首页> 外文期刊>Molecular cancer research: MCR >Intrathecal administration of y-27632, a specific rho-associated kinase inhibitor, for rat neoplastic meningitis.
【24h】

Intrathecal administration of y-27632, a specific rho-associated kinase inhibitor, for rat neoplastic meningitis.

机译:鞘内注射y-27632,一种特定的rho相关激酶抑制剂,用于大鼠肿瘤性脑膜炎。

获取原文
获取原文并翻译 | 示例
           

摘要

The small GTP-binding protein Rho and its target Rho-associated kinase trigger an intracellular signaling cascade that controls actin cytoskeleton and plays an essential role in cell motility and adhesion. A specific Rho-associated kinase inhibitor, Y-27632, has been reported to inhibit cancer invasion. Clinically, disseminated tumor cells in the cerebrospinal fluid invade the intraparenchymal region, damaging the brain and nerves, resulting in fatal brain stem dysfunction, despite intrathecal chemotherapy. To expand therapeutic options for this devastating neoplastic meningitis, we evaluated the potential use of intrathecal Y-27632 administration by employing Walker 256 cells, a rat mammary cancer cell line. Y-27632 dose-dependently inhibited chemotactic and invasive activity of Walker 256 cells. Y-27632 also inhibited the phosphorylation level of regulatory myosin light chain in vitro, but the effect was temporary and was considerably diminished within 16 hours. Y-27632 induced striking morphologic changes in Walker 256 cells, as evidenced by decreased cell-matrix adhesion in culture dishes and three-dimensional collagen I gels, and slightly inhibited colony formation in soft agar. Nevertheless, this drug treatment did not affect Walker 256 cell growth rate. We were able to administer continuous delivery of this inhibitor using an osmotic pump and maintaining drug concentration of 10 mumol/L within the brain. Importantly, this concentration of Y-27632 showed minimal neurotoxicity both in vitro and in vivo. We found that an intrathecal therapy, combining 5-fluoro-2'-deoxyuridine with Y-27632, significantly increased the survival time of rats bearing meningeal carcinomatosis in comparison with animals treated with 5-fluoro-2'-deoxyuridine alone. Taken together, our findings indicate that continuous intrathecal administration of Y-27632 could be a promising therapeutic method when combined with chemotherapy for treating human neoplastic meningitis.
机译:小GTP结合蛋白Rho及其靶标Rho相关激酶触发细胞内信号传导级联反应,该信号传导级联控制肌动蛋白细胞骨架,并在细胞运动和粘附中起重要作用。据报道,一种特定的Rho相关激酶抑制剂Y-27632可抑制癌症的侵袭。临床上,尽管进行鞘内化疗,但脑脊液中已扩散的肿瘤细胞侵入实质内区域,损害了大脑和神经,导致致命的脑干功能障碍。为了扩大针对这种破坏性肿瘤性脑膜炎的治疗选择,我们通过采用大鼠乳腺癌细胞系Walker 256细胞评估了鞘内注射Y-27632的潜在用途。 Y-27632剂量依赖性地抑制Walker 256细胞的趋化和侵袭活性。 Y-27632还可以在体外抑制调节性肌球蛋白轻链的磷酸化水平,但这种作用是暂时的,并且在16小时内大大降低。 Y-27632诱导Walker 256细胞发生了惊人的形态变化,这在培养皿和三维I型胶原凝胶中细胞基质的粘附性降低中得到了证明,并在软琼脂中略微抑制了菌落的形成。尽管如此,这种药物治疗并未影响Walker 256细胞的生长速度。我们能够使用渗透泵连续递送这种抑制剂,并使脑内药物浓度保持在10μmol/ L。重要的是,此浓度的Y-27632在体外和体内均显示出最小的神经毒性。我们发现,与仅接受5-氟-2'-脱氧尿苷治疗的动物相比,将5-氟-2'-脱氧尿苷与Y-27632结合进行鞘内治疗显着增加了患有脑膜癌的大鼠的存活时间。综上所述,我们的发现表明,与化学疗法联合治疗人肿瘤性脑膜炎时,连续鞘内施用Y-27632可能是一种有前途的治疗方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号