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Interaction of brain fatty acid-binding protein with the polyunsaturated fatty acid environment as a potential determinant of poor prognosis in malignant glioma

机译:脑脂肪酸结合蛋白与多不饱和脂肪酸环境的相互作用可能是恶性神经胶质瘤预后不良的潜在决定因素

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摘要

Malignant gliomas are the most common adult brain cancers. In spite of aggressive treatment, recurrence occurs in the great majority of patients and is invariably fatal. Polyunsaturated fatty acids are abundant in brain, particularly ω-6 arachidonic acid (AA) and ω-3 docosahexaenoic acid (DHA). Although the levels of ω-6 and ω-3 polyunsaturated fatty acids are tightly regulated in brain, the ω-6:ω-3 ratio is dramatically increased in malignant glioma, suggesting deregulation of fundamental lipid homeostasis in brain tumor tissue. The migratory properties of malignant glioma cells can be modified by altering the ratio of AA:DHA in growth medium, with increased migration observed in AA-rich medium. This fatty acid-dependent effect on cell migration is dependent on expression of the brain fatty acid binding protein (FABP7) previously shown to bind DHA and AA. Increased levels of enzymes involved in eicosanoid production in FABP7-positive malignant glioma cells suggest that FABP7 is an important modulator of AA metabolism. We provide evidence that increased production of eicosanoids in FABP7-positive malignant glioma growing in an AA-rich environment contributes to tumor infiltration in the brain. We discuss pathways and molecules that may underlie FABP7/AA-mediated promotion of cell migration and FABP7/DHA-mediated inhibition of cell migration in malignant glioma.
机译:恶性神经胶质瘤是最常见的成人脑癌。尽管采取了积极的治疗措施,但绝大多数患者仍会复发,并且总是致命的。脑中富含多不饱和脂肪酸,尤其是ω-6花生四烯酸(AA)和ω-3二十二碳六烯酸(DHA)。尽管脑中ω-6和ω-3多不饱和脂肪酸的含量受到严格调节,但恶性神经胶质瘤中ω-6:ω-3的比例却显着增加,表明脑肿瘤组织中基本脂质稳态的失调。恶性神经胶质瘤细胞的迁移特性可以通过改变生长培养基中AA:DHA的比例来改变,而在富含AA的培养基中可以观察到迁移增加。这种对细胞迁移的脂肪酸依赖性作用取决于先前证明与DHA和AA结合的脑脂肪酸结合蛋白(FABP7)的表达。 FABP7阳性恶性神经胶质瘤细胞中参与类花生酸生产的酶水平增加表明,FABP7是AA代谢的重要调节剂。我们提供的证据表明,在富含AA的环境中生长的FABP7阳性恶性神经胶质瘤中类花生酸的产生增加,有助于大脑中的肿瘤浸润。我们讨论了可能是FABP7 / AA介导的细胞迁移促进和FABP7 / DHA介导的恶性神经胶质瘤细胞迁移抑制的基础的途径和分子。

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