Moreover, FDG-PET is used for treatment PF-02341066 order planning and is used to evaluate

the response to therapy [1]. The SLC2A1 (also called glucose transporter type 1, GLUT1) gene is the primary glucose transporter gene in human lung cancer [2]. Hypoxia-inducible factor 1a (HIF-1a) controls oxygen delivery via angiogenesis and metabolic adaptation to hypoxia via glycolysis [3]. HIF-1a regulates SLC2A1 gene expression in cells that are subjected to hypoxic conditions [4]. Etomoxir concentration Many cellular proteins interact with or are under the control of HIF1-a. HIF-1a overexpression and enhanced transcriptional activity are linked to tumor initiation and progression. Indeed, a large number of clinicopathologic studies have confirmed that unlike mature normal tissues, HIF-1a is overexpressed in the cytoplasm and nuclei of 40%-80% of human carcinomas, including lung, breast, head and neck, endometrial cancers, melanomas, and sarcomas [5, 6]. Recently, Fu et al. [7] and Koukourakis et al. [8] showed that a HIF1A gene polymorphism affected HIF-1a protein expression. The expression of the downstream SLC2A1 and vascular endothelial growth Epigenetics inhibitor factor (VEGF) genes are regulated by a HIF1A-activated transcription pathway. VEGFA is the major mediator of angiogenesis and vascular permeability and transcription of this gene under hypoxic conditions

depends on HIF-1a induction. A C>T polymorphism at position 936 in the 3′ untranslated region of the VEGFA gene has been associated with

the plasma levels of VEGFA [9]. The T variant, which is linked to lower VEGFA levels, has been associated with colon cancer [10] and low FDG uptake [11]. These findings suggest Tau-protein kinase a potential role of the VEGFA 936C>T polymorphism for the variability of FDG uptake in tumor tissues. One important mammalian redox modulator is the bifunctional enzyme Redox factor-1 (Ref-1, also termed APEX1), that promotes transcriptional activation of HIF-1 or hypoxia inducible factor-like factor (HLF) by reducing C-terminal domain of HIF-1 or HLF [12], although the major role of this enzyme is DNA base excision repair [13]. Recently, APEX polymorphisms have been the focus of studies involving several different types of cancer, including colorectal [14], breast [15], and non-small cell lung cancer (NSCLC) [16]. These results suggested the involvement of APEX1 in the development of lung cancer. The proteins encoded by SLC2A1 and VEGFA are under the control of HIFA gene expression. An effect of these gene polymorphisms on glucose uptake to modify FDG-uptake could be influenced by the interaction of proteins in a common pathway. In this study, we have determined the impact of SLC2A1 polymorphisms on FDG-uptake (maximum standardized uptake value [SUVmax]) using a pathway-based approach with a combination of HIFA, APEX1, and VEGFA gene polymorphisms that might influence glucose uptake. Materials and methods 1.