UOK 262 cell line, fumarate hydratase deficient (FH-/FH-) hereditary leiomyomatosis renal cell carcinoma: in vitro and in vivo model of an aberrant energy metabolic pathway in human cancer

被引:117
作者
Yang, Youfeng [1 ]
Valera, Vladimir A. [1 ]
Padilla-Nash, Hesed M. [2 ]
Sourbier, Carole [1 ]
Vocke, Cathy D. [1 ]
Vira, Manish A. [1 ]
Abu-Asab, Mones S. [3 ]
Bratslavsky, Gennady [1 ]
Tsokos, Maria [3 ]
Merino, Maria J. [3 ]
Pinto, Peter A. [1 ]
Srinivasan, Ramaprasad [1 ]
Ried, Thomas [2 ]
Neckers, Len [1 ]
Linehan, W. Marston [1 ]
机构
[1] NCI, Urol Oncol Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] NCI, Genet Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[3] NCI, Pathol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
UTERINE LEIOMYOMAS; MAMMALIAN-CELLS; MUTATIONS; GENE; TUMORS; TRANSLOCATION; FAMILIES; SPECTRUM;
D O I
10.1016/j.cancergencyto.2009.08.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Energy deregulation and abnormalities of tumor cell metabolism are critical issues in understanding cancer. Hereditary leiomyomatosis renal cell carcinoma (HLRCC) is an aggressive form of RCC characterized by germline mutation of the Krebs cycle enzyme fumarate hydratase (FH), and one known to be highly metastatic and unusually lethal. There is considerable utility in establishing preclinical cell and xenograft models for study of disorders of energy metabolism, as well as in development of new therapeutic approaches targeting of tricarboxylic acid (TCA) cycle enzyme deficient human cancers. Here we describe a new immortalized cell line, UOK 262, derived from a patient having aggressive HLRCC-associated recurring kidney cancer. We investigated gene expression, chromosome profiles, efflux bioenergetic analysis, mitochondrial ultrastructure, FH catabolic activity, invasiveness, and optimal glucose requirements for in vitro growth. UOK 262 cells have an isochromosome 1q recurring chromosome abnormality, i(1)(q10), and exhibit compromised oxidative phosphorylation and in vitro dependence on anaerobic glycolysis consistent with the clinical manifestation of HLRCC. The cells also display glucose-dependent growth, an elevated rate of lactate efflux, and overexpression of the glucose transporter GLUT I and of lactate dehydrogenase A (LDHA). Mutant FH protein was present primarily in edematous mitochondria, but with catalytic activity nearly undetectable. UOK 262 xenografts retain the characteristics of HLRCC histopathology. Our findings indicate that the severe compromise of oxidative phosphorylation and rapid glycolytic flux in UOK 262 are an essential feature of this TCA cycle enzyme-deficient form of kidney cancer. This tumor model is the embodiment of the Warburg effect. UOK 262 provides a unique in vitro and in vivo preclinical model for studying the bioenergetics of the Warburg effect in human cancer. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:45 / 55
页数:11
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