首页> 外文期刊>Frontiers in Pharmacology >Copper Chaperone for Superoxide Dismutase Promotes Breast Cancer Cell Proliferation and Migration via ROS-Mediated MAPK/ERK Signaling
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Copper Chaperone for Superoxide Dismutase Promotes Breast Cancer Cell Proliferation and Migration via ROS-Mediated MAPK/ERK Signaling

机译:铜伴侣蛋白用于超氧化物歧化酶通过ROS介导的ROS介导的MAPK / ERK信号促进乳腺癌细胞的增殖和迁移

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Copper chaperone for superoxide dismutase (CCS) is a critical component of oxidation–reduction system and functions as a potential tumor promoter in several cancers. However, the function and clinical significance of CCS in breast cancer remain unclear. Here, we found CCS was highly expressed in breast cancer, where it promoted breast cancer cell proliferation and migration. Suppression of CCS expression was sufficient to attenuate the phosphorylation level of ERK1/2 and increase the accumulation of reactive oxygen species (ROS). Mechanistically, we found that knockdown of CCS decreases the activity of ERK1/2 mediated by the accumulation of ROS, which leads to the inhibition of cell proliferation and migration. In summary, these results indicated that CCS promotes the growth and migration of breast cancer cells via regulating the ERK1/2 activity mediated by ROS.
机译:用于超氧化物歧化酶(CCS)的铜伴侣蛋白是氧化还原系统的重要组成部分,并在几种癌症中起着潜在的肿瘤促进剂的作用。但是,CCS在乳腺癌中的功能和临床意义尚不清楚。在这里,我们发现CCS在乳腺癌中高表达,并促进乳腺癌细胞的增殖和迁移。 CCS表达的抑制足以减弱ERK1 / 2的磷酸化水平并增加活性氧(ROS)的积累。从机制上,我们发现敲低CCS会降低由ROS积累介导的ERK1 / 2的活性,从而抑制细胞的增殖和迁移。总之,这些结果表明,CCS通过调节ROS介导的ERK1 / 2活性来促进乳腺癌细胞的生长和迁移。

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