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NecroX-5可通过降低Rho家族GTP酶的表达来抑制黑色素瘤转移。

NecroX-5 Can Suppress Melanoma Metastasis by Reducing the Expression of Rho-Family GTPases.

作者信息

Moon Gue-Tae, Lee Ji-Hyun, Jeong Sang-Hyun, Jin Song-Wan, Park Young-Min

机构信息

Department of Biomedicine & Health Sciences, The Catholic University of Korea, #222 Banpo-daero, Seocho-gu, Seoul 06591, Korea.

Department of Dermatology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, #222 Banpo-daero, Seocho-gu, Seoul 06591, Korea.

出版信息

J Clin Med. 2021 Jun 25;10(13):2790. doi: 10.3390/jcm10132790.

Abstract

NecroX-5 (NX-5) is a cell-permeable necrosis inhibitor with cytoprotective effects. Although it has been reported to inhibit lung and breast cancer metastasis by modulating migration, its therapeutic effect on melanoma metastasis is still unknown. In this study, we examined the anti-metastatic effect of NX-5 on melanoma cell lines and its related therapeutic mechanism. The anti-metastatic effect of NX-5 on melanoma cell lines was determined using a transwell migration assay. We performed a quantitative real-time polymerase chain reaction and western blot analysis to measure changes in the expression of mRNA and protein, respectively, for major mediators of Rho-family GTPases after NX-5 treatment in melanoma cells. In addition, after constructing the 3D melanoma model, the expression of Rho-family GTPases was measured by immunohistochemistry. NX-5 (10 μM and 20 μM) treatment significantly reduced melanoma cell migration ( < 0.01). Additionally, NX-5 (20 μM) treatment significantly decreased the mRNA and protein expression levels of Cdc42, Rac1, and RhoA in melanoma cells compared with the untreated group ( < 0.001 and < 0.05, respectively). Immunohistochemistry for our 3D melanoma model showed that Cdc42, Rac1, and RhoA were constitutively expressed in the nuclei of melanoma cells of the untreated group, and NX-5 treatment decreased their expression. These results demonstrate that NX-5 can suppress melanoma metastasis by reducing the expression of Rho-family GTPases.

摘要

NecroX-5(NX-5)是一种具有细胞保护作用的可穿透细胞的坏死抑制剂。尽管已有报道称其可通过调节迁移来抑制肺癌和乳腺癌转移,但其对黑色素瘤转移的治疗效果仍不清楚。在本研究中,我们检测了NX-5对黑色素瘤细胞系的抗转移作用及其相关治疗机制。使用Transwell迁移实验测定NX-5对黑色素瘤细胞系的抗转移作用。我们进行了定量实时聚合酶链反应和蛋白质印迹分析,分别测量黑色素瘤细胞经NX-5处理后Rho家族GTP酶主要介质的mRNA和蛋白质表达变化。此外,构建三维黑色素瘤模型后,通过免疫组织化学检测Rho家族GTP酶的表达。NX-5(10μM和20μM)处理显著降低了黑色素瘤细胞的迁移(<0.01)。此外,与未处理组相比,NX-5(20μM)处理显著降低了黑色素瘤细胞中Cdc42、Rac1和RhoA的mRNA和蛋白质表达水平(分别为<0.001和<0.05)。我们的三维黑色素瘤模型免疫组织化学显示,未处理组黑色素瘤细胞核中Cdc42、Rac1和RhoA呈组成性表达,而NX-5处理降低了它们的表达。这些结果表明,NX-5可通过降低Rho家族GTP酶的表达来抑制黑色素瘤转移。

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