Literature DB >> 32492552

Nuclear NADPH oxidase-4 associated with disease progression in renal cell carcinoma.

Dharam Kaushik1, Keith A Ashcraft2, Hanzhang Wang2, Karthigayan Shanmugasundaram3, Pankil K Shah2, Gabriela Gonzalez4, Alia Nazarullah4, Cooper B Tye2, Michael A Liss2, Deepak K Pruthi2, Ahmed M Mansour2, Wasim Chowdhury2, Dean Bacich2, Hao Zhang5, Amanda L Watson2, Karen Block6, Denise O'Keefe2, Ronald Rodriguez2.   

Abstract

Nuclear NADPH oxidase-4 (Nox4) is a key component of metabolic reprogramming and is often overexpressed in renal cell carcinoma (RCC). However, its prognostic role in RCC remains unclear. Here we examined the significance of nuclear Nox4 on disease progression and development of drug resistance in advanced RCC. We analyzed human RCC tissue from multiple regions in the primary index tumor, cancer-associated normal adjacent parenchyma, intravascular tumor in locally advanced cancer patients. We found that the higher nuclear Nox4 expression was significantly associated with progression and death. These findings were consistent after controlling for other competing clinical variables. In contrast, patients with lower nuclear Nox4, even in higher stage RCC had better prognosis. We identified a subset of patients with high nuclear Nox4 who had rapid disease progression or died within 6 months of surgery. In addition, higher nuclear Nox4 level correlated with resistance to targeted therapy and immunotherapy. Western blotting performed on fresh human RCC tissue as well as cell-lines revealed increased nuclear Nox4 expression. Our data support an important prognostic role of Nox4 mediated regulation of RCC independent of other competing variables. Nox4 localizes to the nucleus in high-grade, high-stage RCC. Higher nuclear Nox4 has prognostic significance for disease progression, poor survival, and development of drug resistance in RCC.
Copyright © 2020 Elsevier Inc. All rights reserved.

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Year:  2020        PMID: 32492552      PMCID: PMC8111697          DOI: 10.1016/j.trsl.2020.05.009

Source DB:  PubMed          Journal:  Transl Res        ISSN: 1878-1810            Impact factor:   7.012


  29 in total

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Authors:  Hiromi I Wettersten; Omran Abu Aboud; Primo N Lara; Robert H Weiss
Journal:  Nat Rev Nephrol       Date:  2017-05-08       Impact factor: 28.314

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5.  Long-term results of resection of renal cell cancer with extension into inferior vena cava.

Authors:  J A Libertino; L Zinman; E Watkins
Journal:  J Urol       Date:  1987-01       Impact factor: 7.450

6.  Subcellular localization of Nox4 and regulation in diabetes.

Authors:  Karen Block; Yves Gorin; Hanna E Abboud
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-17       Impact factor: 11.205

7.  Production of tissue microarrays, immunohistochemistry staining and digitalization within the human protein atlas.

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Journal:  J Vis Exp       Date:  2012-05-31       Impact factor: 1.355

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9.  Isotope Tracing of Human Clear Cell Renal Cell Carcinomas Demonstrates Suppressed Glucose Oxidation In Vivo.

Authors:  Kevin D Courtney; Divya Bezwada; Tomoyuki Mashimo; Kumar Pichumani; Vamsidhara Vemireddy; Alexander M Funk; Jennifer Wimberly; Sarah S McNeil; Payal Kapur; Yair Lotan; Vitaly Margulis; Jeffrey A Cadeddu; Ivan Pedrosa; Ralph J DeBerardinis; Craig R Malloy; Robert M Bachoo; Elizabeth A Maher
Journal:  Cell Metab       Date:  2018-08-23       Impact factor: 27.287

10.  NADPH oxidase NOX4 is a glycolytic regulator through mROS-HIF1α axis in thyroid carcinomas.

Authors:  Ping Tang; Hao Dang; Jie Huang; Tao Xu; Ping Yuan; Jun Hu; Jian-Feng Sheng
Journal:  Sci Rep       Date:  2018-10-26       Impact factor: 4.379

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3.  ARID1A knockdown enhances carcinogenesis features and aggressiveness of Caco-2 colon cancer cells: An in vitro cellular mechanism study.

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