Institut National de la Recherche Scientifique (INRS), EMT Research Center, 1650 boul. Lionel-Boulet, Varennes, J3X 1S2, Canada.
Leslie Dan Faculty of Pharmacy, University of Toronto, 144 College Street, Toronto, Ontario M5S 3M2, Canada.
Theranostics. 2020 Jan 12;10(4):1960-1980. doi: 10.7150/thno.39995. eCollection 2020.
It is currently challenging to eradicate cancer. In the case of solid tumors, the dense and aberrant extracellular matrix (ECM) is a major contributor to the heterogeneous distribution of small molecule drugs and nano-formulations, which makes certain areas of the tumor difficult to treat. As such, much research is devoted to characterizing this matrix and devising strategies to modify its properties as a means to facilitate the improved penetration of drugs and their nano-formulations. This contribution presents the current state of knowledge on the composition of normal ECM and changes to ECM that occur during the pathological progression of cancer. It also includes discussion of strategies designed to modify the composition/properties of the ECM as a means to enhance the penetration and transport of drugs and nano-formulations within solid tumors. Moreover, a discussion of approaches to image the ECM, as well as ways to monitor changes in the ECM as a function of time are presented, as these are important for the implementation of ECM-modifying strategies within therapeutic interventions. Overall, considering the complexity of the ECM, its variability within different tissues, and the multiple pathways by which homeostasis is maintained (both in normal and malignant tissues), the available literature - while promising - suggests that improved monitoring of ECM remodeling is needed to harness the described strategies to their full potential, and match them with an appropriate chemotherapy regimen.
目前,癌症的根治仍具挑战性。在实体肿瘤的情况下,致密且异常的细胞外基质(ECM)是导致小分子药物和纳米制剂不均匀分布的主要因素,这使得肿瘤的某些区域难以治疗。因此,大量研究致力于对该基质进行特征描述,并设计策略来改变其性质,以促进药物及其纳米制剂的更好渗透。本研究介绍了正常 ECM 的组成以及癌症病理进展过程中 ECM 发生的变化的最新知识。还讨论了旨在改变 ECM 组成/性质的策略,以增强药物和纳米制剂在实体瘤内的渗透和转运。此外,还讨论了成像 ECM 的方法,以及作为监测 ECM 随时间变化的功能,因为这些对于在治疗干预中实施 ECM 修饰策略非常重要。总的来说,考虑到 ECM 的复杂性、不同组织中 ECM 的可变性以及维持内稳态的多种途径(在正常组织和恶性组织中均如此),尽管现有文献很有前景,但仍需要更好地监测 ECM 的重塑,以充分发挥所述策略的潜力,并将其与适当的化疗方案相匹配。