Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, Illinois, USA; University of Illinois Cancer Center, Chicago, Illinois, USA.
Mol Cell Proteomics. 2023 Apr;22(4):100528. doi: 10.1016/j.mcpro.2023.100528. Epub 2023 Mar 12.
The extracellular matrix (ECM) is a complex assembly of hundreds of proteins forming the architectural scaffold of multicellular organisms. In addition to its structural role, the ECM conveys signals orchestrating cellular phenotypes. Alterations of ECM composition, abundance, structure, or mechanics have been linked to diseases and disorders affecting all physiological systems, including fibrosis and cancer. Deciphering the protein composition of the ECM and how it changes in pathophysiological contexts is thus the first step toward understanding the roles of the ECM in health and disease and toward the development of therapeutic strategies to correct disease-causing ECM alterations. Potentially, the ECM also represents a vast, yet untapped reservoir of disease biomarkers. ECM proteins are characterized by unique biochemical properties that have hindered their study: they are large, heavily and uniquely posttranslationally modified, and highly insoluble. Overcoming these challenges, we and others have devised mass-spectrometry-based proteomic approaches to define the ECM composition, or "matrisome," of tissues. This first part of this review provides a historical overview of ECM proteomics research and presents the latest advances that now allow the profiling of the ECM of healthy and diseased tissues. The second part highlights recent examples illustrating how ECM proteomics has emerged as a powerful discovery pipeline to identify prognostic cancer biomarkers. The third part discusses remaining challenges limiting our ability to translate findings to clinical application and proposes approaches to overcome them. Lastly, the review introduces readers to resources available to facilitate the interpretation of ECM proteomics datasets. The ECM was once thought to be impenetrable. Mass spectrometry-based proteomics has proven to be a powerful tool to decode the ECM. In light of the progress made over the past decade, there are reasons to believe that the in-depth exploration of the matrisome is within reach and that we may soon witness the first translational application of ECM proteomics.
细胞外基质 (ECM) 是由数百种蛋白质组成的复杂集合体,构成了多细胞生物的结构支架。除了其结构作用外,ECM 还传递信号,协调细胞表型。ECM 组成、丰度、结构或力学的改变与影响所有生理系统的疾病和障碍有关,包括纤维化和癌症。因此,破译 ECM 的蛋白质组成及其在病理生理环境中的变化是理解 ECM 在健康和疾病中的作用以及开发纠正导致疾病的 ECM 改变的治疗策略的第一步。潜在地,ECM 也代表了一个巨大的、尚未开发的疾病生物标志物库。ECM 蛋白具有独特的生化特性,这阻碍了它们的研究:它们体积大、高度和独特的翻译后修饰、高度不溶。为了克服这些挑战,我们和其他研究人员设计了基于质谱的蛋白质组学方法来定义组织的 ECM 组成,即“基质组”。这篇综述的第一部分提供了 ECM 蛋白质组学研究的历史概述,并介绍了最新的进展,这些进展现在允许对健康和患病组织的 ECM 进行分析。第二部分重点介绍了最近的一些例子,说明了 ECM 蛋白质组学如何成为识别预后癌症生物标志物的强大发现途径。第三部分讨论了限制我们将发现转化为临床应用的能力的剩余挑战,并提出了克服这些挑战的方法。最后,该综述向读者介绍了有助于解释 ECM 蛋白质组学数据集的资源。曾经认为 ECM 是不可穿透的。基于质谱的蛋白质组学已被证明是解码 ECM 的有力工具。鉴于过去十年取得的进展,有理由相信基质组的深入探索是可行的,我们可能很快就会见证 ECM 蛋白质组学的第一个转化应用。