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Updated: Jun 20, 2026

Production and Detection of Reactive Oxygen Species (ROS) in Cancers
Published on: November 21, 2011
Intracellular expression of reactive oxygen species-generating NADPH oxidase NOX4 in normal and cancer thyroid
Urbain Weyemi1, Bernard Caillou, Monique Talbot
1CNRS, FRE2939, Villejuif F-94805, France.
Abstract:
NADPH oxidase 4 (NOX4) belongs to the NOX family that generates reactive oxygen species (ROS). Function and tissue distribution of NOX4 have not yet been entirely clarified. To date, in the thyroid gland, only DUOX1/2 NOX systems have been described. NOX4 mRNA expression, as shown by real-time PCR, was present in normal thyroid tissue, regulated by TSH and significantly increased in differentiated cancer tissues. TSH increased the protein level of NOX4 in human thyroid primary culture and NOX4-dependent ROS generation. NOX4 immunostaining was detected in normal and pathologic thyroid tissues. In normal thyroid tissue, staining was heterogeneous and mostly found in activated columnar thyrocytes but absent in quiescent flat cells. Papillary and follicular thyroid carcinomas displayed more homogeneous staining. The p22(phox) protein that forms a heterodimeric enzyme complex with NOX4 displayed an identical cellular expression pattern and was also positively regulated by TSH. ROS may have various biological effects, depending on the site of production. Intracellular NOX4-p22(phox) localization suggests a role in cytoplasmic redox signaling, in contrast to the DUOX localization at the apical membrane that corresponds to an extracellular H(2)O(2) production. Increased NOX4-p22(phox) in cancer might be related to a higher proliferation rate and tumor progression but a role in the development of tumors has to be further studied and established in the future.
Insights
NADPH oxidase 4 (NOX4) is present in the thyroid and its levels increase in differentiated thyroid cancers. NOX4 generates reactive oxygen species (ROS) and may play a role in tumor progression.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- NADPH oxidase 4 (NOX4) is a key enzyme in reactive oxygen species (ROS) generation.
- The function and distribution of NOX4 in the thyroid gland are not fully understood.
- Previous studies in the thyroid focused on DUOX1/2 NOX systems.
Purpose of the Study:
- To investigate the presence, regulation, and function of NOX4 in normal and cancerous thyroid tissues.
- To determine the relationship between NOX4 expression, TSH, and ROS production in the thyroid.
- To elucidate the potential role of NOX4 in thyroid cancer development and progression.
Main Methods:
- Real-time PCR for NOX4 mRNA expression analysis.
- Western blotting and immunostaining for NOX4 and p22(phox) protein detection.
- Primary human thyroid cell culture to study TSH regulation and ROS generation.
Main Results:
- NOX4 mRNA and protein are expressed in normal thyroid tissue, with increased expression in differentiated thyroid cancers.
- Thyroid-stimulating hormone (TSH) regulates NOX4 expression and enhances NOX4-dependent ROS generation.
- NOX4 and its partner protein p22(phox) show distinct cellular localization, suggesting a role in cytoplasmic redox signaling.
Conclusions:
- NOX4 is present and regulated by TSH in the thyroid gland.
- Increased NOX4-p22(phox) expression in thyroid cancer may correlate with higher proliferation and tumor progression.
- Further research is needed to establish the specific role of NOX4 in thyroid tumorigenesis.
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