Could Oxidative Stress Play a Role in the Development and Clinical Management of Differentiated Thyroid Cancer?

被引:15
作者
Kosciuszko, Maria [1 ]
Buczynska, Angelika [2 ]
Kretowski, Adam Jacek [1 ,2 ]
Poplawska-Kita, Anna [1 ]
机构
[1] Med Univ Bialystok, Dept Endocrinol Diabetol & Internal Med, PL-15274 Bialystok, Poland
[2] Med Univ Bialystok, Clin Res Ctr, PL-15274 Bialystok, Poland
关键词
thyroid cancer; oxidative stress; antioxidant capacity; cancer progression; LIPID-PEROXIDATION; FOLLICULAR VARIANT; DNA-DAMAGE; REDIFFERENTIATION; ANTIOXIDANTS; THERAPY; NODULES; REPAIR; BRAF;
D O I
10.3390/cancers15123182
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Increased oxidative stress (OS) has been implicated as a relevant risk factor for cancer development and progression. The incidence of differentiated thyroid cancer (DTC) has risen in several populations globally over the last few decades, accounting for approximately 1% of all cancer cases. Patients with DTC diagnosis have been characterized by an increased OS status, which is associated with a poorer prognosis. Therefore, assessing OS status could potentially be considered a useful tool in DTC clinical management. This measurement could be particularly valuable in personalizing treatment protocols and determining new potential medical targets. The purpose of this article is to evaluate research that examines the influence of OS on the progression of DTC and investigate the feasibility of utilizing OS measurements in DTC risk assessment. Gaining a comprehensive understanding of the correlation between carcinogenesis and OS, specifically in the DTC cases, can facilitate the development of novel therapeutic strategies. Increased oxidative stress (OS) has been implicated as a relevant risk factor for cancer progression. Furthermore, patients diagnosed with differentiated thyroid cancer (DTC) have been characterized by an increased OS status. Therefore, assessing OS status could potentially be considered a useful tool in DTC clinical management. This measurement could be particularly valuable in personalizing treatment protocols and determining new potential medical targets to improve commonly used therapies. A literature review was conducted to gather new information on DTC clinical management, with a particular focus on evaluating the clinical utility of OS. These meta-analyses concentrate on novel approaches that employ the measurement of oxidative-antioxidant status, which could represent the most promising area for implementing clinical management.
引用
收藏
页数:17
相关论文
共 128 条
[21]   Clinicopathological and molecular characterization of nine cases of columnar cell variant of papillary thyroid carcinoma [J].
Chen, Jey-Hsin ;
Faquin, William C. ;
Lloyd, Ricardo V. ;
Nose, Vania .
MODERN PATHOLOGY, 2011, 24 (05) :739-749
[22]   Identification of DPP4/CTNNB1/MET as a Theranostic Signature of Thyroid Cancer and Evaluation of the Therapeutic Potential of Sitagliptin [J].
Cheng, Sheng-Yao ;
Wu, Alexander T. H. ;
Batiha, Gaber El-Saber ;
Ho, Ching-Liang ;
Lee, Jih-Chin ;
Lukman, Halimat Yusuf ;
Alorabi, Mohammed ;
AlRasheedi, Abdullah N. ;
Chen, Jia-Hong .
BIOLOGY-BASEL, 2022, 11 (02)
[23]   BRAF and TERT promoter mutations: clinical application in thyroid cancer [J].
Chung, Jae Hoon .
ENDOCRINE JOURNAL, 2020, 67 (06) :577-584
[24]   Recent Insights into the Cell Biology of Thyroid Angiofollicular Units [J].
Colin, Ides M. ;
Denef, Jean-Francois ;
Lengele, Benoit ;
Many, Marie-Christine ;
Gerard, Anne-Catherine .
ENDOCRINE REVIEWS, 2013, 34 (02) :209-238
[25]   Known and novel roles of the MET oncogene in cancer: a coherent approach to targeted therapy [J].
Comoglio, Paolo M. ;
Trusolino, Livio ;
Boccaccio, Carla .
NATURE REVIEWS CANCER, 2018, 18 (06) :341-358
[26]   Noncanonical roles of p53 in cancer stemness and their implications in sarcomas [J].
Curylova, Lucie ;
Ramos, Helena ;
Saraiva, Lucilia ;
Skoda, Jan .
CANCER LETTERS, 2022, 525 :131-145
[27]   Genetically altered mice to evaluate glutathione homeostasis in health and disease [J].
Dalton, TP ;
Chen, Y ;
Schneider, SN ;
Nebert, DW ;
Shertzer, HG .
FREE RADICAL BIOLOGY AND MEDICINE, 2004, 37 (10) :1511-1526
[28]   Direct and indirect antioxidant properties of inducers of cytoprotective proteins [J].
Dinkova-Kostova, Albena T. ;
Talalay, Paul .
MOLECULAR NUTRITION & FOOD RESEARCH, 2008, 52 :S128-S138
[29]   Mechanisms of free radical-induced damage to DNA [J].
Dizdaroglu, Miral ;
Jaruga, Pawel .
FREE RADICAL RESEARCH, 2012, 46 (04) :382-419
[30]   Oxidative stress values of tumor core, edge, and healthy thyroid tissue in thyroid masses [J].
Dogan, Remzi ;
Dogan, Elif Ece ;
Guler, Eray Metin ;
Senturk, Erol ;
Yenigun, Alper ;
Celik, Ismail ;
Aksoy, Fadlullah ;
Ozturan, Orhan .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2021, 278 (08) :2953-2960