Fuentes Pedro, Sesé Marta, Guijarro Pedro J, Emperador Marta, Sánchez-Redondo Sara, Peinado Héctor, Hümmer Stefan, Ramón Y Cajal Santiago
Translational Molecular Pathology, Vall d'Hebron Research Institute (VHIR), Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Spanish Biomedical Research Network Centre in Oncology (CIBERONC), Madrid, Spain.
Nat Commun. 2020 Aug 26;11(1):4261. doi: 10.1038/s41467-020-18081-9.
Metastasis, the spread of malignant cells from a primary tumour to distant sites, causes 90% of cancer-related deaths. The integrin ITGB3 has been previously described to play an essential role in breast cancer metastasis, but the precise mechanisms remain undefined. We have now uncovered essential and thus far unknown roles of ITGB3 in vesicle uptake. The functional requirement for ITGB3 derives from its interactions with heparan sulfate proteoglycans (HSPGs) and the process of integrin endocytosis, allowing the capture of extracellular vesicles and their endocytosis-mediated internalization. Key for the function of ITGB3 is the interaction and activation of focal adhesion kinase (FAK), which is required for endocytosis of these vesicles. Thus, ITGB3 has a central role in intracellular communication via extracellular vesicles, proposed to be critical for cancer metastasis.
转移,即恶性细胞从原发性肿瘤扩散到远处部位,导致90%的癌症相关死亡。整合素ITGB3此前已被描述在乳腺癌转移中起关键作用,但其确切机制仍不明确。我们现在发现了ITGB3在囊泡摄取中迄今未知的重要作用。ITGB3的功能需求源于其与硫酸乙酰肝素蛋白聚糖(HSPG)的相互作用以及整合素内吞作用过程,从而实现对细胞外囊泡的捕获及其通过内吞作用介导的内化。ITGB3功能的关键在于粘着斑激酶(FAK)的相互作用和激活,这是这些囊泡内吞所必需的。因此,ITGB3在通过细胞外囊泡进行的细胞内通讯中起核心作用,这被认为对癌症转移至关重要。