Hypoxia-inducible Factor 2-Dependent Pathways Driving von Hippel-Lindau-Deficient Renal Cancer

被引:40
|
作者
Melendez-Rodriguez, Florinda [1 ,2 ]
Roche, Olga [3 ,4 ,5 ]
Sanchez-Prieto, Ricardo [3 ,4 ,6 ]
Aragones, Julian [1 ,2 ]
机构
[1] Autonomous Univ Madrid, Res Inst Princesa IP, Hosp Santa Cristina, Res Unit, Madrid, Spain
[2] Carlos III Hlth Inst, CIBER Enfermedades Cardiovasc, Madrid, Spain
[3] Univ Castilla La Mancha, CSIC, Unidad Asociada Biomed, Albacete, Spain
[4] Univ Castilla La Mancha, Fac Med, Dept Ciencias Med, Albacete, Spain
[5] Univ Castilla La Mancha, Ctr Reg Invest Biomed, Lab Oncol Mol, Unidad Med Mol, Albacete, Spain
[6] Univ Autonoma Madrid, CSIC, Dept Biol Canc, Inst Invest Biomed Alberto Sols, Madrid, Spain
来源
FRONTIERS IN ONCOLOGY | 2018年 / 8卷
关键词
Von Hippel-Lindau; hypoxia-inducible factors; hypoxia-inducible factor 2; kidney; renal cancer; clear cell renal cell carcinoma; DOMAIN-CONTAINING PROTEIN-1; ENDOTHELIAL GROWTH-FACTOR; TUMOR-SUPPRESSOR GENE; CELL CARCINOMA; C-MYC; HIF; EXPRESSION; HIF-2-ALPHA; METABOLISM; IDENTIFICATION;
D O I
10.3389/fonc.2018.00214
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The most common type of the renal cancers detected in humans is clear cell renal cell carcinomas (ccRCCs). These tumors are usually initiated by biallelic gene inactivation of the Von Hippel-Lindau (VHL) factor in the renal epithelium, which deregulates the hypoxia-inducible factors (HIFs) HIF1 alpha and HIF2 alpha, and provokes their constitutive activation irrespective of the cellular oxygen availability. While HIF1a can act as a ccRCC tumor suppressor, HIF2 alpha has emerged as the key HIF isoform that is essential for ccRCC tumor progression. Indeed, preclinical and clinical data have shown that pharmacological inhibitors of HIF2 alpha can efficiently combat ccRCC growth. In this review, we discuss the molecular basis underlying the oncogenic potential of HIF2 alpha in ccRCC by focusing on those pathways primarily controlled by HIF2 alpha that are thought to influence the progression of these tumors.
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页数:8
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