دورية أكاديمية

Fumarate Hydratase Deficiency in Renal Cancer Induces Glycolytic Addiction and Hypoxia-Inducible Transcription Factor 1α Stabilization by Glucose-Dependent Generation of Reactive Oxygen Species.

التفاصيل البيبلوغرافية
العنوان: Fumarate Hydratase Deficiency in Renal Cancer Induces Glycolytic Addiction and Hypoxia-Inducible Transcription Factor 1α Stabilization by Glucose-Dependent Generation of Reactive Oxygen Species.
المؤلفون: Sudarshan, Sunil, Sourbier, Carole, Hye-Sik Kong, Block, Karen, Romero, Vladimir A. Valera, Youfeng Yang, Galindo, Cynthia, Mollapour, Mehdi, Scroggins, Bradley, Goode, Norman, Min-Jung Lee, Gourlay, Campbell W., Trepel, Jane, Linehan, W. Marston, Neckers, Len
المصدر: Molecular & Cellular Biology; Aug2009, Vol. 29 Issue 15, p4080-4090, 11p
مصطلحات موضوعية: SMOOTH muscle tumors, RENAL cell carcinoma, GLYCOLYSIS, HYPOXEMIA, GLUCOSE, REACTIVE oxygen species, GENETIC transcription
مستخلص: Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an inherited cancer syndrome linked to biallelic inactivation of the gene encoding the tricarboxylic acid cycle enzyme fumarate hydratase (FH). Individuals with HLRCC are at risk to develop cutaneous and uterine leiomyomas and an aggressive form of kidney cancer. Pseudohypoxic drive-the aberrant activation of cellular hypoxia response pathways despite normal oxygen tension-is considered to be a likely mechanism underlying the etiology of this tumor. Pseudohypoxia requires the oxygen-independent stabilization of the α subunit of the hypoxia-inducible transcription factor (HIF-1α). Under normoxic conditions, proline hydroxylation of HIF-1α permits VHL recognition and subsequent targeting for proteasomal degradation. Here, we demonstrate that inactivating mutations of FH in an HLRCC-derived cell line result in glucose-mediated generation of cellular reactive oxygen species (ROS) and ROS-dependent HIF-1α stabilization. Additionally, we demonstrate that stable knockdown of FH in immortalized renal epithelial cells results in ROS-dependent HIF-1α stabilization. These data reveal that the obligate glycolytic switch present in HLRCC is critical to HIF stabilization via ROS generation. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:02707306
DOI:10.1128/MCB.00483-09