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信号转导和转录激活因子5A(STAT5A)介导的NADPH氧化酶5样蛋白(NOX5-L)表达促进乳腺癌细胞的增殖和转移。

STAT5A-mediated NOX5-L expression promotes the proliferation and metastasis of breast cancer cells.

作者信息

Dho So Hee, Kim Ji Young, Lee Kwang-Pyo, Kwon Eun-Soo, Lim Jae Cheong, Kim Chang-Jin, Jeong Dongjun, Kwon Ki-Sun

机构信息

Aging Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Republic of Korea; Radioisotope Research Division, Department of Research Reactor Utilization, Korea Atomic Energy Research Institute, Daejeon 305-353, Republic of Korea.

Aging Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Republic of Korea.

出版信息

Exp Cell Res. 2017 Feb 1;351(1):51-58. doi: 10.1016/j.yexcr.2016.12.020. Epub 2016 Dec 26.

Abstract

NADPH oxidase (NOX) generates reactive oxygen species (ROS) and has been suggested to mediate cell proliferation in some cancers. Here, we show that an increase in the expression of NOX5 long form (NOX5-L) is critical for tumor progression in breast tumor tissues. Immunostaining of clinical samples indicated that NOX5 was overexpressed in 41.1% of breast ductal carcinoma samples. NOX5-L depletion consistently suppressed cell proliferation, invasion, and migration in vitro. Antibody-mediated neutralization of NOX5-L attenuated tumor progression in a mouse xenograft model. Promoter analysis revealed that NOX5-L expression is regulated by STAT5A in breast cancer cells. Based on our novel findings, we suggest that inhibition of NOX5-L may be a promising therapeutic strategy that exerts anti-cancer effects via the modulation of ROS-mediated cell signaling.

摘要

NADPH氧化酶(NOX)可产生活性氧(ROS),并且有人提出它在某些癌症中介导细胞增殖。在此,我们表明NOX5长亚型(NOX5-L)表达的增加对乳腺肿瘤组织中的肿瘤进展至关重要。临床样本的免疫染色表明,41.1%的乳腺导管癌样本中NOX5过表达。在体外,NOX5-L缺失持续抑制细胞增殖、侵袭和迁移。抗体介导的NOX5-L中和作用减弱了小鼠异种移植模型中的肿瘤进展。启动子分析显示,在乳腺癌细胞中,NOX5-L的表达受STAT5A调控。基于我们的新发现,我们认为抑制NOX5-L可能是一种有前景的治疗策略,它通过调节ROS介导的细胞信号传导发挥抗癌作用。

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