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花生四烯酸通过PI3K/Akt依赖途径促进MDA-MB-231乳腺癌细胞的迁移和侵袭。

Arachidonic acid promotes migration and invasion through a PI3K/Akt-dependent pathway in MDA-MB-231 breast cancer cells.

作者信息

Villegas-Comonfort Socrates, Castillo-Sanchez Rocio, Serna-Marquez Nathalia, Cortes-Reynosa Pedro, Salazar Eduardo Perez

机构信息

Departamento de Biologia Celular, Cinvestav-IPN, Av. IPN # 2508, San Pedro Zacatenco, Mexico DF 07360, Mexico.

Departamento de Biologia Celular, Cinvestav-IPN, Av. IPN # 2508, San Pedro Zacatenco, Mexico DF 07360, Mexico.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 2014 May;90(5):169-77. doi: 10.1016/j.plefa.2014.01.007. Epub 2014 Feb 12.

Abstract

Arachidonic acid (AA) is a common dietary n-6 cis polyunsaturated fatty acid that under physiological conditions is present in an esterified form in cell membrane phospholipids, however it might be present in the extracellular microenvironment. AA and its metabolites mediate FAK activation, adhesion and migration in MDA-MB-231 breast cancer cells. However, it remains to be investigated whether AA promotes invasion and the signal transduction pathways involved in migration and invasion. Here, we demonstrate that AA induces Akt2 activation and invasion in MDA-MB-231 cells. Akt2 activation requires the activity of Src, EGFR, and PIK3, whereas migration and invasion require Akt, PI3K, EGFR and metalloproteinases activity. Moreover, AA also induces NFκB-DNA binding activity through a PI3K and Akt-dependent pathway. Our findings demonstrate, for the first time, that Akt/PI3K and EGFR pathways mediate migration and invasion induced by AA in MDA-MB-231 breast cancer cells.

摘要

花生四烯酸(AA)是一种常见的膳食n-6顺式多不饱和脂肪酸,在生理条件下以酯化形式存在于细胞膜磷脂中,但也可能存在于细胞外微环境中。AA及其代谢产物介导MDA-MB-231乳腺癌细胞中的粘着斑激酶(FAK)激活、粘附和迁移。然而,AA是否促进侵袭以及参与迁移和侵袭的信号转导途径仍有待研究。在此,我们证明AA诱导MDA-MB-231细胞中Akt2激活和侵袭。Akt2激活需要Src、表皮生长因子受体(EGFR)和磷脂酰肌醇-3激酶(PI3K)的活性,而迁移和侵袭需要Akt、PI3K、EGFR和金属蛋白酶的活性。此外,AA还通过PI3K和Akt依赖性途径诱导核因子κB(NFκB)与DNA的结合活性。我们的研究结果首次证明,Akt/PI3K和EGFR途径介导AA诱导的MDA-MB-231乳腺癌细胞的迁移和侵袭。

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