焦点粘着
基质金属蛋白酶
细胞外基质
癌细胞
PI3K/AKT/mTOR通路
细胞生物学
细胞粘附
整合素
入侵足纲
化学
癌症
蛋白激酶B
癌症研究
细胞迁移
磷酸化
信号转导
生物
细胞
生物化学
遗传学
作者
Raffaele Carrano,Martina Grande,Eleonora Leti Maggio,Carlotta Zucca,Riccardo Bei,Riccardo Bei,Camilla Palumbo,Chiara Focaccetti,Daniela Nardozi,Valeria Lucarini,Valentina Angiolini,Patrizia Mancini,Francesca Barberini,Giovanni Barillari,Loredana Cifaldi,Laura Masuelli,Monica Benvenuto,Roberto Bei,Roberto Bei
出处
期刊:Biomedicines
[Multidisciplinary Digital Publishing Institute]
日期:2024-02-21
卷期号:12 (3): 482-482
被引量:11
标识
DOI:10.3390/biomedicines12030482
摘要
Focal adhesion plaques (FAPs) play an important role in the communication between cells and the extracellular matrix (ECM) and in cells' migration. FAPs are macromolecular complexes made by different proteins which also interact with matrix metalloproteinases (MMPs). Because of these fundamental properties, FAPs and MMPs are also involved in cancer cells' invasion and in the metastatic cascade. The most important proteins involved in FAP formation and activity are (i) integrins, (ii) a complex of intracellular proteins and (iii) cytoskeleton proteins. The latter, together with MMPs, are involved in the formation of filopodia and invadopodia needed for cell movement and ECM degradation. Due to their key role in cancer cell migration and invasion, MMPs and components of FAPs are often upregulated in cancer and are thus potential targets for cancer therapy. Polyphenols, a large group of organic compounds found in plant-based food and beverages, are reported to have many beneficial healthy effects, including anticancer and anti-inflammatory effects. In this review, we discuss the growing evidence which demonstrates that polyphenols can interact with the different components of FAPs and MMPs, inhibit various pathways like PI3K/Akt, lower focal adhesion kinase (FAK) phosphorylation and decrease cancer cells' invasiveness, leading to an overall antitumoral effect. Finally, here we highlight that polyphenols could hold potential as adjunctive therapies to conventional cancer treatments due to their ability to target key mechanisms involved in cancer progression.
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