Dataset associated with the journal publication "Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer"
- 1. Endocrine Oncology Unit, Department of Endocrine and Metabolic Diseases, IRCCS Istituto Auxologico Italiano
- 2. Endocrine Oncology Unit, Department of Endocrine and Metabolic Diseases, IRCCS Istituto Auxologico Italiano; Department of Pathophysiology and Transplantation, University of Milan
- 3. Pathology Unit, IRCCS Istituto Auxologico Italiano
- 4. Division of Surgery, IRCCS Istituto Auxologico Italiano
- 5. Bioinformatics and Statistical Genomics Unit, IRCCS Istituto Auxologico Italiano; Department of Brain and Behavioral Sciences, University of Pavia
- 6. Endocrine Oncology Unit, Department of Endocrine and Metabolic Diseases, IRCCS Istituto Auxologico Italiano; Department of Medical Biotechnology and Translational Medicine, University of Milan
Description
Abstract: Oxidative stress (OS) can have an impact in the pathogenesis and in the progression of thyroid cancer. We investigated the levels of reactive oxygen species (ROS) in 50 malignant and benign thyroid lesions and 41 normal tissues, and correlated them with the thyroid differentiation score-TDS and the clinico-pathologic features. NOX4 expression, GPx activity and the genetic pattern of tumors were evaluated. In malignant and benign lesions, ROS generation and NOX4 protein expression were higher than in normal tissues. Follicular (FTCs) and anaplastic/poorly differentiated cancers had increased OS relative to papillary tumors (PTCs). Moreover, OS in FTCs was higher than in follicular adenomas. Mutated PTCs showed increased OS compared with non-mutated PTCs. In malignant tumors, OS was inversely correlated with TDS, and directly correlated with tumor stage and ATA risk. GPx activity was increased in tumors compared with normal tissues, and inversely correlated to OS. In conclusion, our data indicate that thyroid tumors are exposed to higher OS compared with normal tissues, while showing a compensative increased GPx activity. OS correlates with tumor aggressiveness and mutations in the MEK-ERK pathway in PTC. The inverse correlation between OS and TDS suggests that ROS may repress genes involved in thyroid differentiation.
This dataset of raw data cannot be made publicly available as it contains sensitive information, but may be made available to interested researchers on reasonable request at m.muzza@auxologico.it