Microglial lysophosphatidic acid promotes glioblastoma proliferation and migration via LPA1 receptor

다국어 초록 (Multilingual Abstract)

Glioblastomas (GBMs) are highly aggressive primary brain tumors characterized by cellular heterogeneity, insensitivity to chemotherapy and poor patient survival. Lysophosphatidic acid (LPA) is a lysophospholipid that acts as a bioactive signaling molecule and plays important roles in diverse biological events during development and disease, including several cancer types. Microglial cells, the resident macrophages of the central nervous system, express high levels of Autotaxin (ATX,Enpp2), an enzyme that synthetizes LPA. Our study aimed to investigate the role of LPA on tumor growth and invasion in the context of microglia‐GBM interaction. First, through bioinformatics studies, patient data analysis demonstrated that more aggressive GBM expressed higher levels of ENPP2, which was also associated with worse patient prognosis with proneural GBM. Using GBM‐microglia co‐culture system we then demonstrated that GBM secreted factors were able to increase LPA1 and ATX in microglia, which could be further enhanced by hypoxia. On the other hand, interaction with microglial cells also increased ATX expression in GBM. Furthermore, microglial‐induced GBM proliferation and migration could be inhibited by pharmacological inhibition of LPA1, suggesting that microglial‐derived LPA could support tumor growth and invasion. Finally, increased LPA1 expression was observed in GBM comparing with other gliomas and could be also associated with worse patient survival. These results show for the first time a microglia‐GBM interaction through the LPA pathway with relevant implications for tumor progression. A better understanding of this interaction can lead to the development of new therapeutic strategies setting LPA as a potential target for GBM treatment.










LPA1 and ATX expression are correlated with glioma aggressiveness and prognosis in patients. Both glioblastoma (GBM) and microglia are capable of secreting LPA in vitro. In this context, GBM induces an increase in LPA1 and ATX expression in microglia. Microglia, in turn, increases ATX expression in GBM cells and induces GBM migration, survival and proliferation via LPA1. These results show for the first time a microglia‐GBM interaction through LPA pathway with relevant implications for tumor progression. A better understanding of this interaction can lead to the development of new therapeutic strategies setting LPA as a potential target for GBM treatment.