VHL tumor suppressor as a novel potential candidate biomarker in papillary thyroid carcinoma

被引:5
作者
Todorovic, Lidija [1 ]
Stanojevic, Boban [1 ,2 ,3 ]
机构
[1] Univ Belgrade, Lab Radiobiol & Mol Genet, Vinca Inst Nucl Sci, Natl Inst Republ Serbia, Belgrade, Serbia
[2] Kings Coll London, Dept Haematol Med, Div Canc Studies, Leukemia & Stem Cell Biol Team, London, England
[3] Great Ormond St Hosp Sick Children, Dept Cell & Gene Therapy, Virocell Biol, Zayed Ctr Res Rare Dis Children, London, England
来源
BIOMOLECULES AND BIOMEDICINE | 2023年 / 23卷 / 01期
关键词
Papillary thyroid cancer; papillary thyroid carcinoma (PTC); Von Hippel-Lindau (VHL); biomarker; risk stratification; tumor suppressor; VON-HIPPEL-LINDAU; ENDOTHELIAL GROWTH-FACTOR; REQUIRES DIRECT BINDING; RENAL-CELL CARCINOMA; GENE-PRODUCT; GERMLINE MUTATIONS; POOR-PROGNOSIS; RAS MUTATIONS; BETA-DOMAIN; IN-VITRO;
D O I
10.17305/bjbms.2022.7850
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Papillary thyroid carcinoma (PTC) is the most common type of endocrine cancer, with an increasing incidence worldwide. The treatment of PTC is currently the subject of clinical controversy, making it critically important to identify molecular markers that would help improve the risk stratification of PTC patients and optimize the therapeutic approach. The Von Hippel-Lindau (VHL) tumor suppressor gene has been implicated in tumorigenesis of various types of carcinoma and linked with their aggressive biological behavior. The role of VHL in the origin and development of PTC have only recently begun to be revealed. In this narrative review, we attempt to summarize the existing knowledge that implicates VHL in PTC pathogenesis and to outline its potential significance as a candidate molecular biomarker for the grouping of PTC patients into high and low risk groups.
引用
收藏
页码:26 / 36
页数:11
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