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羽扇豆醇通过抑制 RhoA-ROCK1 信号通路抑制结直肠癌细胞的迁移和侵袭。

Lupeol inhibits migration and invasion of colorectal cancer cells by suppressing RhoA-ROCK1 signaling pathway.

机构信息

School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, 325000, China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2020 Nov;393(11):2185-2196. doi: 10.1007/s00210-020-01815-3. Epub 2020 Feb 6.

Abstract

Metastasis is the main cause of death in colorectal cancer (CRC) patients. However, current treatment options for CRC metastasis are very limited. Lupeol, a triterpene that is widely found in vegetables and fruits, has been reported to possess the cancer-preventive and anti-inflammatory functions. However, the roles of Lupeol in the migration and invasion of colorectal cancer remain unclear. Here, we evaluated the effect of Lupeol treatment on colorectal cancer cell lines, HCT116 and SW620, and delineated its underlying mechanisms. Our results showed that Lupeol induced a dose-dependent inhibition of HCT116 and SW620 cells viability, measured by CCK8 assay. Wound healing and Transwell migration and invasion assays revealed that Lupeol significantly suppressed the migration and invasion of CRC cells. Using laser confocal microscope, we observed that the pseudopods and protrusions of HCT116 and SW620 cells decreased and disrupted after treatment with Lupeol. In addition, the quantitative real-time PCR and Western blotting results showed that Lupeol downregulated the expression of RhoA and RhoC, and their downstream effectors ROCK1, Cofilin, p-MLC, and the associated regulatory protein Cyclin A2. Interestingly, the migration and invasion capacity of CRC cells was reduced after RhoA knockdown. And there were no additional changes in CRC cells with RhoA knockdown to treat with Lupeol. These findings demonstrate that Lupeol can suppress the migration and invasion of colorectal cancer cells by remodeling the actin cytoskeleton via RhoA-ROCK1 pathway inhibition, which may provide an effective anti-metastatic agent for CRC patients.

摘要

转移是结直肠癌(CRC)患者死亡的主要原因。然而,目前 CRC 转移的治疗选择非常有限。羽扇醇,一种广泛存在于蔬菜和水果中的三萜,据报道具有预防癌症和抗炎作用。然而,羽扇醇在结直肠癌迁移和侵袭中的作用尚不清楚。在这里,我们评估了羽扇醇处理对结直肠癌细胞系 HCT116 和 SW620 的影响,并阐明了其潜在机制。我们的结果表明,羽扇醇诱导 HCT116 和 SW620 细胞活力的剂量依赖性抑制,通过 CCK8 测定法测量。划痕愈合和 Transwell 迁移和侵袭实验表明,羽扇醇显著抑制 CRC 细胞的迁移和侵袭。使用激光共聚焦显微镜,我们观察到 HCT116 和 SW620 细胞的伪足和突起在羽扇醇处理后减少并破坏。此外,实时定量 PCR 和 Western blot 结果表明,羽扇醇下调 RhoA 和 RhoC 的表达及其下游效应子 ROCK1、Cofilin、p-MLC 和相关调节蛋白 Cyclin A2。有趣的是,CRC 细胞的迁移和侵袭能力在 RhoA 敲低后降低。并且在 RhoA 敲低的 CRC 细胞中用 Lupeol 处理后没有发生其他变化。这些发现表明,Lupeol 通过抑制 RhoA-ROCK1 通路抑制肌动蛋白细胞骨架重塑,从而抑制结直肠癌细胞的迁移和侵袭,可能为 CRC 患者提供有效的抗转移药物。

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