Literature DB >> 23851018

Characterization of NADPH oxidase 5 expression in human tumors and tumor cell lines with a novel mouse monoclonal antibody.

Smitha Antony1, Yongzhong Wu1, Stephen M Hewitt2, Miriam R Anver3, Donna Butcher3, Guojian Jiang1, Jennifer L Meitzler1, Han Liu4, Agnes Juhasz1, Jiamo Lu1, Krishnendu K Roy4, James H Doroshow5.   

Abstract

Reactive oxygen species generated by NADPH oxidase 5 (Nox5) have been implicated in physiological and pathophysiological signaling pathways, including cancer development and progression. However, because immunological tools are lacking, knowledge of the role of Nox5 in tumor biology has been limited; the expression of Nox5 protein across tumors and normal tissues is essentially unknown. Here, we report the characterization and use of a mouse monoclonal antibody against a recombinant Nox5 protein (bp 600-746) for expression profiling of Nox5 in human tumors by tissue microarray analysis. Using our novel antibody, we also report the detection of endogenous Nox5 protein in human UACC-257 melanoma cells. Immunofluorescence, confocal microscopy, and immunohistochemical techniques were employed to demonstrate Nox5 localization throughout UACC-257 cells, with perinuclear enhancement. Tissue microarray analysis revealed, for the first time, substantial Nox5 overexpression in several human cancers, including those of prostate, breast, colon, lung, brain, and ovary, as well as in malignant melanoma and non-Hodgkin lymphoma; expression in most nonmalignant tissues was negative to weak. This validated mouse monoclonal antibody will promote further exploration of the functional significance of Nox5 in human pathophysiology, including tumor cell growth and proliferation.
Copyright © 2013. Published by Elsevier Inc.

Entities:  

Keywords:  Duox; Free radicals; Melanoma; Mouse monoclonal Nox5 antibody; NADPH oxidase; NADPH oxidase 5; Nox; ROS; Reactive oxygen species; Superoxide; Tissue microarray; UACC-257 cells; dual oxidase; reactive oxygen species

Mesh:

Substances:

Year:  2013        PMID: 23851018      PMCID: PMC3859815          DOI: 10.1016/j.freeradbiomed.2013.07.005

Source DB:  PubMed          Journal:  Free Radic Biol Med        ISSN: 0891-5849            Impact factor:   7.376


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