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Progranulin Stimulated by LPA Promotes the Migration of Aggressive Breast Cancer Cells

机译:LPA刺激的前颗粒蛋白可促进侵袭性乳腺癌细胞的迁移。

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Activator and inhibitor roles for the 88-kDa-secreted glycoprotein progranulin (PGRN) have been demonstrated in ovarian cancer cells. Here, we investigated the effects of PGRN in breast cancer migration. Testing MCF7, MDA-MB-453, and MDA-MB-231 human breast cancer cells and the MCF10A breast epithelial cell line, we demonstrate that LPA-induced PGRN stimulation led to a significant increase in cell invasion of MDA-MB-453 and MDA-MB-231 cells only (p 0.05). Moreover, incubation with an anti-PGRN antibody, an inhibitor of the ERK pathway (PD98059) or both in combination inhibited the ability of MDA-MB-231 cells to invade. Furthermore, the expression of focal adhesion kinases promoted by LPA-induced PGRN was also inhibited by PD98059 alone or in combination with an anti-PGRN antibody (p 0.05). Taken together, these results suggest that the LPA activation of PGRN involving the ERK pathway is critical to promote MDA-MB-231 breast cancer cell invasion.
机译:已经在卵巢癌细胞中证明了88 kDa分泌的糖蛋白前颗粒蛋白(PGRN)的激活剂和抑制剂作用。在这里,我们调查了PGRN在乳腺癌迁移中的作用。测试MCF7,MDA-MB-453和MDA-MB-231人乳腺癌细胞以及MCF10A乳腺癌上皮细胞系,我们证明LPA诱导的PGRN刺激导致MDA-MB-453和MDA-MB-453细胞侵袭的显着增加仅MDA-MB-231细胞(p <0.05)。此外,与抗PGRN抗体,ERK途径抑制剂(PD98059)或两者共同孵育可抑制MDA-MB-231细胞侵袭的能力。此外,单独地或与抗PGRN抗体组合的PD98059也抑制了LPA诱导的PGRN促进的粘着斑激酶的表达(p <0.05)。两者合计,这些结果表明涉及ERK途径的PGRN的LPA激活对于促进MDA-MB-231乳腺癌细胞侵袭至关重要。

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