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MicroRNA miR-125a-3p modulates molecular pathway of motility and migration in prostate cancer cells

机译:MicroRNA miR-125a-3p调节前列腺癌细胞运动和迁移的分子途径

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摘要

Fyn kinase is implicated in prostate cancer. We illustrate the role of miR-125a-3p in cellular pathways accounted for motility and migration of prostate cancer cells, probably through its regulation on Fyn expression and Fyn-downstream proteins. Prostate cancer PC3 cells were transiently transfected with empty miR-Vec (control) or with miR-125a-3p. Overexpression of miR-125a-3p reduced migration of PC3 cells and increased apoptosis. Live cell confocal imaging indicated that overexpression of miR-125a-3p reduced the cells' track speed and length and impaired phenotype. Fyn, FAK and paxillin, displayed reduced activity following miR-125a-3p overexpression. Accordingly, actin rearrangement and cells' protrusion formation were impaired. An inverse correlation between miR-125a-3p and Gleason score was observed in human prostate cancer tissues. Our study demonstrated that miR-125a-3p may regulate migration of prostate cancer cells.
机译:Fyn激酶与前列腺癌有关。我们举例说明了miR-125a-3p在细胞途径中的作用,可能是通过其对Fyn表达和Fyn下游蛋白的调控来解释前列腺癌细胞的运动性和迁移。用空的miR-Vec(对照)或miR-125a-3p瞬时转染前列腺癌PC3细胞。 miR-125a-3p的过表达减少PC3细胞的迁移并增加凋亡。活细胞共聚焦成像表明,miR-125a-3p的过表达降低了细胞的追踪速度和长度,并损害了表型。 Fyn,FAK和paxillin在miR-125a-3p过表达后显示活性降低。因此,肌动蛋白重排和细胞突起形成受损。在人类前列腺癌组织中观察到miR-125a-3p与Gleason评分呈负相关。我们的研究表明,miR-125a-3p可能调节前列腺癌细胞的迁移。

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