| Literature DB >> 28034671 |
So Hee Dho1, Ji Young Kim2, Kwang-Pyo Lee2, Eun-Soo Kwon2, Jae Cheong Lim3, Chang-Jin Kim4, Dongjun Jeong5, Ki-Sun Kwon6.
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.Entities:
Keywords: Cancer/ NOX5-L/ ROS/ STAT5A
Mesh:
Substances:
Year: 2016 PMID: 28034671 DOI: 10.1016/j.yexcr.2016.12.020
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905