Mulvey John F, Meyer Emily L, Svenningsen Mikkel Skjoldan, Lundby Alicia
Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Curr Cardiol Rep. 2025 Mar 21;27(1):74. doi: 10.1007/s11886-025-02226-7.
Despite significant efforts to understand pathophysiological processes underlying cardiac diseases, the molecular causes for the most part remain unresolved. Rapid advancements in -omics technologies, and their application in cardiac research, offer new insight into cardiac remodeling in disease states. This review aims to provide an accessible overview of recent advances in omics approaches for studying cardiac remodeling, catering to readers without extensive prior expertise.
We provide a methodologically focused overview of current methods for performing transcriptomics and proteomics, including their extensions for single-cell and spatial measurements. We discuss approaches to integrate data across modalities, resolutions and time. Key recent applications within the cardiac field are highlighted. Each -omics modality can provide insight, yet each existing experimental method has technical or conceptual limitations. Integrating data across multiple modalities can leverage strengths and mitigate weaknesses, ultimately enhancing our understanding of cardiac pathophysiology.
尽管人们为了解心脏病背后的病理生理过程付出了巨大努力,但大多数分子病因仍未得到解决。组学技术的迅速发展及其在心脏研究中的应用,为疾病状态下的心脏重塑提供了新的见解。本综述旨在为研究心脏重塑的组学方法的最新进展提供一个易于理解的概述,以满足没有广泛专业知识的读者的需求。
我们提供了一个以方法为重点的当前转录组学和蛋白质组学方法概述,包括它们在单细胞和空间测量方面的扩展。我们讨论了跨模态、分辨率和时间整合数据的方法。重点介绍了心脏领域最近的关键应用。每种组学方式都能提供见解,但现有的每种实验方法都有技术或概念上的局限性。跨多种模态整合数据可以发挥优势并减轻弱点,最终增强我们对心脏病理生理学的理解。