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Nuclear NADPH oxidase-4 associated with disease progression in renal cell carcinoma.
Kaushik, Dharam; Ashcraft, Keith A; Wang, Hanzhang; Shanmugasundaram, Karthigayan; Shah, Pankil K; Gonzalez, Gabriela; Nazarullah, Alia; Tye, Cooper B; Liss, Michael A; Pruthi, Deepak K; Mansour, Ahmed M; Chowdhury, Wasim; Bacich, Dean; Zhang, Hao; Watson, Amanda L; Block, Karen; O'Keefe, Denise; Rodriguez, Ronald.
Afiliação
  • Kaushik D; Department of Urology, University of Texas Health, San Antonio, Texas. Electronic address: kaushik@uthscsa.edu.
  • Ashcraft KA; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Wang H; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Shanmugasundaram K; Department of Molecular Medicine, University of Texas Health, San Antonio, Texas.
  • Shah PK; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Gonzalez G; Department of Pathology, University of Texas Health, San Antonio, Texas.
  • Nazarullah A; Department of Pathology, University of Texas Health, San Antonio, Texas.
  • Tye CB; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Liss MA; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Pruthi DK; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Mansour AM; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Chowdhury W; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Bacich D; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Zhang H; Department of Cellular and Molecular Medicine, University of Arizona, Phoenix, Arizona.
  • Watson AL; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Block K; Office of Research and Development, Veteran Affairs, Washington, District of Columbia.
  • O'Keefe D; Department of Urology, University of Texas Health, San Antonio, Texas.
  • Rodriguez R; Department of Urology, University of Texas Health, San Antonio, Texas.
Transl Res ; 223: 1-14, 2020 09.
Article em En | MEDLINE | ID: mdl-32492552
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Núcleo Celular / Progressão da Doença / NADPH Oxidase 4 / Neoplasias Renais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Núcleo Celular / Progressão da Doença / NADPH Oxidase 4 / Neoplasias Renais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article