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Downregulation of aquaporin 3 inhibits cellular proliferation migration and invasion in the MDA-MB-231 breast cancer cell line

机译:水通道蛋白3的下调抑制了MDA-MB-231乳腺癌细胞系中的细胞增殖迁移和侵袭

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摘要

Aquaporins are membrane proteins that regulate cellular water flow. Recently, aquaporins have been proposed as mediators of cancer cell biology. A subset of aquaporins, referred to as aquaglyceroporins are known to facilitate the transport of glycerol. The present study describes the effect of gene knockdown of the aquaglyceroporin AQP3 on MDA-MB-231 breast cancer cell proliferation, migration, invasion, adherence and response to the chemotherapeutic agent 5-fluorouracil. shRNA mediated AQP3 gene knockdown induced a 28% reduction in cellular proliferation (P<0.01), a 39% decrease in migration (P<0.0001), a 24% reduction in invasion (P<0.05) and a 25% increase in cell death at 100 µM 5-FU (P<0.01). Analysis of cell permeability to water and glycerol revealed that MDA-MB-231 cells with knocked down AQP3 demonstrated a modest decrease in water permeability (17%; P<0.05) but a more marked decrease in glycerol permeability (77%; P<0.001). These results suggest that AQP3 has a role in multiple aspects of breast cancer cell pathophysiology and therefore represents a novel target for therapeutic intervention.
机译:水通道蛋白是调节细胞水流量的膜蛋白。最近,已经提出水通道蛋白作为癌细胞生物学的介质。已知水通道蛋白的子集称为水甘油通道蛋白,其促进甘油的运输。本研究介绍了基因的水甘油糖蛋白AQP3基因敲低对MDA-MB-231乳腺癌细胞增殖,迁移,侵袭,粘附和对化学治疗剂5-氟尿嘧啶的反应的影响。 shRNA介导的AQP3基因敲低诱导细胞增殖减少28%(P <0.01),迁移减少39%(P <0.0001),侵袭减少24%(P <0.05),细胞死亡增加25% 100 µM 5-FU(P <0.01)。细胞对水和甘油的渗透性分析表明,敲低AQP3的MDA-MB-231细胞显示出适度的水渗透性降低(17%; P <0.05),但甘油的渗透性降低更为明显(77%; P <0.001) )。这些结果表明,AQP3在乳腺癌细胞病理生理学的多个方面具有作用,因此代表了治疗干预的新靶标。

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