 2023 Jun 17.
For the past two decades since their discovery, scientists have linked microRNAs (miRNAs) to posttranscriptional regulation of gene expression in critical cardiac physiological and pathological processes. Multiple non-coding RNA species regulate cardiac muscle phenotypes to stabilize cardiac homeostasis. Different cardiac pathological conditions, including arrhythmia, myocardial infarction, and hypertrophy, are modulated by non-coding RNAs in response to stress or other pathological conditions. Besides, miRNAs are implicated in several modulatory signaling pathways of cardiovascular disorders including mitogen-activated protein kinase, nuclear factor kappa beta, protein kinase B (AKT), NOD-like receptor family pyrin domain-containing 3 (NLRP3), Jun N-terminal kinases (JNKs), Toll-like receptors (TLRs) and apoptotic protease-activating factor 1 (Apaf-1)/caspases. This review highlights the potential role of miRNAs as therapeutic targets and updates our understanding of their roles in the processes underlying pathogenic phenotypes of cardiac muscle.
自发现以来的过去二十年里,科学家们已将微小RNA(miRNA)与关键心脏生理和病理过程中基因表达的转录后调控联系起来。多种非编码RNA物种调节心肌表型以稳定心脏内环境稳态。不同的心脏病理状况,包括心律失常、心肌梗死和肥大,会受到非编码RNA的调节,以应对压力或其他病理状况。此外,miRNA参与心血管疾病的多种调节信号通路,包括丝裂原活化蛋白激酶、核因子κB、蛋白激酶B(AKT)、含NOD样受体家族吡啉结构域3(NLRP3)、Jun氨基末端激酶(JNK)、Toll样受体(TLR)以及凋亡蛋白酶激活因子1(Apaf-1)/半胱天冬酶。本综述强调了miRNA作为治疗靶点的潜在作用,并更新了我们对其在心肌致病表型潜在机制中作用的理解。