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Rho 激酶抑制剂法舒地尔通过下调肺癌细胞系 A549 中 VEGF 的表达抑制迁移和侵袭。

Rho kinase inhibitor fasudil suppresses migration and invasion though down-regulating the expression of VEGF in lung cancer cell line A549.

机构信息

Department of Oncology, The Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 430022, Wuhan, China.

出版信息

Med Oncol. 2011 Jun;28(2):565-71. doi: 10.1007/s12032-010-9468-5. Epub 2010 Mar 19.

Abstract

Rho and Rho-associated kinase play an important role in focal adhesion, stress fiber formation and cell motility. Fasudil is a kind of Rho kinase inhibitor. The effect and precise molecular mechanism of fasudil on the biology behavior of lung cancer cell A549 remains unclear. The cytotoxic effect of fasudil on A549 cell was measured by 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Wound-healing assay was used to evaluate the effect of fasudil on migration activity of A549 cells. The invasion activity of A549 cells was detected by transwell chamber assay. The expression of MMPs was measured by gelatin zymography. RT-PCR and western blot were used to investigate the molecular change of A549 cells after treated with fasudil. Fasudil-inhibited proliferation of A549 cells in a concentration-dependent manner, decreased the migration and invasion activity. After treated with fasudil, the expression of MMP-2 and MMP-9 was significantly inhibited compared with the control group. Furthermore, the expression of RhoA and VEGF of A549 cell treated with fasudil was significantly down-regulated. Our findings indicate that fasudil might have a therapeutic potential for lung cancer though inhibiting cell proliferation, migration, invasion, MMPs activity and down-regulating the expression of RhoA and VEGF.

摘要

Rho 和 Rho 相关激酶在黏附斑、应力纤维形成和细胞迁移中发挥重要作用。法舒地尔是一种 Rho 激酶抑制剂。法舒地尔对肺癌细胞 A549 生物学行为的影响及其确切的分子机制尚不清楚。通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法测量法舒地尔对 A549 细胞的细胞毒性作用。划痕愈合试验用于评估法舒地尔对 A549 细胞迁移活性的影响。Transwell 室试验检测 A549 细胞的侵袭活性。明胶酶谱法测量 MMPs 的表达。RT-PCR 和 Western blot 用于研究法舒地尔处理后 A549 细胞的分子变化。法舒地尔呈浓度依赖性抑制 A549 细胞的增殖,降低迁移和侵袭活性。与对照组相比,法舒地尔处理后 MMP-2 和 MMP-9 的表达明显受到抑制。此外,法舒地尔处理的 A549 细胞中 RhoA 和 VEGF 的表达明显下调。我们的研究结果表明,法舒地尔可能通过抑制细胞增殖、迁移、侵袭、MMPs 活性以及下调 RhoA 和 VEGF 的表达,对肺癌具有治疗潜力。

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